Publications

308. Spatially Tweaked Amide Directing Group Enables High-Turnover Pd Catalysts for Site-Selective Remote C−H Arylation

Sivaraj, C.; Gandhi, T.; Maiti, D.

ACS Catal., 2025, (ASAP)

307. Consecutive multiphoton mediated defluorinative amination of fluoroarenes

Saha, A.;† Roy, M.;† Maji, S.; Rana, G.; Maiti, D.; Adhikari, D.

J. Am. Chem. Soc., 2025, (ASAP)

306. Scalable photoinduced cycloaddition for synthesis of biorelevant oxazoles

Saha, A.; Bianchi, M.; Casali, E.; Maiti, D.

Org. Lett., 2025, (ASAP)

305. Harnessing C–H acetoxylation: a gateway to oxygen-enriched organic frameworks

Grover, J.; Dutta, B.; Ghosh, D.; Shee, P. K.; Maiti, S.; Werz, D. B.; Maiti, D.

Chem. Sci., 2025, (ASAP)

304. Metal-catalysed non-directed C(sp2)–H bond activation

Agrawal, S. K.;† Porey, S.;† Bairagi, Y.;† Maiti, S.; Bissember, A. C.; Maiti, D.

Chem. Soc. Rev., 2025, (ASAP)

303. Copper(II) triflate/Vitamin-C Promoted Modified Morita-Baylis-Hillman Annulations: A Facile Route to Fluorescent Cyclopentene Derivatives

Azad, S. A.; Barik, P.; Samanta, J.; Sepay, N.; Sebastian, A. T.; Ghara, S.; Giri, S.; Molla, M. R.; Maiti, D.; Samanta, S.

Chem. Eur. J., 2025, (ASAP)

302. Synthesis of Lactones and Lactams by C(sp3)–H bond Functionalization

Premkumar, E.; Sreedharan, R.; Ghosh, P.; Pal, T.; Maiti, D.; Gandhi, T.

Chem. Soc. Rev., 2025, (ASAP)

301. Remote meta-C−H α-Fluoro-alkenylation of Arenes Using gem Difluoroalkenes

Bairagi, Y.;† Porey, S.;† Mahato, I.; Maiti, D.

ACS Catal., 2025, 15, 7536

300. Generating Pd-catalyzed δ C‒H chalcogenation of aliphatic picolinamides: systematically decreasing the bias

Sinha, S. K.; Gholap, A.; Yazhinimuthu, C. M.; Pal, A.; Kapdi, A. R.; Maiti, D.

Chem. Sci., 2025, 16, 7936

299. Modular Approach for Photoinduced Cycloaddition Enabling the Synthesis of Diverse Bioactive Oxazoles

Saha, A.; Casali, E.; Ghosh, A.; Maiti, D.

Org. Lett., 2025, 27, 2811

298. Cooperative Ligand Enabled Facile Synthesis of γ-C(sp3)−H Alkenylated Aliphatic Amides: A Comprehensive Protocol to Free N−H Tolerance

Dutta, S.; Kumar, N.; Islam, M.; Ali, W.; Gupta, P.; Maiti, D.

ACS Catal., 2025, 15, 5295

297. Pallada-Electrocatalysis Enables Distal Regioselective and Atroposelective Olefination Reactions

Panja, S.; Pan, A.; Biswas, S.; Das, C.; Guha, A.; Nimje, R. Y.; Dhar, T. G. M.; Gupta, A.; Mathur, A.; Dutta, A.; Roy, L.; Maiti, D.

Angew. Chem. Int. Ed., 2025, 64, e202422876

296. Palladium Catalyzed Regioselective Distal C (sp2)–H Functionalization

Chauhan, R. S.; Bairagi, Y.; Desai, O.; Kowalczyk, R.; Maiti, D.

ChemComm, 2025, 61, 4293

295. Site-Selective Remote C4-Amination of 1-Naphthamides via Palladium-SET Catalysis

Sivaraj, C.; Pradhan, S.; Gandhi, T.; Maiti, D.

Org. Lett., 2025, 27, 1650

294. Unified Approaches in Transition Metal Catalyzed C(sp3)-H Functionalizations: Recent Advances and Mechanistic Aspects

Grover, J.; Sebastian, A. T.; Maiti, S.; Bissember, A. C.; Maiti, D.

Chem. Soc. Rev., 2025, 54, 2006

293. Pd-Catalyzed Skeletal Rearrangement via C(sp³)-C(sp³) Activation to Access α,β-Unsaturated δ/γ-Lactone

Manna, K.;† Maji, S.;† Sharma, A.; Kumar, N.; Gupta, P.; Maiti, D.

Angew. Chem. Int. Ed., 2025, 64, e202423175

292. Palladium-Catalyzed Para-Selective Arylation of 1‑Naphthamide

Pradhan, S.; Dutta, U.; Biswas, J. P.; Elsaid, M.; Ge, H.; Maiti, D.

Org. Lett., 2024, 26, 10946

291. Rhodium-Catalyzed Meta-C−H Arylation of Arenes with VariedLinker Lengths: Bridging Catalytic Selectivity with StructuralDiversity

Mandal, A.; Biswas, J. P.; Maiti, D.

Angew. Chem. Int. Ed., 2024, 64, e202419954

290. Facile Construction of Distal and Diversified Tertiary and Quaternary Stereocenters

Liu, C.; Ge, R.; Chen, J.; Guo, H.; Bartholome, T. A.; Maiti, D.; Ge, H.

Proc. Natl. Acad. Sci. U.S.A., 2024, 121, e2408541121

289. Taming CO2•– via synergistic triple catalysis in anti-Markovnikov hydrocarboxylation of alkenes

Ghosh, P.;† Maiti, S.;† Malandain, A.; Raja, D.; Loreau, O.; Maity, B.; Roy, T. K.; Audisio, D.; Maiti, D.

J. Am. Chem. Soc., 2024, 146, 30615

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288. Synthesis of β-(Hetero)aryl Ketones via Ligand-Enabled Nondirected C-H Alkylation

Bairagi, Y.;† Porey, S.;† Vummaleti, S. V. C.; Zhang, X.; Lahiri. G. K.; Maiti, D.

ACS Catal., 2024, 14, 15654

287. A Modular Approach for Accessing 3D Heterocycles via 1,2-Dicyanation of Planar N-Heteroarenes

Pradhan, S.; Maiti, S.; Dutta, S.; Russell, C. A.; Tyagi, S.; Maiti, D.

Angew. Chem. Int. Ed., 2024, e202412979

286. Substrate-Directed C(sp3)-H Borylation via Transition Metal Catalysis: Expanding the Toolbox for C-H Functionalization

Thalakottukaraa, D. D.; Sekara, M.; Mandal, A.; Gandhi, T.; Maiti, D.

Catal. Sci. Technol., 2024, (ASAP)

285. Hydrogen Bonding Template Enables Remote Meta-C–H Alkenylation of Nitroarenes with Electron-Deficient Alkenes

Dutta, B.; Mahajan, M.; Ghosh, A.; Dajek, M.; Kowalczyk, R.; Mondal, B.; Ge, H.; Maiti, D.

Nat. Commun., 2024, 15, 7543

284. Metal-free Borylation of α-Naphthamides and Phenylacetic Acid Drug

Maji, S.; Rawal, P.; Ghosh, A.; Pidiyar, K.; Al-Thabaiti, S. A.; Gupta, P.; Maiti, D.

JACS Au., 2024, (ASAP)

283. Deuteration and Tritiation of Pharmaceuticals by Non-Directed Palladium Catalyzed C–H Activation in Heavy and Super-Heavy Water

Teja, C.; Kolb, S.; Colonna, P.; Grover, J.; Garcia-Argote, S.; Lahiri, G. K.; Pieters, G.; Werz. D. B.; Maiti, D.

Angew. Chem. Int. Ed., 2024, e202410162

282. Pd-catalyzed regioselective activation of C(sp2)-H and C(sp3)-H bonds

Ali, W.; Oliver, G. A.; Werz, D. B.; Maiti, D.

Chem. Soc. Rev., 2024, (ASAP)

281. Ligand controlled orthogonal selectivity between δ and γ positions of long chain picolinamides

Sinha, S. K.;† Goswami, N.;† Li, Y.;† Maji, S.; Raja, D.; Sarala, A. S.; Guin, S.; Paton. R. S.; Maiti, D.

ACS Catal. 2024, 14, 12681

280. Selective cross-hydrodimerization of alkenes

Maiti, S.; Maiti, D.

Nat. Synth., 2024, (ASAP)

279. Palladium-Catalyzed Remote C–H Functionalization: Non-Covalent Interactions and Reversibly Bound Templates

Sebastian, A. T.;† Maji, S.;† Rajashekhar, M.; Maiti, S.; Kowalczyk, R.; Maiti, D.

Angew. Chem. Int. Ed., 2024, e202410806

278. Expedited Proton Relay in Enzyme-Inspired Cobaloximes Facilitates Organic Transformations

Panja, S.; Nandi, C.; Guria, S.; Pan, A.; Das, C.; Das, S.; Ghorai, S.; Dutta, A.; Maiti, D.

Chem. Eur. J., 2024, 30, e202401785

277. Tandem Dehydrogenation-Olefination-Decarboxylation of Cycloalkyl Carboxylic Acids via Multifold C-H Activation

Pal, T.; Ghosh, P.; Islam, M., Guin, S.; Maji, S.; Dutta, S.; Das, J.; Ge, H.; Maiti, D.

Nat. Commun., 2024, 15, 5370

276. Enantiodivergent synthesis of isoindolones catalysed by a Rh(III)-based artificial metalloenzyme

Mukherjee, P.;† Sairaman, A.;† Deka, H. J.; Jain, S.; Mishra, S. K.; Roy, S.; Bhaumik, P.; Maiti, D.

Nat. Synth., 2024, 3, 835

275. A Scalable Continuous Photo-Flow Protocol for Anaerobic Oxidative Cleavage of Styrenes

Prakash, G.;† Grover, J.;† Pathak, P.;† Mittal, A. K.; Balasubramaniam, P.; Maiti, D.

React. Chem. Eng., 2024, 9, 1032

274. Surpassing the Limited Coordination Affinity of Native Amides by Introducing Pyridone-Pd-AgOAc Cluster to Promote Distal γ-C(sp3)-H Arylation

Goswami, N.; Kumar, N.; Gupta, P.; Maiti, D.

ACS Catal. 2024, 14, 3798–3811

273. Mizoroki–Heck-type transformations in natural product synthesis: case studies in carbopalladation and forging all-carbon quaternary stereocenters

Fuller, R. O.; Maiti, D.; Bissember, A. C.

Chem Catal., 2024, 100921

272. Harnessing the “Methyl Effect” in the Development of Novel Meta-directing Template for C–H Cyanation

Bhattacharya, T.;† Teja, C.;† Kumar, N.; Bhagat, K. K.; Lahiri, G. K.; Gupta, P.; Tyagi, S.; Maiti, D.

ACS Catal. 2024, 14, 2216–2228

271. Light-induced Pd catalyst enables C(sp2)–C(sp2) cross-electrophile coupling bypassing the demand for transmetalation

Maiti, S.; Ghosh, P.; Raja, D. K.; Ghosh, S.; Chatterjee, S.; Sankar, V.; Roy, S.; Lahiri, G. K.; Maiti, D.

Nat. Catal., 2024, 7, 285

Highlighted in Synfacts

270. Highly scalable photoinduced synthesis of silanols via untraversed pathway for chlorine radical (Cl•) generation

Saha, A.; Ali, W.; Werz, D. B.; Maiti, D.

Nat. Commun., 2023, 14, 8173

269. Combinatorial Ligand Assisted Simultaneous Control of Axial and Central Chirality in Highly Stereoselective C-H Allylation

Bhattacharya, T.; Ghosh, S.; Dutta, S.; Guin, S.; Ghosh, A.; Ge, H.; Sunoj, R. B.; Maiti, D.

Angew. Chem. Int. Ed. 2023, 63, e20231011

268. Photo-Catalyzed Acyl Azolium Promoted Selective α-C(sp3)–H Acylation of Acetone via HAT: Access to Thermodynamically Less Favoured (Z)-α,β-Unsaturated Ketones

Sivaraj, C.; Maiti, D.; Gandhi, T.

Chem. Eur. J., 2024, e202303626.

267. Urea Promoted Neat Synthesis of Fused Dihydroisoquinolines and Disubstituted Pyridines: A Mechanistic Observation with Molecular Sensing Studies

Azad, A. Sk.; Bera, A.; Samanta, J.; Sepay, N.; Jana, R.; Pal, C. K.; Molla, M. R.; Maiti, D.; Samanta, S.

Chem. Eur. J., 2024, e202303287

266. Photoinduced [3+2] Cycloaddition of Carbenes and Nitriles: A Versatile Approach to Oxazole Synthesis

Saha, A.; Sen, C.;† Guin, S.;† Das, C.; Maiti, D.; Sen, S.; Maiti, D.

Angew. Chem. Int. Ed, 2023, 62, e20230891

Highlighted in ChemistryViews, Highlighted in Org. Process Res. Dev., Highlighted in Synfacts

265. Unveiling catalyst-free electro-photochemical reactivity of aryl diazoesters and facile synthesis of oxazoles, imide-fused pyrroles and tetrahydro-epoxy-pyridines via carbene radical anion

Maiti, D.; Saha, A.; Guin, S.; Maiti, D.; Sen, S.

Chem. Sci., 2023, 14, 6216

264. Non-Directed C-H/C-F Coupling for the Synthesis of α-Fluoro Olefinated Arenes

Porey, S.; Bairagi, Y.; Guin, S.; Zhang, X.; Maiti, D.

ACS Catal. 2023, 13, 14000–14011

Highlighted in Synfacts

263. Energy-efficient CO2/CO interconversion by homogeneous copper-based molecular catalysts

Guria, S.; Dolui, D.; Das, C.; Ghorai, S.; Vishal, V.; Maiti, D.; Lahiri, G. K.; Dutta, A.

Nat. Commun., 2023, 14, 6859

262. Transition-metal catalyzed C‒H activation as a means of synthesizing complex natural products

Sinha, S. K.;† Ghosh, P.;† Jain, S.; Maiti, S.; Al-Thabati, S. A.; Alshehri, A. A.; Mokhtar, M.; Maiti, D.

Chem. Soc. Rev., 2023, 52, 7461-7503

261. Directing Group Assisted para-Selective C-H Alkynylation of Unbiased Arenes Enabled by Rhodium Catalysis

Dutta, U.;† Prakash, G.;† Devi, K.; Borah, K.; Zhang, X.; Maiti, D.

Chem. Sci., 2023, 14, 11381

260. Palladium-catalyzed cascade reactions initiated with directed activation of unactivated sp3 C–H bonds

Ge, R.; Herington, F.; Mangawang, A.; Maiti, D.; Ge, H.

Tet. Chem., 2023, 7, 100046

259. Highly scalable and inherently safer preparation of di, tri and tetra-nitrate esters using continuous flow chemistry

Mittal, A. K.;† Pathak, P.;† Prakash, G.;† Maiti, D.

Chem. Eur. J., 2023, 29, e202301662.

258. Deciphering the Mechanistic Insights of Temporary Directing Group Assisted meta-Alkenylation of Complex Biaryl Systems

Goswami, N.;† Kumar, N.;† Bag, S.; Gupta, P.; Maiti, D.

ACS Catal., 2023, 13, 11091

257. Access to Unsaturated Bicyclic Lactones by Overriding Conventional C(sp3)-H Site Selectivity

Das, J.; Ali, W.; Ghosh, A.;† Pal, T.;† Mandal, A.;† Teja, C.; Dutta, S.; Pothikumar, R.; Ge, H.; Zhang, X.; Maiti, D.

Nat. Chem., 2023, 15, 1626

Nature Blog

Highlighted in Research Matters, Selected as Synfact of the Month Feb'24

Covered in the April issue of Synform

256. A base metal catalyst for indirect hydrogenation of CO2

Grover, J.; Maji, S.; Teja. C.; Al-Thabaiti, S. A.; Mokhtar, M.; Lahiri, G. K.; Maiti, D.

ACS Org. Inorg. Au, 2023, 3, 299

255. Palladium-catalyzed amide-directed ligand free C8-olefination of 1-naphthamides for the synthesis of 2,3-dihydro-1H-benzo[de]isoquinolin-1-ones

Maji, S.;† Pradhan, S.;† Pidiyar, K.; Maiti, S.; Al-Thabaiti, S. A.; Maiti, D.

Adv. Synth. Catal., 2023, 366, 838

254. Continuous flow synthesis of tert-butyl nitrite and its applications as nitrating agent

Mittal, A. K.;† Prakash, G.;† Pathak, P.;† Dutta, B.; Ahalyan, N.; Maiti, S.; Maiti, D.

Org. Process Res. Dev., 2023 (ASAP)

253. Simplifying the Synthesis of Non-proteinogenic Amino Acids via Palladium Catalysed (delta)-Methyl C-H Olefination of Aliphatic Amines and Amino Acids

Bhattacharya, T.; Baroliya, P. K.; Al-Thabaiti, S. A.; Maiti, D.

JACS Au, 2023, 3, 1975

252. Photoinduced meta-Selective C-H Oxygenation of Arenes

Ali, W.;† Saha, A.;† Ge, H.; Maiti, D.

JACS Au, 2023, 3, 1790

251. The Evolution of Directing-Group Strategies for C(sp3)-H Activation

Das, J.;† Ali, W.;† Maiti, D.

Trends in Chemistry, 2023, 5, 551

250. Site-Selective C–H Functionalization of Carbazoles

Elsaid, M.;† Ge, R.;† Liu, C.; Maiti, D.; Ge, H.

Angew. Chem. Int. Ed, 2023,62, e202303110

249. Metal-free photoinduced hydrogen atom transfer assisted C(sp3)–H thioarylation

Grover. J.;† Prakash. G.;† Teja. C.; Lahiri. G.K.; Maiti. D.

Green Chem, 2023, 25, 3431

248. Structural authentication of intermediates of mechanistic significance in palladium- and nickel-catalysed cross-couplings: case studies

Olding, A.; Ho, C. C.; Maiti, D.; Bissember, A. C.

ChemComm, 2023, 59, 5144

247. Alkene/Alkane Cross-Dehydrogenative Coupling for C(sp2)-C(sp3) Bond Formation

Ali, W.; Guin, S.; Maiti, D.

Science of Synthesis (SOS) 2023

246. The reaction of NOBF4 with antimony(III) corroles: fluoride binding to antimony and regioselective nitration of the macrocycle

Mondal, S.; Pain, T.; Mandal, A.; Maiti, D.; Kar, S.

Appl. Organomet. Chem., 2023, e7088

245. Free amine and alcohol as the director for regioselective C(sp2)-H bond functionalization

Keshri, R.;† Rana, D.;† Saha, A.; Al-Thabaitid, S. A.; Alshehrid, A. A.; Bawaked, S. M.; Maiti, D.

ACS Catal., 2023, 13, 4500

244. Transition metal catalyzed C–H functionalization through electrocatalysis

Baroliya, P. K.; Dhaker, M.; Panja, S.; Al-Thabaiti, S. A.; Albukhari, S. M.; Alsulami, Q. A.; Dutta, A.; Maiti, D.

ChemSusChem, 2023, e202202201

243. Mechanism and Origins of Site-Selectivity of Template-Directed C-H Insertion of Quinolines

Fernandez, G. E.; Maiti, D.; Tantillo, D. J.

Chem. Eur. J., 2023, e202300124

242. Enroute Sustainability: Metal Free C-H bond Functionalisation

Roy, S.; Panja, S.; Sahoo, S. R.; Chatterjee, S.; Maiti, D.

Chem. Soc. Rev., 2023, 52, 2391

241. Enantioselective Annulation Reactions Through C(sp2)-H Activation with Chiral CpxM(III) Catalysts

Achar, T. K.; Al-Thabaiti, S. A.; Mokhtar, M.; Maiti, D.

Chem Catal., 2023, 3, 100575

240. 5-Methyl-3-nitro-2(1H)-pyridinone

Pal, T.; Maiti, D.

Encyclopedia of Reagents for Organic Synthesis (EROS) 2023

239. Benzylic Alcohol Oxidation using Copper Oxide/ZincOxide/Zirconia Nanocomposite Catalysts

Mokhtar, M.;† Panja, S.;† Alshehri, A.; Halawani,W.; Maiti, D.

Chem Asian J., 2023, 18, e2022012

238. Distal meta-alkenylation of formal amines enabled by catalytic use of hydrogen-bonding anionic ligands

Goswami, N.;† Sinha, S. K.;† Mondal, P.; Adhya, S.; Datta, A.; Maiti, D.

Chem, 2023, 9, 989

237. Transition Metal Catalyzed Remote C-H Activation: A New Direction Towards Site-Selective Chemical Reactions

Das, J.; Maiti, D.

AsiaChem, 2022 (ASAP)

236. Synthesis of picramide using nitration and ammonolysis in continuous flow

Mittal, A. K.;† Prakash, G.;† Pathak, P.;† Maiti, D.

Chem Asian J., 2023, 18, e202201028

235. Native Functional Group Directed Distal C(sp3)-H Activation of Aliphatic Systems

Saha, S.; Das, J.; Al-Thabaiti, S. A.; Albukhari, S. M.; Alsulami, Q. A.; Maiti, D.

Catal. Sci. Technol., 2023, 13, 11

234. Cluster Preface: Chemical Synthesis and Catalysis in India

Maiti, D.; Mukherjee, S.

Synlett., 2023, 34, 493

233. Transition Metal Pincer Complexes: A Series of Potential Catalysts in C−H Activation Reactions

Kasera, A.; Biswas, J. P.; Alshehri, A. A.; Al-Thabaiti, S. A.; Mokhtar, M.; Maiti, D.

Coord. Chem. Rev., 2023, 475, 214915

232. Synthesis of CTA and DNAN using flow chemistry

Mittal, A. K.;† Prakash, G.;† Pathak, P.;† Maiti, D.

Asian J. Org. Chem., 2022,11, e202200444

231. Recent Advances in Transition-Metal Mediated Trifluoromethylation Reactions

Mandal, D.;† Maji, S.;† Pal, T.;† Sinha, S. K.; Maiti, D.

ChemComm, 2022, 58, 10442

230. Substrate-Rhodium Cooperativity in Photoinduced ortho-Alkynylation of Arenes

Saha, A.; Ghosh, A.; Guin, S.; Panda, S.; Mal, D. K.; Majumdar, A.; Akita, M.; Maiti, D.

Angew. Chem. Int. Ed., 2022, 61, e202210492

229. Pd Catalyzed Dual-γ-1,1-C(sp3)-H Activation of Free Aliphatic Acids With Allyl-O Moieties

Das, J.; Pal, T.; Ali, W.; Sahoo, S. R.; Maiti, D.

ACS Catal., 2022, 12, 11169

228. Book Chapter: Investigation on High-Valent Iron Complex Mediated Organic Transformations: Reactivity and Mechanistic Impact

Book Title: Advances in Inorganic Chemistry (AINC) Vol. 81: Inorganic Chemistry in India

Roy, T. K.;† Suresh, A.;† Sinha, A.;† Biswas, J. P.; Maiti, D. Edited by: van Eldik, R.; Chatterjee, D.

Elsevier, 2022.

227. Photo-Excited Nickel-Catalyzed Silyl-Radical-Mediated Direct Activation of Carbamoyl Chlorides To Access (Hetero)aryl Carbamides

Maiti, S.;† Roy, S.;† Ghosh, P.; Kasera, A.; Maiti, D.

Angew. Chem. Int. Ed., 2022, 61, e202207472

226. Exploring cobalt-histidine complex for a wide-ranging colorimetric O2 detection

Saini, A.; Rai, S.; Maiti, D.; Dutta, A.

ACS Omega, 2022, 7, 27734

225. Non-Directed Pd-Catalysed Electrooxidative Olefination of Arenes

Panja, S.; Ahsan, S.; Pal, T.; Kolb, S.; Ali, W.; Sharma, S.; Das, C.; Grover, J.; Dutta, A.; Werz, D. B.; Paul, A.; Maiti, D.

Chem. Sci., 2022,13, 9432

224. Transition-Metal-Catalyzed C−H Bond Alkylation Using Olefins: Recent Advances and Mechanistic Aspects

Mandal, D.; Roychowdhury, S.; Biswas, J. P.; Maiti, S.; Maiti, D.

Chem. Soc. Rev., 2022, 51, 7358

223. Expanding chemical space by para-C-H arylation of arenes

Maiti, S.; Li, Y.; Sasmal, S.; Guin, S.; Bhattacharya, T.; Lahiri, G. K.; Paton, R. S.; Maiti, D.

Nat. Commun., 2022, 13, 3963

222. An Unprecedented Valorisation of Marble Slurry Waste Material as Solid Support for Palladium-Catalysed Heck and Suzuki Reactions

Chopra, J.; Dayma, V.; Mandal, A.; Baroliya, P. K.; Maiti, D.

ChemistrySelect, 2022, 7, e20220092

221. Dual Ligand Enabled Non-Directed C−H Chalcogenation of Arenes and Heteroarenes

Sinha, S. K.;† Panja, S.;† Grover, J.;† Hazra, P. S.; Pandit, S.; Bairagi, Y.; Zhang, X.; Maiti, D.

J. Am. Chem. Soc., 2022, 144, 12032

220. Recent developments in first-row transition metal complex-catalyzed CO2 hydrogenation

Das, C.; Grover, J.; T.; Das, A.; Maiti, D.; Dutta, A.; Lahiri, G. K.

Dalton Trans., 2022, 51, 8160

219. C−H Methylation Using Sustainable Approaches

Agrawal, I.;† Prakash, G.;† Al-Thabaiti, S. A.; Mokhtar, M.; Maiti, D.

Catalysts., 2022, 12, 510

218. Ligand-promoted palladium-catalyzed β-methylene C−H arylation of primary aldehydes

Yang, K.; Li, Z.; Liu, C.; Li, Y.; Hu, Q.; Elsaid, M.; Li, B.; Das, J.; Dang, Y.; Maiti, D.; Ge, H.

Chem. Sci., 2022, 13, 5938

217. Book Chapter: Cascade Reactions, Unity is Strength

Book Title: Synthetic approaches to nonaromatic nitrogen heterocycles vol. III

Casali, E.; Saraci, E.; Othman, S. T.; Zanoni, G.; Maiti, D. Edited by: Phillips, A. M. F.

Wiley-VCH, 2022

216. Directing Group Assisted Rhodium Catalyzed meta-C-H Alkynylation of Arenes

Sasmal, S.;† Prakash, G.;† Dutta, U.;† Laskar, R.; Lahiri, G. K.; Maiti, D.

Chem. Sci., 2022, 13, 5616

215. Modern Palladium-Catalyzed Transformations Involving C–H Activation and Subsequent Annulation

Thombal, R. S.;† Rubio, P. Y. M.;† Lee, D.; Maiti, D.; Lee, Y. R.

ACS Catal., 2022, 12, 5217

214. C-H deuteration of organic compounds and potential drug candidates

Prakash, G.; Paul, N.; Oliver, G. A.; Werz, D. B.; Maiti, D.

Chem. Soc. Rev., 2022, 51, 3123

213. Rh-catalyzed arene distal meta- and para-C-H functionalization

Ali, W.; Prakash, G.; Al-Thabaiti, S. A.; Mokhtar, M.; Maiti, D.

Edited by: Maiti, D.

Wiley-VCH, 2022

212. Intra- and inter-molecular carbene and nitrene insertion by metalloenzymes into C-H bond

Mukherjee, P.; Jain, S.; Al-Thabaiti, S. A.; Mokhtar, M.; Maiti, D.

Edited by: Maiti, D.

Wiley-VCH, 2022

211. C−H Activation: A Strategic Approach toward lactams using Transition metals

Dutta, S.;† Chatterjee, S.;† Al-Thabaiti, S. A.; Bawaked, S.; Mokhtar, M.; Maiti, D.

Chem. Catal., 2022, 2, 1046

210. Ene-Reductase: A Multifaceted Biocatalyst in Organic Synthesis

Roy, T. K.; Sreedharan, R.; Ghosh, P.; Gandhi, T.; Maiti, D.

Chem. Eur. J., 2022, 28, e202103949

209. Traditional and sustainable approaches for the construction of C-C bonds by harnessing C-H arylation

Grover, J.;† Prakash, G.;† Goswami, N.; Maiti, D.

Nat. Commun., 2022, 13,1085

208. Sustainable C-H functionalizations under ball-milling, microwave-irradiation and aqueous media

Laskar, R.;† Pal, T.;† Bhattacharya, T.; Maiti, S.; Akita, M.; Maiti, D.

Green Chem., 2022, 24, 2296

207. Pd-catalysed C-H functionalisation of free carboxylic acids

Dutta, S.; Bhattacharya, T.; Geffers, F. J.; W.; Bürger, M.; Maiti, D.; Werz, D. B

Chem. Sci., 2022, 13, 2551

206. An Atom Economical Approach for Enantioselective Cross Dehydrogenative Coupling

Das, J.; Maiti, D.

Chem. Catal., 2022, 2, 3

205. Strategies to Transform Remote C(sp3)-H bonds of Amino Acid Derivatives

Sen, S.; Das, J.; Maiti, D.

Tet. Chem., 2022, 1, 100005

204 .Emergence of Pyrimidine as meta-Directing Group: Journey from Weak to Strong Coordination in Diversifying meta-C−H Functionalization

Dutta, U.; Maiti, D.

Acc. Chem. Res., 2022, 55, 354

203. Toolbox for Distal C-H Bond Functionalizations in Organic Molecules

Sinha, S. K.; Guin, S.; Maiti, S.; Biswas, J. P.; Porey, S.; Maiti, D.

Chem. Rev., 2022, 122, 5682

202. Photoinduced Regioselective Olefination of Arenes at Proximal and Distal Sites

Saha, A.;† Guin, S.;† Ali, W.; Bhattacharya, T.; Sasmal, S.; Goswami, N.; Prakash, G.; Sinha, S. K.; Chandrashekar, H. B.; Panda, S.; Anjana, S. S.; Maiti, D.

J. Am. Chem. Soc., 2022, 144, 1929 , (This paper appears in synfacts contribution)

201. Group 6 transition metal-based molecular complexes for sustainable catalytic CO2 activation

Rajeshwaree, B.; Ali, A.; Mir, A. Q.; Grover, J.; Lahiri, G. K.; Dutta, A.; Maiti, D.

Catal. Sci. Technol., 2022, 12, 390

200. Catalytic C−H activation via four-membered metallacycle intermediate

Bhagat, K. K.; Biswas, J. P.; Dutta, S.; Maiti, D.

Helv. Chim. Acta., 2022, 105, e202100192

A simpler way to perform C–H methylation

Maiti, D.

Chemistry World, 2021

199. Supramolecular Interactions in Distal C – H Activation of (Hetero)arenes

Biswas, J. P.; Maiti, D.

Wiley-VCH, 2021

198. Direct C-E (E = boron, halogen, oxygen) bond formation through C-H activation

Goswami, N.; Mohan, R.; Maiti, D.

Comprehensive Organometallic Chemistry IV, Elsevier, 2021

197. Weinreb Amide as a Multifaceted Directing Group in C-H Activation

Das, J.; Maiti, D.

Wiley-VCH, 2021

196. Mechanistic Insights on Palladium-Catalyzed C(sp 2 )–H functionalization from Theoretical Perspective

Zhang, X.; Maiti, D.

Wiley-VCH, 2021

195. Recent Advances in the Incorporation of CO2 for C-H and C-C bond Functionalization

Pimparkar, S.; Dalvi, A. K.; Koodan, A.; Maiti, S.; Al-Thabaiti, S. A.; Mokhtar, M.; Dutta, A.; Lee, Y. R.; Maiti, D.

Green Chem., 2021, 23, 9283

194. Recent developments in hydrodecyanation and decyanative functionalization reaction

Paul, N.; Patra, T.; Maiti, D.

Asian J. Org. Chem., 2021, 10, 1

193. Editing the Skeletal Structure of Arenes via Transition Metal Catalyzed Decarbonylation Methodology

Sinha, S. K.; Roy, T. K.; Modak, A.; Maiti, D.

Chem. Rec., 2021, 21, 1

192. Ligand-redox assisted nickel catalysis toward stereoselective synthesis of (n+1)-membered cycloalkanes from 1,n-diols with methyl ketones

Bains, A. K.; Kundu, A.; Maiti, D.; Adhikari, D.

Chem. Sci., 2021, 12, 14217

191. Transition Metal Catalyzed C–H Bond Activation by exo-metallacycle Intermediates

Sahoo, S. R.; Dutta, S.; Al-Thabaiti, S. A.; Mokhtar, M.; Maiti, D.

Chem. Comm., 2021, 57, 11885

190. Transition-Metal-Catalyzed Selective Alkynylation of C-H Bonds

Anjana, S. S.; Bhowmick, S.; Carvalho, R. L.; Al-Thabaiti, S. A.; Mokhtar, M.; Júnior, E. N. S.; Maiti, D.

Adv. Synth. Catal., 2021, 363, 4994 (selected as a VIP: Very Important Publication)

189. Recent Advances in the Nitration of Olefins

Paul, N.; Maity, S.; Panja, S.; Maiti, D.

The Chemical Record, 2021, 21, 2896

188. Supported metal nanoparticles assisted catalysis: A broad concept in functionalization of ubiquitous C−H bonds

Baroliya, P.K.; Chopra. J.; Pal, T.; Maiti, S.; Al-Thabaiti, S.A.; Mokhtar, M; Maiti, D.

ChemCatChem, 2021, 13, 4655

187. Deciphering the role of silver in Pd catalyzed C-H functionalization

Bhattacharya, T.; Dutta, S.; Maiti, D.

ACS Catal., 2021, 11, 9702

186. Ligand Enabled delta-C(sp3)-H Borylation of Aliphatic Amines

H. B. Chandrashekar, Dolui. P.; Li, B.; Mandal, A.; Liu, H; Guin, S; Ge, H; Maiti, D.

Angew. Chem. Int. Ed. 2021, 60, 18194 (Appears in Hot Topic: C-H Activation)

185. Noncovalent interactions in Ir-catalyzed remote C-H borylation: A recent update

Pandit, S.; Maiti, S.; Maiti. D.

Org. Chem. Front. , 2021, 8, 4348

184. Transient directing ligands for selective metal-catalyzed C-H activation

Goswami, N.; Bhattacharya, T.; Maiti. D.

Nat. Rev. Chem. 2021, 5, 646

183. Accessing C2-Functionalized 1,3-(Benz)azoles through Transition Metal-Catalyzed C-H Activation

Basak, S.; Dutta, S.; Maiti. D.

Chem. Eur. J., 2021, 27. 10533

182. Copper mediated chemo-and stereoselective cyanation reactions

Chandra, P.; Choudhary, N.; Lahiri, G. K.; Maiti, D.; Mobin, S. M.

Asian. J. Org. Chem., 2021, 10, 198

181. Decoding directing groups and their pivotal role in C–H activation

Murali, K.; Machado, L. A.; Carvalho, R. L.; Pedrosa, L. F.; Mukherjee, R.; da Silva Junior , E. N.; Maiti. D.

Chem. Eur. J., 2021, 27, 12453

180. Transition Metal Catalyzed C-H Arylation Using Organoboron Reagents

Basak, S; Biswas, J. P.; Maiti, D.

Synthesis, 2021, 53, 315

179. Arene Diversification via Distal C(sp2)-H Functionalization

Dutta, U.; Maiti, S.; Bhattacharya, T.; Maiti, D.

Science, 2021, 372, 701

178. Effect of ligand backbone on the reactivity and mechanistic paradigm of non-heme iron(IV)-oxo during olefin epoxidation

Biswas, J. P.; Ansari, M.; Paik, A.; Sasmal, S; Paul, S; Rana, S; Rajaraman, G.; Maiti, D.

Angew. Chem. Int. Ed. 2021, 60, 14030

177. Recent Advances in External Directing Group Free C-H Functionalization of Carboxylic Acids Without Decarboxylation

Das, J.; Mal, D. K.; Maji, S.; Maiti, D.

ACS Catal. 2021, 11, 4205

176. Construction of Highly Functionalized Xanthones via Rh-Catalyzed Cascade C-H Activation/O-Annulation

Nale, S. D.; Maiti, D.; Lee Y. R.

Org. Lett 2021, 23, 2465

175. Synergistic effect of NiLDH@YZ hybrid and mechanochemical agitation on Glaser homocoupling reaction

Mokhtar, M.; Alzhrani, G.; Aazam, E. S.; Saleh, T. S.; Al-faifi, S.; Panja, S.; Maiti. D.

Chem. Eur. J., 2021, 27, 8875

174. Imine as a linchpin approach for meta-C–H functionalization

Bag, S.; Jana, S.; Pradhan, S.; Bhowmick, S.; Goswami, N.; Sinha, S. K.; Maiti, D.

Nat. Commun. 2021, 12, 1393

173. C–CN Bond Formation: An Overview of Diverse Strategies

Pimparkar, S.; Koodan, A.; Maiti, S.; Ahmed N. S.; Mostafa, M. M.; Maiti, D.

Chem. Commun. 2021, 57, 2210

172. Hexafluoroisopropanol: The Magical Solvent for Pd-Catalyzed C-H Activation

Bhattacharya, T.; Ghosh, A.; Maiti, D.

Chem. Sci., 2021, 12, 3857

171. A Catalysis Guide Focusing on C–H Activation Processes.

Carvalho, R. L.; Gleiston, G. D.; Pereira, C. L. M; Ghosh. P.; Maiti, D.; da Silva Júnior, E. N.

J. Braz. Chem. Soc. 2021, 32, 917.

170. 4′-((Diisopropylsilyl)methyl)-[1,1′-biphenyl]-2-carbonitrile

Bhattacharya, T.; Maiti, D.

Encyclopedia of Reagents for Organic Synthesis (EROS) 2021

169. 4′-Hydroxy-4,5-dimethoxy-[1,1′-biphenyl]-2-carbonitrile

Bhattacharya, T.; Maiti, D.

Encyclopedia of Reagents for Organic Synthesis (EROS) 2021

168. Recent development in transition metal-catalyzed C-H olefination

Ali, W.; Prakash, G.; Maiti, D.

Chem. Sci., 2021, 12, 2735

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Highlighted in Research Matters, Selected as Synfact of the Month Feb'24

Covered in the April issue of Synform

Org. Chem. Front. , 2021, 8, 4348

Nat. Rev. Chem. 2021, 5, 646

Chem. Eur. J., 2021, 27. 10533

Chem. Eur. J., 2021, 27, 12453

174. Imine as a linchpin approach for meta-C–H functionalization

Bag, S.; Jana, S.; Pradhan, S.; Bhowmick, S.; Goswami, N.; Sinha, S. K.; Maiti, D.

Nat. Commun. 2021, 12, 1393

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