
167. Removal and modification of directing groups used in metal-catalyzed C–H functionalization: The magical step of conversion into ‘conventional’ functional groups
Carvalho. R. L.; Almeida, R. G.; Karunanidhi. M.; Machado, L. A.; Pedrosa. L. F.; Dolui. P.; Maiti. D.; Da Silva Jr. E. N.
Org. Biomol. Chem. 2020, 19, 525


166. Organopalladium Intermediates in Coordination Directed C(sp3) -H Functionalizations
S. S. Anjana.; Dutta, A.; Lahiri. G. K.; Maiti, D.


165. Transition Metal Catalyzed Enantioselective C(sp2)–H Bond Functionalization
Achar, T; Maiti, S.; Jana, S.; Maiti, D.


164. Evolution of Strept(avidin) based artificial metalloenzymes in organometallic catalysis
Mukherjee, P.; Maiti, D.


163. Transition Metal Catalyzed C-H Allylation Reactions
Dutta, S.; Bhattacharya, T.; Werz, D. B.; Maiti, D.


162. Organic synthesis with the most abundant transition metal- Iron: From rust to multitasking catalysts
Rana, S.; Biswas, J. P.; Paul, S.; Paik, A.; Maiti, D.
Chem. Soc. Rev., 2020, 50, 243


161. Diverse Strategies for Transition Metal Catalyzed Distal C(sp3)-H Functionalizations
Das, J.; Guin, S.; Maiti, D.


A special interview of Prof. Maiti on the eve of 10th anniversary of the Chemical Science journal

160. Transition Metals and Transition Metals/Lewis Acid Cooperative Catalysis for Directing Group Assisted para- C−H Functionalization
Sasmal, S.; Dutta, U.; Lahiri, G. K.; Maiti, D.


159. A Direct Route to Six and Seven Membered Lactones via γ-C(sp3)-H Activation: A Simple Protocol to Build Molecular Complexity
Das, J†.; Dolui, P†.; Ali, W.; Biswas, J. P.; Chandrashekar, H. B.; Prakash, G; Maiti, D.
(† = Authors contributed equally)


158. Fe-catalyzed aziridination is governed by the electron affinity of the active imido-iron species
Coin, G; Patra, R.; Rana, S; Biswas, J.P.; Dubourdeaux, P; Clémancey, M.; de Visser, S. P.; Maiti, D.; Maldivi, P.; Latour, J-M.


157. Para-Selective Arylation of Arenes: A Direct Route to Biaryls by Norbornene Relay Palladation
Dutta, U†.; Porey, S†.; Pimparkar, S.; Mandal, A; Grover, J; Koodan, A; Maiti, D.
Angew. Chem. Int. Ed. 2020, 59, 20831
(† = Authors contributed equally)


156. Phenol, 2-(5-pyrimidinyl)
Guin, S.; Maiti. D.
Encyclopedia of Reagents for Organic Synthesis (EROS) 2020

155. 2-Hydroxy-4-methoxybenzonitrile
Guin, S.; Maiti. D.
Encyclopedia of Reagents for Organic Synthesis (EROS) 2020

154. Phenol, 2-(8-nitro-3-quinolinyl)
Dutta, U.; Maiti. D.
Encyclopedia of Reagents for Organic Synthesis (EROS) 2020

153. 1,1'-Biphenyl]-2-carbonitrile, 4'-hydroxy-4,5-dimethoxy
Bhattacharya, T.; Maiti. D.
Encyclopedia of Reagents for Organic Synthesis (EROS) 2020

152. Redox-active ligand incorporated coordination complexes and their catalytic implications
Maiti. D.; Mondal, B.; Ghosh, P.
Inorg. Chim. Act., 2020, 509, 119635

151. Special issue celebrating 60th birthday of Prof. G.K Lahiri
Maiti. D.; Mondal, B.; Ghosh, P.
Coordination Chemistry Reviews, 2020, 414, 213268

150. Introduction in "Remote C-H Bond Functionalizations: Methods and Strategies in Organic Synthesis"
Edited by Prof. D. Maiti and Dr. S. Guin,
Dutta, U.; Guin, S.; Maiti. D. Wiley-VCH, 2020

149. Transition Metal Catalyzed Distal para-Selective C-H Functionalization in “Remote C-H Bond Functionalizations: Methods and Strategies in Organic Synthesis”
Edited by Prof. D. Maiti and Dr. S. Guin.
Dutta, U.; Maiti. D. Wiley-VCH, 2020


148. Copper in Efficient Synthesis of Aromatic Heterocycleswith Single Heteroatom
Pal, T.; Lahiri, G. K.; Maiti. D.
Eur. J. Org. Chem., 2020, 6859


147. Transition Metal Promoted Cascade Heterocycles Synthesis via C–H Functionalization
Baccalini, A.; Faita, G.; Zanoni, G.; Maiti. D.

Bag, S.; K, S.; Mondal, A.; Jayarajan, R.; Dutta, U.; Porey, S.; Sunoj, R. B.; Maiti. D.
J. Am. Chem. Soc, 2020, 142, 12453


145. Overriding Ortho Selectivity by Template Assisted Meta-C–H Activation of Benzophenone
Casali, E.; Kalra, P.; Brochetta, M.; Borsari, T.; Gandini, A.; Patra, T.; Zanoni, G.; Maiti, D.


144. A directing group assisted ruthenium catalyzed approach to access meta-nitrated phenol
Sasmal, S.; Sinha, S. K.; Lahiri, G. K.; Maiti, D.


143. Diverse meta-C–H Functionalization of Amides
Gholap, A†.; Bag, S†.; Pradhan, S.; Kapdi, A. R.; Maiti, D.
(† = Authors contributed equally)
ACS Catalysis 2020, 10, 5347 (ASAP)


142. Ultrasound-facilitated direct meta-C-H functionalization of arene: A time economical strategy under ambient temperature with improved yield and selectivity
Jayarajan, R.; Chandrashekar, H. B.; Dalvi, A. K.; Maiti, D.



141. An update on distal C(sp3)−H functionalization involving 1,5-HAT emerging from nitrogen radicals
Goswami, N.; Maiti. D.
Israel. J. Chem., 2020, 60, 303

140. Para-Selective Cyanation of Arenes by H-bonded Template
Pimparkar, S.; Bhattacharya, T.; Maji, A.; Saha, A.; Jayarajan, R.; Dutta, U.; Lu, G.; Lupton, D. W.; Maiti, D.


139. Highvalent 3d Metal-Oxo Mediated C-H Halogenation: Biomimetic Approaches.
Biswas, J. P.; Guin, S.; Maiti. D.
Coordination Chemistry Reviews, 2020, 408, 213174

Porey, S.; Zhang, X.; Bhowmick, S.; Singh, V. K.; Guin, S.; Paton, R. S.; Maiti. D.
J. Am. Chem. Soc, 2020, 142, 3762 (selected in "JACS Early Career Investigators" virtual issue)


137. Recent Advances in Cobalt-Catalysed C–H Functionalizations
Baccalini, A.; Vergura, S.; Dolui, P.; Zanoni, G.; Maiti. D
Org. Biomol. Chem. 2019, 17, 10119

136. Cobalt-Catalyzed C(sp2)–H Allylation of Biphenyl Amines with Unbiased Terminal Olefins
Baccalini, A.; Vergura, S.; Dolui, P.; Maiti, S.; Dutta, S.; Maity, S.; Khan, F. F.; Lahiri, G. K.; Zanoni, G.; Maiti. D.


135. Orthogonal Selectivity in C-H Olefination: Synthesis of Branched Vinylarene with Unactivated Aliphatic Substitution
Agasti, S.; Mondal, B.; Achar, T. K.; Sinha, S. K.; S. S. Anjana.; Szabo, K. J.; Schoenebeck, F.; Maiti, D.


134. Access to Multifunctionalized Benzofurans by Aryl Nickelation of Alkynes: Efficient Synthesis of the Anti-Arrhythmic Drug Amiodarone
Iqbal, N.; Iqbal, N.; Maiti, D.; Cho, E. J.
Angew. Chem. Int. Ed. 2019, 131,15955


133. Ligand-Enabled Pd(II)-Catalyzed Iterative γ-C(sp3)-H Arylation of Free Aliphatic Acid
Dolui, P†.; Das, J†.; Chandrashekar, H. B.; Anjana, S. S.; Maiti, D.
(† = Authors contributed equally)
Angew. Chem. Int. Ed. 2019, 58,13773 (HOT PAPER)


132. Co‐ordination assisted distal C−H alkylation of fused heterocycles
Kankanala, R†.; Biswas, J. P†.; Jana, S.; Achar, T. K.; Porey, S.; Maiti, D.
(† = Authors contributed equally)
Angew. Chem. Int. Ed. 2019, 131,13946


131. Direct meta-C-H Perfluoroalkenylation of Arenes Enabled by a Cleavable Pyrimidine-Based Template
Brochetta, M.; Borsari, T.; Bag, S.; Jana, S.; Maiti, S.; Porta, A.; Werz, D.; Zanoni, G.; Maiti, D.


130. Rhodium Catalyzed Template-Assisted Distal para-C-H Olefination
Dutta, U.; Maiti, S.; Pimparkar, S.; Maiti, S.; Gahan, L. R.; Krenske, E. H.; Lupton, D. W.; Maiti, D.
Chem. Sci. 2019, 10, 7426


129. Regioselective Synthesis of Fused Furans by Decarboxylative Annulation of α,β-Alkenyl Carboxylic Acid with Cyclic Ketone: Synthesis of Di-Heteroaryl Derivatives
Agasti, S.; Pal, T.; Achar, T. K.; Maiti, S.; Pal, D.; Mandal, S.; Daud, K.; Lahiri, G. K.; Maiti, D.
Angew. Chem. Int. Ed. 2019, 58, 11039 (VIP Paper)


128. Palladium-Catalyzed Directed meta-Selective C-H Allylation of Arenes: Unactivated Internal Olefins as Allyl Surrogates
Achar, T. K.; Zhang, X.; Mondal, R.; Shanavas, M. S.; Maiti, S.; Maity, S.; Pal, N.; Paton, R. S.; Maiti, D.
Angew. Chem. Int. Ed. 2019,58,10353


127. Palladium catalyzed template directed C-5 selective olefination of thiazoles
Achar, T. K.; Biswas, J.; Porey, S.; Pal, T.; Ramakrishna, K.; Maiti, S.; Maiti, D.


126. Photocatalyzed Borylation Using Water-Soluble Quantum Dots
Chandrasekhar, H. B.; Maji, A.; Halder, G.; Banerjee, S.; Bhattacharyya, S.; Maiti, D.


125. Palladium‐Catalyzed Selective meta‐C−H Deuteration of Arenes: Reaction Design and Applications
Bag, S.; Petzold, M.; Sur, A.; Bhowmick, S.; Werz, D.; Maiti, D.
Chem. Eur. J 2019, 25,9433 (HOT Paper)


124. Bismuth Nitrate as a Source of Nitro Radical in Ipso-Nitration of Carboxylic Acids
Agasti, S.; Maiti, S.; Maity, S.; Anniyappan, M.; Talawar, M. B.; Maiti, D.

123. Iterative Arylation of Amino Acids and Aliphatic Amines via-C(sp3)-H Activation: Experimental and Computational Exploration
Guin, S†.; Dolui, P†.; Zhang, X.; Paul, S.; Singh, V. K; Pradhan, S.; Chandrashekar, H. B.; S. S. Anjana.; Paton, R. S.; Maiti, D.
(† = Authors contributed equally)
Angew. Chem. Int. Ed. 2019, 58, 5633-5638


122. Fabrication of an amyloid fibril-palladium nanocomposite: A sustainable catalyst for C-H activation and the electrooxidation of ethanol
Jayarajan, R.; Kumar, R.; Gupta, J.; Dev, G.; Kadu, P.; Chatterjee, D.; Bahadur, D.; Maiti, D.; Maji, S. K.
J. Mater. Chem. A, 2019, 7, 4486


121. Game of Directors: Accessing Remote Meta- and Para-C-H Bonds With Covalently Attached Directing Groups
Dey, A.; Sinha, S. K.; Achar, T. K.; Maiti, D.
Angew. Chem.Int. Ed 2019, 58, 10820


120. Palladium Catalyzed Regioselective C4-Arylation and Olefination of Indoles and Azaindoles
Thrimurtulu, N.; Dey, A.; Singh, A.; Pal, K.; Maiti, D.; Volla, C. M. R.
Adv. Synth. Catal. 2018, 365, 1441


119.Trifluoromethylation of Allenes: An Expedient Access to α-Trifluoromethylated Enones at Room Temperature
Brochetta, M.; Borasari, T.; Gandini, A.; Porey, S.; Deb, A.; Casali, E.; Chakraborty, A.; Zanoni, G.; Maiti, D.
Chem. Eur. J 2018, 25, 750


118. Role of hexafluoroisopropanol in C‒H activation
Sinha, S. K.; Bhattacharya, T.; Maiti, D.
React. Chem. Eng., 2018 , 4, 1492
117.Regiocontrolled Remote C-H Olefination of Small Heterocycles
Achar, T. K.; Ramakrishna, K.; Pal, T.; Porey, S.; Dolui, P.; Biswas, J. P.; Maiti, D.
Chem. Eur. J. 2018 , 24, 17906




116.Mechanistic Insights on Orthogonal Selectivity in Heterocycle Synthesis
MaJi, A.; Yernaidu, R.; Sunoj, R. B.; Maiti, D.
ACS Catal. 2018, 8, 10111−10118

115. Template assisted para-C‒H activation Template assisted para C‒H activation
Sinha, S.K.; Sasmal, S; Lahiri, G. K.; Maiti, D.
J. Indian. Chem. Soc 2018, 9, 7843

114. Selective C-H Halogenation over Hydroxylation by Non-heme Iron(IV)-oxo
Rana, S.; Biswas, J. P; Sen, A.; Clemency, M.; Blondin, G.; Latour, J-M.; Rajaraman, G.; Maiti, D.
Chem. Sci. 2018, 9, 7843