Year |
Citation |
Score |
2023 |
Pramanik S, Mondal PP, Maity S. Organo-photoredox-Catalyzed Selective Mono- and Bis-C-H Alkylation of Electron-Rich (Hetero)Arenes. The Journal of Organic Chemistry. PMID 37823605 DOI: 10.1021/acs.joc.3c01757 |
0.67 |
|
2023 |
Mondal S, Chatterjee N, Maity S. Recent Developments on Photochemical Synthesis of 1,n-Dicarbonyls. Chemistry (Weinheim An Der Bergstrasse, Germany). e202301147. PMID 37335758 DOI: 10.1002/chem.202301147 |
0.376 |
|
2023 |
Singh D, Pramanik S, Maity S. Photocatalytic sequential C-H functionalization expediting acetoxymalonylation of imidazo heterocycles. Beilstein Journal of Organic Chemistry. 19: 666-673. PMID 37205129 DOI: 10.3762/bjoc.19.48 |
0.677 |
|
2022 |
Samanta A, Pramanik S, Mondal S, Maity S. Zinc acetate-promoted blocking of the ATRA process with alkyl halides enabling photochemical alkylamination of olefins. Chemical Communications (Cambridge, England). 58: 8400-8403. PMID 35796040 DOI: 10.1039/d2cc02574d |
0.738 |
|
2020 |
Roy Chowdhury S, Singh D, Hoque IU, Maity S. Organic Dye-Catalyzed Intermolecular Radical Coupling of α-Bromocarbonyls with Olefins: Photocatalytic Synthesis of 1,4-Ketocarbonyls Using Air as an Oxidant. The Journal of Organic Chemistry. PMID 33054198 DOI: 10.1021/acs.joc.0c01985 |
0.491 |
|
2019 |
Hoque IU, Roy Chowdhury S, Maity S. Photoredox-Catalyzed Intermolecular Radical Arylthiocyanation/Arylselenocyanation of Alkenes: Access to Aryl-Substituted Alkylthiocyanates/ Alkylselenocyanates. The Journal of Organic Chemistry. PMID 30665295 DOI: 10.1021/acs.joc.8b03155 |
0.715 |
|
2018 |
Maity S, Roy Chowdhury S, Hoque IU. TBAI/TBHP-Promoted Generation of Malonyl Radicals: Oxidative Coupling with Styrenes Leads to γ-Keto Diesters. Chemistry, An Asian Journal. PMID 30039927 DOI: 10.1002/asia.201800992 |
0.717 |
|
2018 |
Maity S, Sar S, Ghorai P. Primary Aminothiourea-Catalyzed Enantioselective Synthesis of Rauhut-Currier Adducts of 3-Arylcyclohexenone with a Tethered Enone on the Aryl Moiety at the Ortho-Position. Organic Letters. PMID 29558154 DOI: 10.1021/acs.orglett.7b03959 |
0.336 |
|
2017 |
Thrimurtulu N, Khan S, Maity S, Volla CMR, Maiti D. Palladium catalyzed direct aliphatic γC(sp(3))-H alkenylation with alkenes and alkenyl iodides. Chemical Communications (Cambridge, England). PMID 29104971 DOI: 10.1039/C7Cc05703B |
0.313 |
|
2017 |
Maity S, Saha M, Hazra G, Ghorai P. Switchable Chemoselectivity for Organocatalytic, Asymmetric Malononitrile Addition to ortho-Formyl Chalcones. Organic Letters. PMID 29064718 DOI: 10.1021/acs.orglett.7b02862 |
0.325 |
|
2017 |
Maity S, Dolui P, Kancherla R, Maiti D. Introducing unactivated acyclic internal aliphatic olefins into a cobalt catalyzed allylic selective dehydrogenative Heck reaction. Chemical Science. 8: 5181-5185. PMID 28970904 DOI: 10.1039/C7Sc01204G |
0.308 |
|
2017 |
Hazra G, Maity S, Bhowmick S, Ghorai P. Organocatalytic, enantioselective synthesis of benzoxaboroles via Wittig/oxa-Michael reaction Cascade of α-formyl boronic acids. Chemical Science. 8: 3026-3030. PMID 28451370 DOI: 10.1039/c6sc04522g |
0.323 |
|
2017 |
Mallampudi NA, Reddy GS, Maity S, Mohapatra DK. Gold(I)-Catalyzed Cyclization for the Synthesis of 8-Hydroxy-3- substituted Isocoumarins: Total Synthesis of Exserolide F. Organic Letters. PMID 28383900 DOI: 10.1021/Acs.Orglett.7B00673 |
0.319 |
|
2017 |
Das D, Poddar P, Maity S, Samanta R. Rhodium(III)-Catalyzed C6-Selective Arylation of 2-Pyridones and Related Heterocycles Using Quinone Diazides: Syntheses of Hetero-Arylated Phenols. The Journal of Organic Chemistry. PMID 28277659 DOI: 10.1021/Acs.Joc.7B00135 |
0.354 |
|
2014 |
Nguyen TH, Maity S, Zheng N. Visible light mediated intermolecular [3 + 2] annulation of cyclopropylanilines with alkynes. Beilstein Journal of Organic Chemistry. 10: 975-80. PMID 24991247 DOI: 10.3762/Bjoc.10.96 |
0.5 |
|
2012 |
Maity S, Zheng N. A visible-light-mediated oxidative C-N bond formation/aromatization cascade: photocatalytic preparation of N-arylindoles. Angewandte Chemie (International Ed. in English). 51: 9562-6. PMID 22915489 DOI: 10.1002/Anie.201205137 |
0.635 |
|
2012 |
Maity S, Zhu M, Shinabery RS, Zheng N. Intermolecular [3+2] cycloaddition of cyclopropylamines with olefins by visible-light photocatalysis. Angewandte Chemie (International Ed. in English). 51: 222-6. PMID 22109785 DOI: 10.1002/Anie.201106162 |
0.517 |
|
2010 |
Maity S, Matcha K, Ghosh S. Synthetic studies on schisandra nortriterpenoids. Stereocontrolled synthesis of enantiopure C-5-epi ABC ring systems of micrandilactone A and lancifodilactone G using RCM. The Journal of Organic Chemistry. 75: 4192-200. PMID 20491457 DOI: 10.1021/Jo1006448 |
0.566 |
|
2010 |
Matcha K, Maity S, Malik CK, Ghosh S. Expedient route to CDE ring system of schintrilactones through tandem ROM–RCM of a norbornene derivative Tetrahedron Letters. 51: 2754-2757. DOI: 10.1016/J.Tetlet.2010.03.074 |
0.521 |
|
2010 |
Ghosh S, Hossain MF, Malik CK, Maity S. Effect of ring fusion stereochemistry on double bond geometry. Unexpected formation of nine-membered cyclic ether with E-configurated double bond through RCM Tetrahedron. 66: 9159-9164. DOI: 10.1016/J.Tet.2010.09.084 |
0.463 |
|
2010 |
Maity S, Ghosh S. An asymmetric route to 2,3-epoxy-syn-1,4-cyclohexane diol derivatives using ring closing metathesis (RCM) Journal of Chemical Sciences. 122: 791-800. DOI: 10.1007/S12039-010-0066-Z |
0.577 |
|
2009 |
Ghosh M, Bose S, Maity S, Ghosh S. Enantiodivergent synthesis of (−)-methylenolactocin and (+)-methylenolactocin from d-mannitol Tetrahedron Letters. 50: 7102-7104. DOI: 10.1016/J.Tetlet.2009.10.011 |
0.523 |
|
2009 |
Maity S, Ghosh S. A direct route to angularly substituted hydrindanes. Formal synthesis of bakkenolide-A and synthesis of an advanced intermediate to umbellactal Tetrahedron. 65: 9202-9210. DOI: 10.1016/J.Endend.2010.01.013 |
0.543 |
|
2008 |
Maity S, Ghosh S. Rapid assembly of the functionalized tricyclic core of umbellactal through domino metathesis involving ROM-RCM of a norbornene derivative Tetrahedron Letters. 49: 1133-1136. DOI: 10.1016/J.Tetlet.2007.12.064 |
0.51 |
|
2007 |
Maity S, Ghosh S. The first total synthesis of sequosempervirin A through an orthoester Claisen rearrangement—ring closing metathesis sequence Tetrahedron Letters. 48: 3355-3358. DOI: 10.1016/J.Tetlet.2007.03.084 |
0.479 |
|
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