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Debayan Roy - Publications

Affiliations: 
2016- IIT Madras 
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7 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2023 Baire B, Gandhi S, Bommanaboina B, Roy D. The Bis(indolylmethyl) ethers: Design, Prototypical Synthesis, and Scope Studies. The Journal of Organic Chemistry. 88: 12115-12120. PMID 37537963 DOI: 10.1021/acs.joc.3c01116  0.662
2023 Roy D, Baire B. Diastereoselective Biomimetic Synthesis of Dimeric Tetrahydrocarbazoles via a Copper(II)-Catalyzed Cycloisomerization-[3+2] Cyclodimerization Cascade. Angewandte Chemie (International Ed. in English). e202304557. PMID 37134297 DOI: 10.1002/anie.202304557  0.653
2022 Roy D, Tharra P, Baire B. An approach to functionalized carbazoles from -enoate propargylic alcohols. A unified total synthesis of -Me-carazostatin, -Me-carbazoquinocin C and -Me-lipocarbazole A4. Chemical Communications (Cambridge, England). 58: 10210-10213. PMID 36000534 DOI: 10.1039/d2cc03526j  0.694
2021 Roy D, Tharra P, Baire B. An Approach for the Generation of γ-Propenylidene-γ-butenolides and Application to the Total Synthesis of Rubrolides. Organic Letters. PMID 34259007 DOI: 10.1021/acs.orglett.1c01529  0.712
2021 Roy D, Tharra P, Baire B. An Approach for the Generation of γ-Propenylidene-γ-butenolides and Application to the Total Synthesis of Rubrolides. Organic Letters. PMID 34259007 DOI: 10.1021/acs.orglett.1c01529  0.712
2020 Baire B, Roy D. Evidence for atropisomerism in polycyclic γ-butenolides. Synthesis, scope and spectroscopic studies. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 33378093 DOI: 10.1002/chem.202005174  0.699
2018 Roy D, Tharra P, Baire B. Intercepted Meyer-Schuster Rearrangements in Organic Synthesis Asian Journal of Organic Chemistry. 7: 1015-1032. DOI: 10.1002/AJOC.201800089  0.672
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