Lithium-Promoted Cycloaddition of Indole-2,3-dienolates and Carbon Disulfide as a One-Pot Route to Thiopyrano[4,3-b]indole-3(5H)-thiones-Reference-Cited by-同舟云学术

Lithium-Promoted Cycloaddition of Indole-2,3-dienolates and Carbon Disulfide as a One-Pot Route to Thiopyrano[4,3-b]indole-3(5H)-thiones

Published:2021-08-02 Issue:17 Volume:86 Page:11698-11707
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Suzdalev Konstantin F.¹^ORCID,Vyalyh Julia V.¹^ORCID,Tkachev Valery V.²,Lysenko Ekaterina A.¹,Burov Oleg N.¹,Lisovin Anton V.¹,Kletskii Mikhail E.¹,Kurbatov Sergey V.¹

Affiliation:

1. Department of Chemistry, Southern Federal University, Rostov-on-Don 344090, Russia

2. Institute of Problems of Chemical Physics, Russian Academy of Sciences, Chernogolovka 142432, Russia

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.1c01200

Reference51 articles.

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2. Generation ofN-(tert-Butoxycarbonyl)indole-2,3-quinodimethane and Its [4+2]-Type Cycloaddition

3. Synthesis of new biologically active isothiazolo[4,5-b]carbazole-type tetracyclic derivatives via an indole-2,3-quinodimethane approach

4. Asymmetric Diels–Alder Reaction of 2-Methyl-3-indolylmethanols via in Situ Generation of o-Quinodimethanes

5. Multicatalytic Asymmetric Synthesis of Complex Tetrahydrocarbazoles via a Diels–Alder/Benzoin Reaction Sequence

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