Diastereoselective synthesis of <i>trans</i>-2,3-dihydroindoles <i>via</i> formal [4 + 1] annulation reactions of a sulfonium ylide-Reference-Cited by-同舟云学术

Diastereoselective synthesis of trans-2,3-dihydroindoles via formal [4 + 1] annulation reactions of a sulfonium ylide

Published:2024 Issue:3 Volume:22 Page:621-632
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Jain Anshul¹^ORCID,Kumari Akanksha¹^ORCID,Metre Ramesh K.¹^ORCID,Rana Nirmal K.¹^ORCID

Affiliation:

1. Department of Chemistry, Indian Institute of Technology Jodhpur, Jodhpur-342030, India

Abstract

We have established an in situ generated sulfonium-ylide mediated annulation to construct 2,3-disubstituted-2,3-dihydroindoles and extended to construct dihydrobenzofurans.

Funder

Science and Engineering Research Board

Council of Scientific and Industrial Research, India

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2024/OB/D3OB01793A

Reference36 articles.

1. Formal [4+1] Annulation Reactions in the Synthesis of Carbocyclic and Heterocyclic Systems

2. Isocyanide based [4+1] cycloaddition reactions: an indispensable tool in multi-component reactions (MCRs)

3. Ylide formal [4 + 1] annulation

4. Synthesis of Heterocycles by Formal Cycloadditions of Isocyanides

5. Recent Advances in the Chemistry of Conjugated Nitrosoalkenes and Azoalkenes

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