Design and development of intramolecular doubly vinylogous Michael addition to access 3-aryl substituted 2-alkenyl-benzofurans and -indoles-Reference-Cited by-同舟云学术

Design and development of intramolecular doubly vinylogous Michael addition to access 3-aryl substituted 2-alkenyl-benzofurans and -indoles

Published:2023 Issue: Volume: Page:
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Subbi Reddy Manyam¹²,Nanubolu Jagadeesh Babu³^ORCID,Suresh Surisetti¹²^ORCID

Affiliation:

1. Department of Organic Synthesis and Process Chemistry, CSIR-Indian Institute of Chemical Technology (CSIR-IICT), Hyderabad 500 007, India

2. Academy of Scientific and Innovative Research (AcSIR), Ghaziabad 201002, India

3. Laboratory of X-Ray Crystallography, Department of Analytical Chemistry, CSIR-Indian Institute of Chemical Technology (CSIR-IICT), Hyderabad 500 007, India

Abstract

The first intramolecular doubly vinylogous Michael addition (DVMA) has been revealed for the construction of 2-alkenyl benzofuran and 2-alkenyl indole derivatives.

Funder

Indian Council of Medical Research

Science and Engineering Research Board

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2023/OB/D3OB00861D

Reference37 articles.

1. Enantioselective Vinylogous Organocascade Reactions

2. New Developments of the Principle of Vinylogy as Applied to π-Extended Enolate-Type Donor Systems