Domino reaction of cyclic sulfamidate imines with Morita–Baylis–Hillman acetates promoted by DABCO: a metal-free approach to functionalized nicotinic acid derivatives-Reference-Cited by-同舟云学术

Domino reaction of cyclic sulfamidate imines with Morita–Baylis–Hillman acetates promoted by DABCO: a metal-free approach to functionalized nicotinic acid derivatives

Published:2017 Issue:15 Volume:15 Page:3286-3297
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Majee Debashis¹²³⁴,Biswas Soumen¹²³⁴,Mobin Shaikh M.¹²³⁴^ORCID,Samanta Sampak¹²³⁴^ORCID

Affiliation:

1. Discipline of Chemistry

2. Indian Institute of Technology Indore

3. Simrol

4. India

Abstract

A series of 4,6-diarylnicotinates have been prepared in good to excellent yields via a domino reaction of cyclic sulfamidate imines with MBH acetates in 2-MeTHF promoted by DABCO under an O₂ atmosphere.

Funder

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/2017/OB/C7OB00240H

Reference56 articles.

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