Palladium-catalyzed regio- and stereoselective access to allyl ureas/carbamates: facile synthesis of imidazolidinones and oxazepinones-Reference-Cited by-同舟云学术

Palladium-catalyzed regio- and stereoselective access to allyl ureas/carbamates: facile synthesis of imidazolidinones and oxazepinones

Published:2020 Issue:33 Volume:18 Page:6564-6570
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Taily Irshad Maajid¹²³⁴,Saha Debarshi¹²³⁴,Banerjee Prabal¹²³⁴^ORCID

Affiliation:

1. Department of Chemistry

2. Indian Institute of Technology Ropar

3. Rupnagar

4. India

Abstract

Highly regio- and stereoselective decarboxylative amidation of VECs to allyl ureas/carbamates is investigated. The allyl derivatives were further transformed to imidazolidinones and oxazepinones under mild reaction conditions.

Funder

Department of Science and Technology, Ministry of Science and Technology, India

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/2020/OB/D0OB01514H

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2. Transition Metal-Catalyzed Regio- and Stereoselective Aminobromination of Olefins with TsNH2 and NBS as Nitrogen and Bromine Sources

3. Metal and carbene organocatalytic relay activation of alkynes for stereoselective reactions

4. Regio- and stereoselective carbon-carbon bond formation through transition metal catalysis. The influence of catalyst chirality on selective ethylmagnesiation of chiral, nonracemic alcohols and ethers

5. Old but Gold: Tracking the New Guise of Histone Deacetylase 6 (HDAC6) Enzyme as a Biomarker and Therapeutic Target in Rare Diseases

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