Serendipitous synthesis of cross-conjugated dienes by cascade deconstructive esterification of thiomorpholinone-tethered alkenoic acids-Reference-Cited by-同舟云学术

Serendipitous synthesis of cross-conjugated dienes by cascade deconstructive esterification of thiomorpholinone-tethered alkenoic acids

Published:2023 Issue:5 Volume:13 Page:3181-3185
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Farah Abdikani Omar¹,Garcia Jorge¹,Borg Claire¹,Beng Timothy K.¹^ORCID

Affiliation:

1. Department of Chemistry, Central Washington University, Ellensburg, WA 98926, USA

Abstract

Versatile amino-1,3-dienes have been prepared in a stereocontrolled manner, by engaging thiomorpholinone-tethered alkenoic acids in a cascade process featuring base-mediated esterification, C–S bond cleavage, and concomitant 1,2-styryl migration.

Funder

Central Washington University

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2023/RA/D2RA07916J

Reference69 articles.

1. Butadiene production process overview

2. Copper-Mediated Coupling Reactions and Their Applications in Natural Products and Designed Biomolecules Synthesis

3. Palladium-Catalyzed 1,4-Difunctionalization of Butadiene To Form Skipped Polyenes

4. Regioselective Hydroacylation of 1,3-Dienes by Cobalt Catalysis

5. Catalytic Diamination of Olefins via N–N Bond Activation

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