Magnesium catalyzed [3 + 3] heteroannulation of α-enolic dithioesters with MBH acetate: access to functionalized 3,4-dihydro-2<i>H</i>-thiopyrans-Reference-Cited by-同舟云学术

Magnesium catalyzed [3 + 3] heteroannulation of α-enolic dithioesters with MBH acetate: access to functionalized 3,4-dihydro-2H-thiopyrans

Published:2022 Issue:34 Volume:20 Page:6784-6798
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Soni Sonam¹,Shukla Gaurav¹,Singh Maya Shankar¹^ORCID

Affiliation:

1. Department of Chemistry, Institute of Science, Banaras Hindu University, Varanasi 221005, India

Abstract

An efficient heteroannulation employing racemic Morita–Baylis–Hillman acetate and α-enolic dithioesters enabling the formation of dihydro-2H-thiopyrans is reported.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2022/OB/D2OB01258H

Reference72 articles.

1. Magnesium Catalysis in Asymmetric Synthesis

2. Organocatalytic Enantioselective Amination of Morita-Baylis-Hillman Carbonates with Masked Ammonia: A Facile Method for the Synthesis of Unprotected α-Methylene-β-Amino Esters

3. Magnesium-catalyzed stereoselective transformations – A survey through recent achievements

4. Magnesium Catalysis in Asymmetric Synthesis

5. The synthesis of 2,3-disubstituted cyclopentenones using the ramberg-bäcklund reaction in conjunction with organocopper chemistry

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