Efficient asymmetric syntheses of α-quaternary lactones and esters through chiral bifunctional sulfide-catalyzed desymmetrizing bromolactonization of α,α-diallyl carboxylic acids-Reference-Cited by-同舟云学术

Efficient asymmetric syntheses of α-quaternary lactones and esters through chiral bifunctional sulfide-catalyzed desymmetrizing bromolactonization of α,α-diallyl carboxylic acids

Published:2021 Issue:83 Volume:57 Page:10907-10910
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Hiraki Mana¹,Okuno Ken¹,Nishiyori Ryuichi¹,Noser Ahmed A.¹²^ORCID,Shirakawa Seiji¹^ORCID

Affiliation:

1. Department of Environmental Science, Graduate School of Fisheries and Environmental Sciences, Nagasaki University, 1-14 Bunkyo-machi, Nagasaki 852-8521, Japan

2. Department of Chemistry, Faculty of Science, Tanta University, Tanta 31527, Egypt

Abstract

Efficient asymmetric syntheses of α-quaternary lactones and esters were achieved via the chiral bifunctional sulfide-catalyzed desymmetrizing bromolactonization of α,α-diallyl carboxylic acids.

Funder

Takahashi Industrial and Economic Research Foundation

Japan Society for the Promotion of Science

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2021/CC/D1CC03874E

Reference87 articles.

1. Enantioselective Halocyclization Reactions for the Synthesis of Chiral Cyclic Compounds

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4. New Catalytic Approaches towards the Enantioselective Halogenation of Alkenes

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