Efficient synthesis of tetrasubstituted 2,3-allenoates and preliminary studies on bioactivities

Literature Information

Publication Date 2018-12-11
DOI 10.1039/C8QO01202D
Impact Factor 5.281
Authors

Yuan Yao, Guirong Zhu, Qin Chen, Hui Qian


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Abstract

A general and highly efficient straightforward protocol for the preparation of tetrasubstituted 2,3-allenoates through a palladium-catalyzed coupling reaction of 3-alkoxycarbonyl propargylic carbonates and boronic acids with commercially available tri(o-tolyl)phosphine as a ligand has been developed. This mild reaction exhibited a wide substrate scope and functional group compatibility, providing a highly efficient strategy to access valuable tetrasubstituted 2,3-allenoate products. Several tetrasubstituted 2,3-allenoates obtained in this study exhibited potent anti-cancer and anti-diabetic activities.

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Organic Chemistry Frontiers

Organic Chemistry Frontiers
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Organic Chemistry Frontiers publishes high-quality research from across organic chemistry. Emphases are placed on studies that make significant contributions to the field of organic chemistry by reporting either new or significantly improved protocols or methodologies. Topics include, but are not limited to the following: Organic synthesis Development of synthetic methodologies Catalysis Natural products Functional organic materials Supramolecular and macromolecular chemistry Physical and computational organic chemistry

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