Phosphine-Catalyzed Enantioselective [4 + 2] Cycloaddition–Semipinacol-Type-Rearrangement Reaction of Morita–Baylis–Hillman Carbonates

Yuan Zhong (205199)
Xiaoyun Zhao (5463836)
Lu Gan (33435)
Sihua Hong (5463833)
Xianxing Jiang (1555024)

Publication date

June 2018

DOI

10.1021/acs.orglett.8b01661.s001

Abstract

The chiral phosphine-triggered electrophilic ylide intermediate for a Morita–Baylis–Hillman carbonates activation strategy provides a promising method for the design of organocatalytic intermolecular higher-order annulation processes

Extracted data

We use cookies to provide a better user experience.

Data Protection

Phosphine-Catalyzed Enantioselective [4 + 2] Cycloaddition–Semipinacol-Type-Rearrangement Reaction of Morita–Baylis–Hillman Carbonates

Abstract

Extracted data

Phosphine-Catalyzed Enantioselective [4 + 2] Cycloaddition–Semipinacol-Type-Rearrangement Reaction of Morita–Baylis–Hillman Carbonates

Abstract

Extracted data

Related items

Related items