Highly Enantioselective Intramolecular Morita‐Baylis‐Hillman Reaction Catalyzed by Mannose‐Based Thiourea‐phosphine

E-ISSN： 1614-7065|33|10|1111-1114

ISSN： 1001-604x

Source： CHINESE JOURNAL OF CHEMISTRY (ELECTRONIC), Vol.33, Iss.10, 2015-10, pp. : 1111-1114

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Asymmetric Construction of Highly Functionalized Spirobarbiturate‐Cyclopentenes through Chiral Phosphine‐Catalyzed [3+2] Annulation of Morita–Baylis–Hillman Carbonates with Barbiturate‐Derived Alkenes

ADVANCED SYNTHESIS & CATALYSIS, Vol. 358, Iss. 18, 2016-09 ,pp. : 2867-2872

John Wiley & Sons Inc

Access to resources Recommend Favorite

Tunable Bifunctional Phosphine–Squaramide Promoted Morita–Baylis–Hillman Reaction of N‐Alkyl Isatins with Acrylates

ADVANCED SYNTHESIS & CATALYSIS, Vol. 357, Iss. 9, 2015-06 ,pp. : 2132-2142

John Wiley & Sons Inc

Access to resources Recommend Favorite

Morita–Baylis–Hillman Reactions with Nitroalkenes: A Case Study

EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, Vol. 2015, Iss. 17, 2015-06 ,pp. : 3679-3688

John Wiley & Sons Inc

Access to resources Recommend Favorite

Synthesis of 3,4,5‐Trisubstituted Isoxazoles from Morita–Baylis–Hillman Acetates by an NaNO2/I2‐Mediated Domino Reaction

ANGEWANDTE CHEMIE, Vol. 127, Iss. 37, 2015-09 ,pp. : 11076-11080

John Wiley & Sons Inc

Access to resources Recommend Favorite

Synthesis of 3,4,5‐Trisubstituted Isoxazoles from Morita–Baylis–Hillman Acetates by an NaNO2/I2‐Mediated Domino Reaction

ANGEWANDTE CHEMIE INTERNATIONAL EDITION, Vol. 54, Iss. 37, 2015-09 ,pp. : 10926-10930

John Wiley & Sons Inc

Access to resources Recommend Favorite