Stereoselective Organocatalytic Synthesis of Oxindoles with Adjacent Tetrasubstituted Stereocenters

E-ISSN： 1521-3757|127|28|8311-8315

ISSN： 0044-8249

Source： ANGEWANDTE CHEMIE, Vol.127, Iss.28, 2015-07, pp. : 8311-8315

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

Stereoselective Organocatalytic Synthesis of Oxindoles with Adjacent Tetrasubstituted Stereocenters

ANGEWANDTE CHEMIE INTERNATIONAL EDITION, Vol. 54, Iss. 28, 2015-07 ,pp. : 8193-8197

John Wiley & Sons Inc

Access to resources Recommend Favorite

Organocatalytic Asymmetric Synthesis of Spiro‐Tetrahydrothiophene Oxindoles Bearing Four Contiguous Stereocenters by One‐Pot Michael–Henry‐Cascade–Rearrangement Reactions

CHEMISTRY - A EUROPEAN JOURNAL, Vol. 24, Iss. 1, 2018-01 ,pp. : 62-66

John Wiley & Sons Inc

Access to resources Recommend Favorite

Cover Feature: Organocatalytic Asymmetric Synthesis of Spiro‐Tetrahydrothiophene Oxindoles Bearing Four Contiguous Stereocenters by One‐Pot Michael–Henry‐Cascade–Rearrangement Reactions (Chem. Eur. J. 1/2018)

CHEMISTRY - A EUROPEAN JOURNAL, Vol. 24, Iss. 1, 2018-01 ,pp. : 2-2

John Wiley & Sons Inc

Access to resources Recommend Favorite

Organocatalytic Asymmetric Addition of Naphthols and Electron‐Rich Phenols to Isatin‐Derived Ketimines: Highly Enantioselective Construction of Tetrasubstituted Stereocenters

ANGEWANDTE CHEMIE, Vol. 127, Iss. 21, 2015-05 ,pp. : 6418-6422

John Wiley & Sons Inc

Access to resources Recommend Favorite

Organocatalytic Asymmetric Addition of Naphthols and Electron‐Rich Phenols to Isatin‐Derived Ketimines: Highly Enantioselective Construction of Tetrasubstituted Stereocenters

ANGEWANDTE CHEMIE INTERNATIONAL EDITION, Vol. 54, Iss. 21, 2015-05 ,pp. : 6320-6324

John Wiley & Sons Inc

Access to resources Recommend Favorite