Protecting‐Group‐Free Enantioselective Synthesis of (−)‐Pallavicinin and (+)‐Neopallavicinin

Publisher： John Wiley & Sons Inc

E-ISSN： 1521-3773|54|46|13599-13603

ISSN： 1433-7851

Source： ANGEWANDTE CHEMIE INTERNATIONAL EDITION, Vol.54, Iss.46, 2015-11, pp. : 13599-13603

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

Protecting‐Group‐Free Enantioselective Synthesis of (−)‐Pallavicinin and (+)‐Neopallavicinin

By  

ANGEWANDTE CHEMIE, Vol. 127, Iss. 46, 2015-11 ,pp. : 13803-13807

John Wiley & Sons Inc

Access to resources Recommend Favorite

Synthesis of Monodisperse Sequence‐Defined Polymers Using Protecting‐Group‐Free Iterative Strategies

By  

MACROMOLECULAR CHEMISTRY AND PHYSICS, Vol. 216, Iss. 14, 2015-07 ,pp. : 1498-1506

John Wiley & Sons Inc

Access to resources Recommend Favorite

Atom‐Economical Dimerization Strategy by the Rhodium‐Catalyzed Addition of Carboxylic Acids to Allenes: Protecting‐Group‐Free Synthesis of Clavosolide A and Late‐Stage Modification

By  

ANGEWANDTE CHEMIE, Vol. 127, Iss. 51, 2015-12 ,pp. : 15750-15754

John Wiley & Sons Inc

Access to resources Recommend Favorite

Catalyst‐Directed Diastereo‐ and Site‐Selectivity in Successive Nucleophilic and Electrophilic Allylations of Chiral 1,3‐Diols: Protecting‐Group‐Free Synthesis of Substituted Pyrans

By  

CHEMISTRY - A EUROPEAN JOURNAL, Vol. 20, Iss. 41, 2014-10 ,pp. : 13382-13389

John Wiley & Sons Inc

Access to resources Recommend Favorite

Atom‐Economical Dimerization Strategy by the Rhodium‐Catalyzed Addition of Carboxylic Acids to Allenes: Protecting‐Group‐Free Synthesis of Clavosolide A and Late‐Stage Modification

By  

ANGEWANDTE CHEMIE INTERNATIONAL EDITION, Vol. 54, Iss. 51, 2015-12 ,pp. : 15530-15534

John Wiley & Sons Inc

Access to resources Recommend Favorite