Literature DB >> 19826667

Synthesis of a new spiro-BOX ligand and its application in enantioselective allylic cyclization based on carbopalladation of allenyl hydrazines.

Wei Shu1, Shengming Ma.   

Abstract

In this paper, we developed a new bisoxazoline ligand with a spiro skeleton and a alpha-naphthylmethyl substituent, i.e. (Ra,S,S)-L3, which has been successfully applied to the highly enantioselective cyclic allylation based on the carbopalladation of 3,4-allenyl hydrazines with ee values ranging from 92-95%.

Entities:  

Year:  2009        PMID: 19826667     DOI: 10.1039/b912108k

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  3 in total

1.  A catalytic highly enantioselective allene approach to oxazolines.

Authors:  Hongwen Luo; Zheng Yang; Weilong Lin; Yangguangyan Zheng; Shengming Ma
Journal:  Chem Sci       Date:  2018-01-05       Impact factor: 9.825

2.  Palladium-Catalyzed, Enantioselective Formal Cycloaddition between Benzyltriflamides and Allenes: Straightforward Access to Enantioenriched Isoquinolines.

Authors:  Xandro Vidal; José L Mascareñas; Moisés Gulías
Journal:  J Am Chem Soc       Date:  2019-01-22       Impact factor: 15.419

3.  Organocatalytic cascade aza-Michael/hemiacetal reaction between disubstituted hydrazines and α,β-unsaturated aldehydes: Highly diastereo- and enantioselective synthesis of pyrazolidine derivatives.

Authors:  Zhi-Cong Geng; Jian Chen; Ning Li; Xiao-Fei Huang; Yong Zhang; Ya-Wen Zhang; Xing-Wang Wang
Journal:  Beilstein J Org Chem       Date:  2012-10-09       Impact factor: 2.883

  3 in total

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