Literature DB >> 10810730

Aldol reaction under solvent-free conditions: highly stereoselective synthesis of 1,3-amino alcohols

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Abstract

[formula: see text] A method for the highly stereoselective synthesis of 1,3-amino alcohols based on the indium trichloride-catalyzed Mukaiyama aldol reaction of keto ester (R,S)-1 under solvent-free conditions has been developed. The high selectivity observed can be explained on the basis of the shielding of one face by a remote substituent.

Entities:  

Year:  2000        PMID: 10810730     DOI: 10.1021/ol000042s

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  2 in total

1.  An efficient protocol for the synthesis of highly sensitive indole imines utilizing green chemistry: optimization of reaction conditions.

Authors:  Bushra Nisar; Syeda Laila Rubab; Abdul Rauf Raza; Sobia Tariq; Ayesha Sultan; Muhammad Nawaz Tahir
Journal:  Mol Divers       Date:  2018-04-11       Impact factor: 2.943

2.  Solvent-Free and Efficient One-Pot Strategy for Synthesis of the Triazine-Heterocycle Azacyanines.

Authors:  Xianwu Jiang; Zhuodong Sun; Yu Wang
Journal:  Materials (Basel)       Date:  2022-04-02       Impact factor: 3.623

  2 in total

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