Literature DB >> 18698647

An effective route to fluorine containing asymmetric alpha-aminophosphonates using chiral Bronsted acid catalyst.

Pinaki S Bhadury1, Yuping Zhang, Sha Zhang, Baoan Song, Song Yang, Deyu Hu, Zhuo Chen, Wei Xue, Linhong Jin.   

Abstract

Asymmetric addition of dialkyl phosphites (--CH2CH3, --CH2CH2CH3, --CH(CH3)2, --CH2(CH2)3CH3, --CH2CH2OCH3 and --CH2CH2OC2H5) induced by chiral organocatalyst e.g. (R)- and (S)-3,3'-[3,5-bis(trifluoromethyl)phenyl]2-1,1'-binaphthyl phosphate on fluorinated aldimines derived from cinnamaldehyde has been found effective to give new bioactive alpha-aminophosphonates in good yields (58-73%) and high enantiomeric excess (64.6%-90.6%) under mild conditions.

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Year:  2009        PMID: 18698647     DOI: 10.1002/chir.20645

Source DB:  PubMed          Journal:  Chirality        ISSN: 0899-0042            Impact factor:   2.437


  1 in total

1.  Asymmetric synthesis of alpha-aminophosphonates using the inexpensive chiral catalyst 1,1'-binaphthol phosphate.

Authors:  Weiming Xu; Sha Zhang; Song Yang; Lin-Hong Jin; Pinaki S Bhadury; De-Yu Hu; Yuping Zhang
Journal:  Molecules       Date:  2010-08-24       Impact factor: 4.411

  1 in total

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