Literature DB >> 11263910

Versatile synthons for optically pure alpha-amino aldehydes and alpha-amino acids: (+)- and (-)-4,5-dialkoxy-2-oxazolidinones.

T Morita1, Y Nagasawa, S Yahiro, H Matsunaga, T Kunieda.   

Abstract

Both enantiomers of trans-5-benzyloxy-4-methoxy- (BMOx) and trans-4,5-dimethoxy-2-oxazolidinones (DMOx), which are readily accessible from simple 2-oxazolone heterocycles, represent good candidates for a new class of chiral synthons for use in the preparation of optically pure alpha-amino aldehydes and alpha-amino acids, respectively.

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Year:  2001        PMID: 11263910     DOI: 10.1021/ol015535r

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


  1 in total

1.  Hypervalent iodine/TEMPO-mediated oxidation in flow systems: a fast and efficient protocol for alcohol oxidation.

Authors:  Nida Ambreen; Ravi Kumar; Thomas Wirth
Journal:  Beilstein J Org Chem       Date:  2013-07-17       Impact factor: 2.883

  1 in total

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