Literature DB >> 17312977

N-alkyl oxazolidines as stereocontrol elements in asymmetric Diels-Alder cycloadditions of 9-substituted anthracene derivatives.

Harry Adams1, Ramadan A Bawa, Simon Jones.   

Abstract

Chiral 9-oxazolidinyl anthracene derivatives have been prepared as single diastereoisomers by condensation of 9-anthraldehyde with the appropriate N-alkyl amino alcohol. Asymmetric Diels-Alder cycloadditions of these with N-methyl maleimide proceeds in good yield and in good diastereoselectivity, the sense of which may be controlled by judicious choice of the N-alkyl group.

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Year:  2006        PMID: 17312977     DOI: 10.1039/b610055d

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  1 in total

1.  17-Hy-droxy-1,8-dimethyl-17-aza-penta-cyclo-[6.6.5.0(2,7).0(9,14).0(15,19)]nona-deca-2,4,6,9(14),10,12-hexa-ene-16,18-dione.

Authors:  Barbara Miroslaw; Anna E Koziol; Magdalena Pakosinska-Parys; Marta Struga
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2012-11-07
  1 in total

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