Literature DB >> 1499023

Radical cyclisation of hept-1-enitols.

H Redlich1, W Sudau, A K Szardenings, R Vollerthun.   

Abstract

7-Deoxy-7-iodohept-1-enitols react intramolecularly to give 5-carba analogues of pyranoses (pseudo sugars) by the action of tributyltin hydride, which generates a radical at C-7. The configuration at the new chiral centre depends on the relative orientation of the oxygen functions in the starting material and the pattern of substitution.

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Year:  1992        PMID: 1499023     DOI: 10.1016/0008-6215(92)84055-w

Source DB:  PubMed          Journal:  Carbohydr Res        ISSN: 0008-6215            Impact factor:   2.104


  1 in total

1.  Synthesis of C-linked α-Gal and α-GalNAc-1'-hydroxyalkanes by way of C2 functionality transfer.

Authors:  Ernest G Nolen; Ezra S Hornik; Kendra B Jeans; Weiyu Zhong; Danielle M LaPaglia
Journal:  Tetrahedron Lett       Date:  2021-04-23       Impact factor: 2.032

  1 in total

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