ChemInform Abstract: The Taumycin A Macrocycle: Asymmetric Total Synthesis and Revision of Relative Stereochemistry

The relative stereochemistry of the taumycin macrolide is confirmed via the first total synthesis of taumycin aldehyde (I).

Saved in:
Bibliographic Details
Published inChemInform Vol. 46; no. 14; p. no
Main Authors deGruyter, Justine N., Maio, William A.
Format Journal Article
LanguageEnglish
Published Weinheim WILEY-VCH Verlag 01.04.2015
WILEY‐VCH Verlag
Wiley Subscription Services, Inc
Subjects
amino acids
amino acids, peptides, proteins
peptides
proteins
structure (organic substances)
Online AccessGet full text

Cover

More Information
Summary:The relative stereochemistry of the taumycin macrolide is confirmed via the first total synthesis of taumycin aldehyde (I).
Bibliography:ark:/67375/WNG-LVM5VRZH-2
ArticleID:CHIN201514258
istex:6971F8617A10545FBB547DDA732FD2F32714A380
ISSN:0931-7597
1522-2667
DOI:10.1002/chin.201514258