Predominant Conformations of (2R,3R)-(−)-2,3-Butanediol
Author:
Affiliation:
1. Department of Chemistry, Vanderbilt University, Nashville, TN37235
Publisher
American Chemical Society (ACS)
Subject
Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jp010550z
Reference25 articles.
1. Conformation in the solid state and in solution of (9R, 10R, 21R,-22R)-9, 10, 21, 22-Tetramethyl-9, 10, 21, 22-tetrahydro-7H, 12H,-19H, 24H-dinaphtho-[1, 8-f, g: 1′, 8′o, p][1.4.10.13]- tetraoxacyclooctadecin
2. Asymmetric synthesis of N-acetyl-1-phenylethylamine
3. Synthesis of All Four Possible Stereoisomers of 1-Phenyl-2,3-butanediol and Both Enantiomers of 3-Hydroxy-4-phenyl-2-butanone to Determine the Absolute Configuration of the Natural Constituents
4. Synthesis of d- and 1-sirenin and their absolute configurations
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