Asymmetric Epoxidation Provides Shortest Routes to Four Chiral Epoxy Alcohols Which Are Key Intermediates in Syntheses of Methymycin, Erythromycin, Leukotriene C-1, and Disparlure

Journal of the American Chemical Society

Volumn 103, Issue 2, 1981, Pages 464-465

  Rossiter, Bryant E ^a   Katsuki, Tsutomu ^a   Sharpless, K Barry ^a  

^a STANFORD UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DISPARLURE;

DRUG ANALYSIS; DRUG STRUCTURE; DRUG SYNTHESIS; EPOXYALKANE DERIVATIVE; IN VITRO STUDY; POLARIMETRY; PRELIMINARY COMMUNICATION; THEORETICAL STUDY;

EID: 0019424113     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja00392a038     Document Type: Article

References (0)