A new magnesium-catalyzed doubly diastereoselective anti-aldol reaction leads to a highly efficient process for the total synthesis of lactacystin in quantity

Journal of the American Chemical Society

Volumn 120, Issue 10, 1998, Pages 2330-2336

  Corey, E J ^a   Li, Weidong ^a   Reichard, Gregory A ^a  

^a HARVARD UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BETA LACTONE; LACTACYSTIN; MAGNESIUM; MICROBIAL PRODUCTS NOT CLASSIFIED ELSEWHERE; UNCLASSIFIED DRUG;

ARTICLE; CATALYST; CELL DIFFERENTIATION; CHROMATOGRAPHY; CONTROLLED STUDY; DRUG ACTIVITY; NEUROBLASTOMA CELL; NONHUMAN; QUANTITATIVE ASSAY; STEREOCHEMISTRY; SYNTHESIS; TECHNIQUE;

EID: 0032542772     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja973444c     Document Type: Article

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