Studies directed toward the total synthesis of cerorubenic acid-III. 5. A radical cyclization route leading to the methyl ester of the natural isomer

Journal of the American Chemical Society

Volumn 120, Issue 24, 1998, Pages 5953-5960

  Paquette, Leo A ^a  

^a OHIO STATE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CERORUBENIC ACID III; SESTERTERPENE; UNCLASSIFIED DRUG;

ARTICLE; CYCLIZATION; DRUG SYNTHESIS; ENANTIOMER; ISOMER; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; REACTION ANALYSIS; X RAY ANALYSIS;

EID: 0031750234     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja980691n     Document Type: Article

References (2)

1. (a) Part 4: Paquette, L. A.; Hormuth, S.; Lovely, C. J. J. Org. Chem. 1995, 60, 4813.
2. (b) Part 3: Paquette, L. A.; Deaton, D. N.; Endo, Y.; Poupart, M.-A. J. Org. Chem. 1993, 58, 4262.