The total synthesis of (±)-11-O-debenzoyltashironin

Journal of the American Chemical Society

Volumn 128, Issue 51, 2006, Pages 16440-16441

  Cook, Silas P ^a   Polara, Alessandra ^a   Danishefsky, Samuel J ^a,b  

^a Och Spine at New York Presbyterian Hospitals   (United States)

^b MEMORIAL SLOAN KETTERING CANCER CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

11 O DEBENZOYLTASHIRONIN; CARBON; NATURAL PRODUCT; UNCLASSIFIED DRUG; 11-O-DEBENZOYLTASHIRONIN; BRIDGED COMPOUND;

ANNULATION REACTION; AROMATIZATION; ARTICLE; CYCLIZATION; DIELS ALDER REACTION; DRUG ACTIVITY; DRUG SYNTHESIS; NERVE CELL GROWTH; OXIDATION; CHEMICAL STRUCTURE; CHEMISTRY; ILLICIUM; OXIDATION REDUCTION REACTION; STEREOISOMERISM; SYNTHESIS;

BRIDGED COMPOUNDS; ILLICIUM; MOLECULAR STRUCTURE; OXIDATION-REDUCTION; STEREOISOMERISM;

EID: 33845924762     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja0670254     Document Type: Article

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19. The results described herein are part of a much larger study of the tashironin problem, described in the PhD thesis of Silas Cook (Columbia University, 2006). This thesis contains confirmatory crystallographic studies of related compounds, which will be disclosed as part of a full paper.