Application of the aza-Achmatowicz oxidative rearrangement for the stereoselective synthesis of the Cassia and Prosopis alkaloid family

Journal of Organic Chemistry

Volumn 71, Issue 22, 2006, Pages 8591-8601

  Leverett, Carolyn A ^a   Cassidy, Michael P ^a   Padwa, Albert ^a  

^a EMORY UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOLS; CATALYSIS; OXIDATION; REDUCTION; STEREOCHEMISTRY; SYNTHESIS (CHEMICAL);

AZIMIC ACID; DIHYDROPYRIDONE REDUCTION; PROSOPIS ALKALOIDS; STEREOSELECTIVE SYNTHESIS;

AMINES;

6 ETHOXY 2 METHYL 1 (TOLUENE 4 SULFONYL) 1,6 DIHYDRO 2H PYRIDIN 3 ONE; ALKALOID DERIVATIVE; AZIMIC ACID; CASSINE; DEOXOCASSINE; N TOSYLAMIDOFURAN; PIPERIDINE DERIVATIVE; PYRIDONE DERIVATIVE; SILANE DERIVATIVE; SPICIGERINE; TOLUENESULFONIC ACID DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL ANALYSIS; CHEMICAL REACTION; CHEMICAL STRUCTURE; DRUG SYNTHESIS; NONHUMAN; OXIDATION REDUCTION REACTION; PROSOPIS; SENNA; STEREOCHEMISTRY; STEREOSPECIFICITY;

ALKALOIDS; CASSIA; MOLECULAR STRUCTURE; OXIDATION-REDUCTION; PROSOPIS; STEREOISOMERISM;

EID: 33750453788     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo0616714     Document Type: Article

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