Stereospecific approach to the synthesis of ring-A oxygenated sarpagine indole alkaloids. Total synthesis of the dimeric indole alkaloid P -(+)-dispegatrine and six other monomeric indole alkaloids

Journal of Organic Chemistry

Volumn 78, Issue 13, 2013, Pages 6471-6487

  Edwankar, Chitra R ^a   Edwankar, Rahul V ^a   Namjoshi, Ojas A ^a   Liao, Xuebin ^a   Cook, James M ^a  

^a UNIVERSITY OF WISCONSIN MILWAUKEE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ASYMMETRIC INDUCTION; AXIAL CHIRALITY; INDOLE ALKALOIDS; OXIDATIVE DEHYDRODIMERIZATION; REACTION VESSEL; STEREOCONTROL; STEREOSPECIFIC; TOTAL SYNTHESIS;

AMINO ACIDS; DIMERS; METABOLITES; NITROGEN COMPOUNDS; POLYCYCLIC AROMATIC HYDROCARBONS; SYNTHESIS (CHEMICAL); X RAY CRYSTALLOGRAPHY;

ALKALOIDS;

10 METHOXYVELLOSIMINE; ALKALOID DERIVATIVE; CARBOLINE DERIVATIVE; DIMER; DISPEGATRINE; INDOLE DERIVATIVE; LOCHNERAM; LOCHNERINE; LOCHVINERINE; MONOMER; SARPAGINE; SPEGATRINE; UNCLASSIFIED DRUG; ALKALOID; INDOLE ALKALOID; OXYGEN;

ANNULATION REACTION; ARTICLE; CHIRALITY; DIMERIZATION; DRUG SYNTHESIS; HALOGENATION; STEREOSPECIFICITY; STRUCTURE ACTIVITY RELATION; X RAY CRYSTALLOGRAPHY; CHEMICAL STRUCTURE; CHEMISTRY; STEREOISOMERISM; SYNTHESIS;

ALKALOIDS; INDOLE ALKALOIDS; MOLECULAR STRUCTURE; OXYGEN; STEREOISOMERISM;

EID: 84880020998     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo400469t     Document Type: Article

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