Total synthesis of (-)- N -methylwelwitindolinone b isothiocyanate via a chlorinative oxabicycle ring-opening strategy

Journal of the American Chemical Society

Volumn 136, Issue 42, 2014, Pages 14710-14713

  Weires, Nicholas A ^a   Styduhar, Evan D ^a   Baker, Emma L ^a   Garg, Neil K ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ISOTHIOCYANATES; RING OPENING; TOTAL SYNTHESIS;

ALDEHYDE; ALKENE; CARBAMIC ACID; CHLORIDE; INDOLE DERIVATIVE; ISOTHIOCYANIC ACID DERIVATIVE; KETONE; MESYLIC ACID; METHYL GROUP; NUCLEOPHILE; VINYL DERIVATIVE; FUSED HETEROCYCLIC RINGS; INDOLE ALKALOID; ISOTHIOCYANIC ACID; WELWITINDOLINONE B ISOTHIOCYANATE;

ARTICLE; CHLORINATION; CYCLIZATION; DECOMPOSITION; DESILYLATION; DIASTEREOISOMER; EPIMER; HYDROLYSIS; ISOMER; OXIDATION; RING OPENING; SYNTHESIS; CHEMISTRY; CONFORMATION; HALOGENATION; MOLECULAR MODEL;

BRIDGED BICYCLO COMPOUNDS, HETEROCYCLIC; CHEMISTRY TECHNIQUES, SYNTHETIC; HALOGENATION; INDOLE ALKALOIDS; ISOTHIOCYANATES; MODELS, MOLECULAR; MOLECULAR CONFORMATION;

EID: 84908374827     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja5087672     Document Type: Article

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