Extending Pummerer reaction chemistry. Development of a strategy for the regio- and stereoselective oxidative cyclization of 3-(ω-nucleophile)- tethered indoles

Journal of Organic Chemistry

Volumn 70, Issue 16, 2005, Pages 6429-6440

  Feldman, Ken S ^a   Vidulova, Daniela Boneva ^a   Karatjas, Andrew G ^a  

^a PENNSYLVANIA STATE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CARBOXYLATION; DERIVATIVES; OXIDATION; STEREOCHEMISTRY; SUBSTRATES; SULFUR COMPOUNDS;

INDOLES; PUMMERER REACTION CHEMISTRY; REGIOCHEMISTRY; SILYLOXY SUBSTITUENT;

REACTION KINETICS;

ALLYLSILANE; BETA SILYLOXYTRYPTOPHAN DERIVATIVE; CARBON; CARBOXYLIC ACID; ETHER; INDOLE DERIVATIVE; KETENE DERIVATIVE; OXINDOLE; SILICON DERIVATIVE; SILYL ETHER; SILYL KETENE; SULFIDE; SULFOXIDE; TRYPTOPHAN DERIVATIVE; UNCLASSIFIED DRUG;

ADDITION REACTION; ARTICLE; BROMINATION; CHEMISTRY; CYCLIZATION; DIASTEREOISOMER; OXIDATION; PUMMERER REACTION; REGIOSELECTIVITY; STEREOCHEMISTRY;

CYCLIZATION; ELECTRONS; ETHYLENES; INDOLES; KETONES; MOLECULAR STRUCTURE; OXIDATION-REDUCTION; STEREOISOMERISM; TRYPTOPHAN;

EID: 23044492191     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo050896w     Document Type: Article

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