A new, stereoselective, ring-forming reaction of 1,2-ethanedithiol with N-acylated indoles

Journal of Organic Chemistry

Volumn 72, Issue 23, 2007, Pages 8928-8931

  Tsotinis, Andrew ^a,b   Eleutheriades, Andreas ^a,b   Di Bari, Lorenzo ^b   Pescitelli, Gennaro ^b  

^a UNIVERSITY OF ATHENS   (Greece)

^b UNIVERSITY OF PISA   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

3,6-DITHIAAZEPINE RING; ANNELATION; N-ACYL 5-FLUOROINDOLE; N-ACYLINDOLES;

DERIVATIVES; NITROGEN COMPOUNDS; STEREOSELECTIVITY;

REACTION KINETICS;

1,2 ETHANEDITHIOL; 2,5 DITHIACYCLOPENTYL DERIVATIVE; 3,6 DITHIAAZEPINE; AZEPINE DERIVATIVE; INDOLE DERIVATIVE; N ACYL 5 FLUOROINDOLE; THIOL DERIVATIVE; UNCLASSIFIED DRUG;

ACYLATION; ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; REACTION ANALYSIS; STEREOCHEMISTRY; SYNTHESIS;

CYCLIZATION; INDOLES; MAGNETIC RESONANCE SPECTROSCOPY; MERCAPTOETHANOL; MODELS, MOLECULAR; MOLECULAR STRUCTURE; REFERENCE STANDARDS; STEREOISOMERISM; SULFHYDRYL COMPOUNDS;

EID: 35948950154     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo7013142     Document Type: Article

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