Direct synthesis of functionalized unsymmetrical β-sulfonamido disulfides by tetrathiomolybdate mediated aziridine ring-opening reactions

Journal of Organic Chemistry

Volumn 74, Issue 20, 2009, Pages 7958-7961

  Sureshkumar, Devarajulu ^a   Ganesh, Venkataraman ^a   Vidyarini, Ravindran Sasitha ^a   Chandrasekaran, Srinivasan ^b  

^a INDIAN INSTITUTE OF SCIENCE   (India)

^b JAWAHARLAL NEHRU CENTRE FOR ADVANCED SCIENTIFIC RESEARCH   (India)

Author keywords

[No Author keywords available]

Indexed keywords

AZIRIDINE RING; AZIRIDINES; CHEMICAL EQUATIONS; DIRECT SYNTHESIS; ELECTRON-DONATING SUBSTITUENTS; FUNCTIONALIZED; GOOD YIELD; RING OPENING; SULFUR TRANSFER; TETRATHIOMOLYBDATE; UNSYMMETRICAL;

AROMATIC HYDROCARBONS; IONIC LIQUIDS; SULFUR; SYNTHESIS (CHEMICAL);

STEEL BEAMS AND GIRDERS;

ALLICIN; AZIRIDINE; BETA SULFONAMIDO DISULFIDE; DISULFIDE; PHENYLALANINE; SULFUR; SULFURTRANSFERASE; TETRATHIOMOLYBDATE AMMONIUM; TETRATHIOMOLYBDIC ACID; UNCLASSIFIED DRUG;

ARTICLE; DISULFIDE BOND; ELECTRON; RING OPENING; SUBSTITUTION REACTION; SYNTHESIS;

AZIRIDINES; DISULFIDES; MOLECULAR STRUCTURE; MOLYBDENUM; SULFONAMIDES;

EID: 70349878328     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo901528e     Document Type: Article

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