One-pot synthesis of N-acyl-substituted sulfamides from chlorosulfonyl isocyanate via the Burgess-type intermediates

Tetrahedron Letters

Volumn 45, Issue 9, 2004, Pages 1853-1856

  Masui, Yoshiyuki ^a   Watanabe, Hideaki ^a   Masui, Toshiaki ^a  

^a SHIONOGI AND CO LTD   (Japan)

Author keywords

Burgess reagent; Chlorosulfonyl isocyanate; Sulfamides

Indexed keywords

ALCOHOL DERIVATIVE; AMINE; AMMONIUM DERIVATIVE; CARBAMIC ACID DERIVATIVE; CARBONYL DERIVATIVE; CHLOROSULFONYL ISOCYANATE; ISOCYANIC ACID DERIVATIVE; SULFANILAMIDE; SULFONE DERIVATIVE; UNCLASSIFIED DRUG; WATER;

AQUEOUS SOLUTION; ARTICLE; SPECTROSCOPY; SYNTHESIS;

EID: 1242271372     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2004.01.008     Document Type: Article

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24. For example, n-butanethiol gave N-(1-butylthiocarbonyl)sulfamide ( 9 ) in 80% yield: Masui Y.; Watanabe, H., in preparation.