Reaction of α-halo ketone with 2-aminothiol: a new synthesis of thiazolidines with the oxo group migrated to the original position occupied by halogen atom

Tetrahedron

Volumn 63, Issue 36, 2007, Pages 8932-8938

  Matsushita, Masatoshi ^a   Takahashi, T Tomoyoshi ^b   Utsukihara, Takamitsu ^a   Shimizu, Yohei ^a   Jansen, Rob J ^c   Horiuchi, C Akira ^a  

^a RIKKYO UNIVERSITY   (Japan)

^b JIKEI UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^c RADBOUD UNIVERSITY NIJMEGEN   (Netherlands)

Author keywords

Bromo ketone; 1 Thia 4 azaspiro 4.5 decan 6 one; 2 Aminoethanethiol; Condensation; Microwave; Spiro steroid 3,2 thiazolidine s

Indexed keywords

2 BROMO 3 OXO STEROID; ALPHA HALO KETONE; KETONE; MERCAPTAMINE; SPIRO[5ALPHA CHOLESTAN 3,2' THIAZOLIDIN] 2 ONE; SPIRO[5ALPHA LANOST 8 EN 3,2' THIAZOLIDIN] 2 ONE; SPIRO[5BETA CHOLESTAN 3,2' THIAZOLIDIN] 2 ONE; SPIRO[5BETA CHOLESTAN 3,2' THIAZOLIDIN] 4 ONE; SPIRO[STEROID 3,2' THIAZOLIDIN] 2 ONE DERIVATIVE; STEROID; THIAZOLIDINE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; DRUG STRUCTURE; DRUG SYNTHESIS; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE;

THIA;

EID: 34447635262     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2007.06.041     Document Type: Article

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