期刊
TETRAHEDRON LETTERS
卷 52, 期 42, 页码 5435-5437出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2011.07.128
关键词
Hantzsch cyclization; Thiazole; Thiopeptides; Proline
资金
- Ministerio de Ciencia e Innovacion, CICYT [CTQ2009-07758]
- Generalitat de Catalunya [2009SGR 1024]
- ISCIII
- Ministerio de Ciencia e Innovacion
(S)-2-(4-Bromo-2,4'-bithiazole)-1-(tert-butoxycarbonyl)pyrrolidine ((S)-1) was obtained as a single enantiomer and in high yield by means of a two-step modified Hantzsch thiazole synthesis reaction when bromoketone 3 and thioamide (S)-4 were used. Further conversion of (S)-1 into trimethyltin derivative (S)-2 broadens the scope for further cross-coupling reactions. (C) 2011 Elsevier Ltd. All rights reserved.
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