Abstract
The thiazole-thiazoline fragment of the marine natural product largazole, a potent histone deacetylase 1 inhibitor, has been synthesized in five steps. The methodology provides rapid access to thiazole-4-carbonitrile, thiazole-4-carbimidate, thiazole-oxazoline, and other thiazole-thiazoline derivatives that are important intermediates in the total synthesis of many natural products with important biological properties.
Original language | English |
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Journal | Journal of Organic Chemistry |
Volume | 76 |
Issue number | 23 |
Pages (from-to) | 9845-9851 |
ISSN | 0022-3263 |
DOIs | |
Publication status | Published - 2 Dec 2011 |
Keywords
- Former Faculty of Pharmaceutical Sciences