Benzothiazines in synthesis. Formal syntheses of (+)-curcumene and (+)-curcuphenol
摘要:
A benzothiazine readily available in enantiomerically pure form via a stereoselective, intramolecular Michael addition reaction could be converted to a precursor to (+)-curcuphenol and to (+)-curcumene. (C) 2003 Elsevier Ltd. All rights reserved.
Benzothiazines in synthesis. Formal syntheses of (+)-curcumene and (+)-curcuphenol
摘要:
A benzothiazine readily available in enantiomerically pure form via a stereoselective, intramolecular Michael addition reaction could be converted to a precursor to (+)-curcuphenol and to (+)-curcumene. (C) 2003 Elsevier Ltd. All rights reserved.
Benzothiazines in synthesis. Formal syntheses of (+)-curcumene and (+)-curcuphenol
作者:Michael Harmata、Xuechuan Hong、Charles L Barnes
DOI:10.1016/s0040-4039(03)01882-3
日期:2003.9
A benzothiazine readily available in enantiomerically pure form via a stereoselective, intramolecular Michael addition reaction could be converted to a precursor to (+)-curcuphenol and to (+)-curcumene. (C) 2003 Elsevier Ltd. All rights reserved.