Preparation and conversion of chiral O-isopropylidene-protected 4-aminocyclohexenol to various key intermediates toward narcissus alkaloids

DSpace CRIS

Please use this identifier to cite or link to this item: http://hdl.handle.net/11455/71434

標題:	Preparation and conversion of chiral O-isopropylidene-protected 4-aminocyclohexenol to various key intermediates toward narcissus alkaloids
作者:	Elango, S. Wang, Y.C. Cheng, C.L. Yan, T.H.
關鍵字:	stereospecific synthesis;microbial oxidation;(+)-pancratistatin;(+)-lycoricidine;aminocyclitols;aromatics
Project:	Tetrahedron Letters
期刊/報告no：:	Tetrahedron Letters, Volume 43, Issue 20, Page(s) 3757-3759.
摘要:	Enantiomerically pure 4-amino-5,6-O-isopropylidenedioxycyclohex-2-en-1-ol, conveniently prepared by the union of O-isopropylidenedioxycyclohexadiene with camphor-based chloronitroso ester, was employed in the synthesis of versatile key intermediates toward narcissus alkaloids. (C) 2002 Elsevier Science Ltd. All rights reserved.
URI:	http://hdl.handle.net/11455/71434
ISSN:	0040-4039
DOI:	10.1016/s0040-4039(02)00543-9
Appears in Collections:	期刊論文

Show full item record

TAIR Related Article

Check