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

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