A double alkylation—ring closing metathesis approach to spiroimines
作者:Margaret A Brimble、Michael Trzoss
DOI:10.1016/j.tet.2004.04.059
日期:2004.6
As part of a programme directed towards the synthesis of the marine toxins, the spirolides and gymnodimine, a convenient synthesis of the key bicyclic spiroimine ring systems has been developed. The method involves double alkylation of a simple lactam, Grubbs ring closing metathesis of the resultant dialkylated lactam then reduction of the lactam to an imine. (C) 2004 Elsevier Ltd. All rights reserved.
SMOLANOFF, J. R.
作者:SMOLANOFF, J. R.
DOI:——
日期:——
SMOLANOFF, J.
作者:SMOLANOFF, J.
DOI:——
日期:——
LIEBOWITZ S. M.; BELAIR E. J.; WITIAK D. T.; LEDNICER D., EUR. J. MED. CHEM., 21,(1986) N 5, 439-444
作者:LIEBOWITZ S. M.、 BELAIR E. J.、 WITIAK D. T.、 LEDNICER D.
DOI:——
日期:——
Liebowitz; Belair; Witiak, European Journal of Medicinal Chemistry, 1986, vol. 21, # 5, p. 439 - 444