Lithiation-induced migrations from nitrogen to carbon in terminal aziridines

Lithiation-induced migrations from nitrogen to carbon in terminal aziridines
复制标题

DOI:
10.1002/anie.200604920
复制
发表时间:
2007-01-01
影响因子:
16.6
通讯作者:
Ward, John G.
Ward, John G.
中科院分区:
化学1区
文献类型:
--
作者:
Hodgson, David M.;Humphreys, Philip G.;Ward, John G.

文献摘要

被引文献

相似文献

受益于去保护:2,2,6,6-四甲基哌啶酸锂诱导N-Boc或n -膦酸末端的氮基进行区域和立体选择性的n -到- c迁移,得到有合成价值的反式氮基酰基酯和反式氮基膦酸盐。©2007 Wiley-VCH Verlag GmbH and Co. KGaA。
(Chemical Equation Presented) Benefiting from deprotection: Lithium 2,2,6,6-tetramethylpiperidide induces N-Boc or N-phosphonate terminal aziridines to undergo regio- and stereoselective N-to-C migration of the protecting group, giving synthetically valuable trans-aziridinylesters and trans- aziridinylphosphonates. © 2007 Wiley-VCH Verlag GmbH and Co. KGaA.