Intramolecular nucleophilic addition of carbanions generated from N-benzylamides to cyclopropenes.

Intramolecular nucleophilic addition of carbanions generated from N-benzylamides to cyclopropenes.
复制标题

DOI:
10.1039/c7ob02068f
复制
发表时间:
2018-01-03
影响因子:
3.2
通讯作者:
Rubin M
Rubin M
中科院分区:
化学3区
文献类型:
--
作者:
Maslivetc V;Barrett C;Aksenov NA;Rubina M;Rubin M

文献摘要

参考文献

被引文献

相似文献

Unusual reaction is described, involving a formal intramolecular nucleophilic substitution of bromocyclopropanes with nitrogen ylides generated in situ from N-benzyl carboxamides. It is shown that this reaction involves cyclopropene intermediates and allows for facile and expeditious preparation of 3-azabicyclo[3.1.0]hexan-2-one scaffolds.
DOI: 10.1021/jo200368a
发表时间: 2011-05-20
影响因子: 3.6
作者:
Banning, Joseph E.;Prosser, Anthony R.;Rubin, Michael
通讯作者: Rubin, Michael
DOI: 10.1021/ol8011138
发表时间: 2008-08-07
期刊: ORGANIC LETTERS
影响因子: 5.2
作者:
Alnasleh, Bassam K.;Sherrill, William M.;Rubin, Michael
通讯作者: Rubin, Michael
DOI: 10.1016/s0040-4039(02)00154-5
发表时间: 2002-03-11
影响因子: 1.8
作者:
Bragg, RA;Clayden, J;Menet, CJ
通讯作者: Menet, CJ
DOI: 10.1021/ol1029904
发表时间: 2011-02-18
期刊: ORGANIC LETTERS
影响因子: 5.2
作者:
Kraemer, Katja;Leong, Paul;Lautens, Mark
通讯作者: Lautens, Mark
DOI: 10.1016/j.tet.2010.04.123
发表时间: 2010-07-03
期刊: TETRAHEDRON
影响因子: 2.1
作者:
Kim, Ryan;Sherrill, William M.;Rubin, Michael
通讯作者: Rubin, Michael