Iridium(iii)-bis(imidazolinyl)phenyl catalysts for enantioselective C-H functionalization with ethyl diazoacetate.

Iridium(iii)-bis(imidazolinyl)phenyl catalysts for enantioselective C-H functionalization with ethyl diazoacetate.
复制标题

DOI:
10.1039/c6sc00190d
复制
发表时间:
2016-05-01
期刊:
影响因子:
8.4
通讯作者:
Blakey SB
Blakey SB
中科院分区:
化学1区
文献类型:
--
作者:
Weldy NM;Schafer AG;Owens CP;Herting CJ;Varela-Alvarez A;Chen S;Niemeyer Z;Musaev DG;Sigman MS;Davies HML;Blakey SB

文献摘要

参考文献

被引文献

相似文献

利用一类新的Ir(iii)-双(咪唑啉基)苯基催化剂,报道了仅受体金属羰基的分子间对映选择性C-H功能化反应。利用一种新的Ir(iii)-双(咪唑啉基)苯基催化剂家族,基于实验和计算见解的相互作用,报道了仅受体金属羰基的分子间对映选择性C-H功能化。该反应对多种重氮乙酸前体具有耐受性,并且发现底物的空间和电子性质对该反应有很大影响。邻苯二甲酸和二氢呋喃衍生物具有良好的产率和对映选择性。
The intermolecular enantioselective C–H functionalization with acceptor-only metallocarbenes is reported using a new family of Ir(iii)-bis(imidazolinyl)phenyl catalysts. The intermolecular enantioselective C–H functionalization with acceptor-only metallocarbenes is reported using a new family of Ir(iii)-bis(imidazolinyl)phenyl catalysts, developed based on the interplay of experimental and computational insights. The reaction is tolerant of a variety of diazoacetate precursors and is found to be heavily influenced by the steric and electronic properties of the substrate. Phthalan and dihydrofuran derivatives are functionalized in good yields and excellent enantioselectivities.
DOI: 10.1002/anie.201310544
发表时间: 2014-02-17
影响因子: 16.6
作者:
Kim, Jinwoo;Chang, Sukbok
通讯作者: Chang, Sukbok
DOI: 10.1021/ja016798j
发表时间: 2002-02-13
影响因子: 15
作者:
Díaz-Requejo, MM;Belderraín, TR;Pérez, PJ
通讯作者: Pérez, PJ
DOI: 10.1016/j.tetlet.2006.05.096
发表时间: 2006-07-17
影响因子: 1.8
作者:
Hao, Xin-Qi;Gong, Jun-Fang;Song, Mao-Ping
通讯作者: Song, Mao-Ping
DOI: 10.1002/adsc.200606049
发表时间: 2006-07-01
影响因子: 5.4
作者:
Ito, Jun-ichi;Shiomi, Takushi;Nishiyama, Hisao
通讯作者: Nishiyama, Hisao
DOI: 10.1039/c39810000688
发表时间: 1981-01-01
影响因子: --
作者:
DEMONCEAU, A;NOELS, AF;TEYSSIE, P
通讯作者: TEYSSIE, P