Catalytic, Asymmetric Halofunctionalization of Alkenes-A Critical Perspective

被引:501
作者
Denmark, Scott E. [1 ]
Kuester, William E. [1 ]
Burk, Matthew T. [1 ]
机构
[1] Univ Illinois, Dept Chem, Urbana, IL 61801 USA
基金
美国国家卫生研究院;
关键词
alkenes; halogenation; homogeneous catalysis; Lewis base; synthetic methods; HALONIUM ION FORMATION; STABLE CARBONIUM-IONS; NEIGHBORING HALOGEN PARTICIPATION; HIGHLY EFFICIENT SYNTHESIS; BRONSTED ACID CATALYST; LEWIS-BASE CATALYSIS; ENANTIOSELECTIVE BROMOLACTONIZATION; MECHANISTIC EVALUATION; HALOCYCLIZATION; COMPLEXES;
D O I
10.1002/anie.201204347
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Despite the fact that halogenation of alkenes has been known for centuries, enantioselective variants of this reaction have only recently been developed. In the past three years, catalytic enantioselective versions of halofunctionalizations with the four common halogens have appeared and although important breakthroughs, they represent just the very beginnings of a nascent field. This Minireview provides a critical analysis of the challenges that accompany the development of general and highly enantioselective halofunctionalization reactions. Moreover, the focus herein, diverges from previous reviews of the field by identifying the various modes of catalysis and the different strategies implemented for asymmetric induction. The return of the salt makers: Catalytic enantioselective versions of halofunctionalizations have recently appeared and although important breakthroughs, they represent just the very beginnings of a nascent field. Herein is a critical analysis of the challenges that accompany the development of general and highly enantioselective halofunctionalizations. Various modes of catalysis and the different strategies implemented for asymmetric induction are identified. Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
引用
收藏
页码:10938 / 10953
页数:16
相关论文
共 105 条
[51]  
Jiang X., 2012, ANGEW CHEM, V124, P7891
[52]   Enantioselective Bromolactonization Using an S-Alkyl Thiocarbamate Catalyst [J].
Jiang, Xiaojian ;
Tan, Chong Kiat ;
Zhou, Ling ;
Yeung, Ying-Yeung .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2012, 51 (31) :7771-7775
[53]   Asymmetric iodocyclization of γ-hydroxyalkenes [J].
Kang, SH ;
Park, CM ;
Lee, SB ;
Kim, M .
SYNLETT, 2004, (07) :1279-1281
[54]   Catalytic enantioselective lodocyclization of γ-hydroxy-cis-alkenes [J].
Kang, SH ;
Lee, SB ;
Park, CM .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (51) :15748-15749
[55]   ENANTIOSELECTIVE HALOCYCLIZATION REACTION USING A CHIRAL TITANIUM COMPLEX [J].
KITAGAWA, O ;
HANANO, T ;
TANABE, K ;
SHIRO, M ;
TAGUCHI, T .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1992, (14) :1005-1007
[56]   Synthesis of TRIP and Analysis of Phosphate Salt Impurities [J].
Klussmann, Martin ;
Ratjen, Lars ;
Hoffmann, Sebastian ;
Wakchaure, Vijay ;
Goddard, Richard ;
List, Benjamin .
SYNLETT, 2010, (14) :2189-2192
[57]   CATALYTIC ASYMMETRIC DIHYDROXYLATION [J].
KOLB, HC ;
VANNIEUWENHZE, MS ;
SHARPLESS, KB .
CHEMICAL REVIEWS, 1994, 94 (08) :2483-2547
[58]   Asymmetric iodocyclization catalyzed by Salen-CrIII Cl:: Its synthetic application to swainsonine [J].
Kwon, Hyo Young ;
Park, Chul Min ;
Lee, Sung Bae ;
Youn, Joo-Hack ;
Kang, Sung Ho .
CHEMISTRY-A EUROPEAN JOURNAL, 2008, 14 (03) :1023-1028
[59]   What is the nature of the first-formed intermediates in the electrophilic halogenation of alkenes, alkynes, and allenes? [J].
Lenoir, D ;
Chiappe, C .
CHEMISTRY-A EUROPEAN JOURNAL, 2003, 9 (05) :1036-1044
[60]   First asymmetric intermolecular bromoesterification catalyzed by chiral Bronsted acid [J].
Li, Guang-xun ;
Fu, Qing-quan ;
Zhang, Xiao-mei ;
Jiang, Jun ;
Tang, Zhuo .
TETRAHEDRON-ASYMMETRY, 2012, 23 (3-4) :245-251