The 2x3 toolbox of organometallic methods for regiochemically exhaustive functionalization

被引:281
作者
Schlosser, M [1 ]
机构
[1] Ecole Polytech Fed Lausanne, Inst Chem Sci, ISIS, CH-1015 Lausanne, Switzerland
[2] Univ Lausanne, Fac Sci, CH-1015 Lausanne, Switzerland
关键词
halogen-metal permutation; metalation; protecting groups; regioflexibility; synthesis planning;
D O I
10.1002/anie.200300645
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This Review describes a concept aimed at rational and maximal structure proliferation. To this end, simple aromatic or heterocyclic starting materials, often bulk chemicals, are converted into all regionisomerically possible polar organometallic intermediates (mostly lithiated species), which then may be combined with any of the countless electrophiles to provide attractive new building blocks, particularly functionalized derivatives. The practical implementation relies on a set (toolbox") of sophisticated recipes developed by mechanistically guided modification of the two most prominent exchange methods used for the generation of polar organometallic compounds: hydrogen-metal and halogen-metal interconversion. These mutant methods ("old methods in a new outfit") amplify the existing options for organic synthesis by ensuring maximum regioflexibility. At the same time they offer new insight into factors that govern organometallic reactivity and provide hints on how to alter or finetune this reactivity judiciously."
引用
收藏
页码:376 / 393
页数:18
相关论文
共 125 条
[1]  
[Anonymous], 1994, PROG HETEROCYCL CHEM
[2]   First total synthesis of cryptomisrine [J].
Arzel, E ;
Rocca, P ;
Marsais, F ;
Godard, A ;
Quéguiner, G .
TETRAHEDRON, 1999, 55 (41) :12149-12156
[3]   The rate retarding effect of alkyl groups on arene metalation quantified [J].
Baston, E ;
Wang, Q ;
Schlosser, M .
TETRAHEDRON LETTERS, 2000, 41 (05) :667-670
[4]   ADDITIVITY OF ELECTRICAL EFFECTS IN AROMATIC ELECTROPHILIC SUBSTITUTIONS AS DETERMINED BY DESILYLATION REACTIONS [J].
BENKESER, RA ;
HICKNER, RA ;
HOKE, DI ;
THOMAS, OH .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1958, 80 (19) :5289-5294
[5]   DIRECTED LITHIATION OF UNPROTECTED BENZOIC-ACIDS [J].
BENNETAU, B ;
MORTIER, J ;
MOYROUD, J ;
GUESNET, JL .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1995, (10) :1265-1271
[6]  
Bobbio C, 2001, EUR J ORG CHEM, V2001, P4533
[7]  
BOBBIO C, 2003, UNPUB
[8]   SELECTIVE ORTHO LITHIATION OF (2,5-DIMETHOXYPHENYL)DIPHENYLPHOSPHINE OXIDE AND TRAPPING OF THE RESULTING ARYLLITHIUM WITH ELECTROPHILES [J].
BROWN, JM ;
WOODWARD, S .
JOURNAL OF ORGANIC CHEMISTRY, 1991, 56 (24) :6803-6809
[9]   BASE-CATALYZED HALOGEN DANCE, AND OTHER REACTIONS OF ARYL HALIDES [J].
BUNNETT, JF .
ACCOUNTS OF CHEMICAL RESEARCH, 1972, 5 (04) :139-&
[10]   Regiochemical observations on the lithiation of 1,2,4-trichlorobenzene and reaction with DMF and oxamide electrophiles in THF [J].
Burton, AJ ;
Cardwell, KS ;
Fuchter, MJ ;
Lindvall, MK ;
Patel, R ;
Packham, TW ;
Prodger, JC ;
Schilling, MB ;
Walker, MD .
TETRAHEDRON LETTERS, 2003, 44 (30) :5653-5656