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
[21]   Synthesis of trisubstituted furans from 2-bromo-5-methylfuran via halogen migrations and their selective preventions [J].
Frohlich, J ;
Hametner, C .
MONATSHEFTE FUR CHEMIE, 1996, 127 (04) :435-443
[22]   Synthesis of trisubstituted thiophenes via a halogen dance reaction at 2-bromo-5-methylthiophene [J].
Frohlich, J ;
Hametner, C ;
Kalt, W .
MONATSHEFTE FUR CHEMIE, 1996, 127 (03) :325-330
[23]   Dibenzofuran. V. Dimetalation [J].
Gilman, H ;
Young, RV .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1935, 57 (01) :1121-1123
[24]   Secondary and tertiary alkyllithium compounds and some interconversion reactions with them [J].
Gilman, H ;
Moore, FW ;
Baine, O .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1941, 63 :2479-2482
[25]   Metalation as a side reaction in the preparation of organolithium compounds [J].
Gilman, H ;
Langham, W ;
Jacoby, AL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1939, 61 :106-109
[26]  
GINANNESCHI A, 2002, UNPUB
[27]   Selectivities in reactions of organolithium reagents with unprotected 2-halobenzoic acids [J].
Gohier, F ;
Castanet, AS ;
Mortier, J .
ORGANIC LETTERS, 2003, 5 (11) :1919-1922
[28]  
GOHIER F, 2003, THESIS U MAINE LE MA
[29]   Deprotonation-triggered heavy-halogen migrations as a key to the structural elaboration of 2,2-difluoro-1,3-benzodioxole [J].
Gorecka, J ;
Leroux, F ;
Schlosser, M .
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2004, 2004 (01) :64-68
[30]  
GORECKA J, IN PRESS ORG LETT