O-DPPB-Directed copper-mediated allylic substitution: Part 3. Stereospecific and stereodivergent construction of tertiary and quaternary carbon centers through switchable directed/nondirected allylic substitution

被引:39
作者
Breit, Bernhard
Demel, Peter
Grauer, Daniel
Studte, Christopher
机构
[1] Univ Freiburg, Inst Organ Chem & Biochem, D-79104 Freiburg, Germany
[2] Boehringer Ingelheim Austria GmbH, Med Chem, A-1121 Vienna, Austria
关键词
allylation; asymmetric synthesis; Grignard reagents; organocopper reagents; stereoselectivity;
D O I
10.1002/asia.200600100
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This study introduces the ortho-diphenylphosphanylbenzoate (o-DPPB)/o-DPPB oxide system as a switchable directing/nondirecting leaving group in a copper-mediated allylic substitution with Grignard and organozinc reagents. With this system, the regioselective, stereospecific, and stereodivergent construction of quaternary as well as tertiary carbon centers is possible in a reliable and predictable fashion. Starting from one substrate enantiomer, both optical antipodes of the substitution products are readily available. Hence, this methodology features reversed polarity in comparison to established enolate alkylation chemistry and may be an interesting alternative, particularly for the construction of quaternary stereogenic carbon centers.
引用
收藏
页码:586 / 597
页数:12
相关论文
共 70 条
[1]  
[Anonymous], 2003, ANGEW CHEM
[2]   Direct, stereoselective substitution in [Rh(CO)2CI]2-catalyzed allylic alkylations of unsymmetrical substrates [J].
Ashfeld, BL ;
Miller, KA ;
Martin, SF .
ORGANIC LETTERS, 2004, 6 (08) :1321-1324
[3]   OXIDATION OF ALPHA,BETA-UNSATURATED ALDEHYDES [J].
BAL, BS ;
CHILDERS, WE ;
PINNICK, HW .
TETRAHEDRON, 1981, 37 (11) :2091-2096
[4]   SUBSTITUTION OF ALLYLIC SULFIDES OF BENZOTHIAZOLE-2-THIOL WITH ORGANOMAGNESIUM COMPOUNDS IN THE PRESENCE OF COPPER(I) IODIDE - REGIOSELECTIVE SYNTHESIS OF OLEFINS [J].
BARSANTI, P ;
CALO, V ;
LOPEZ, L ;
MARCHESE, G ;
NASO, F ;
PESCE, G .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1978, (24) :1085-1086
[5]  
Boeckman R.K., 2000, J ORG SYN, V77, P141, DOI 10.15227/orgsyn.077.0141
[6]   Enantioselective copper-mediated allylic substitution with Grignard reagents employing a chiral reagent-directing leaving group [J].
Breit, B ;
Breuninger, D .
SYNTHESIS-STUTTGART, 2005, (01) :147-157
[7]   Stereospecific and stereodivergent construction of quaternary carbon centers through switchable directed/nondirected allylic substitution [J].
Breit, B ;
Demel, P ;
Studte, C .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2004, 43 (29) :3786-3789
[8]   Iterative deoxypropionate synthesis based on a copper-mediated directed allylic substitution [J].
Breit, B ;
Herber, C .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2004, 43 (29) :3790-3792
[9]   Hydrogen bonding as a construction element for bidentate donor ligands in homogeneous catalysis: Regioselective hydroformylation of terminal alkenes [J].
Breit, B ;
Seiche, W .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (22) :6608-6609
[10]  
Breit B, 2002, MODERN ORGANOCOPPER CHEMISTRY, P188, DOI 10.1002/3527600086.ch6