Facile access to optically active ferrocenyl derivatives with direct substitution of the hydroxy group catalyzed by indium tribromide

被引:84
作者
Vicennati, Paola [1 ]
Cozzi, Pier Giorgio [1 ]
机构
[1] Univ Bologna, Dipartimento Chim G Ciamician, I-40126 Bologna, Italy
关键词
ferrocene; alcohols; indium; tribromide; catalysis;
D O I
10.1002/ejoc.200700146
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Ferrocene derivatives have found many different uses and applications in organometallic chemistry, material chemistry, and catalysis. We have shown that using a catalytic amount (5-10 mol-%) of commercially available indium tribromide, at room temperature, many carbon nucleophiles, such as indoles, allylsilane, enolsilane, silyl ketene acetal, diketone, and trimethylsilylcyanide, smoothly react with different optically active ferrocenyl alcohol derivatives to afford the desired products in high yield, with retention of configuration. Also, many different N-nucleophiles (azide, carbamates) and O-nucleophiles (alcohols) react as well, again with retention of configuration. ((C) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007).
引用
收藏
页码:2248 / 2253
页数:6
相关论文
共 53 条
[1]   The synthesis of N,O-ferrocenyl pyrrolidine-containing ligands and their application in the diethyl- and diphenylzinc addition to aromatic aldehydes [J].
Ahern, Theresa ;
Muller-Bunz, Helge ;
Guiry, Patrick J. .
JOURNAL OF ORGANIC CHEMISTRY, 2006, 71 (20) :7596-7602
[2]   Recent applications of chiral ferrocene ligands in asymmetric catalysis [J].
Arrayas, Ramon Gomez ;
Adrio, Javier ;
Carretero, Juan Carlos .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2006, 45 (46) :7674-7715
[3]   The syntheses and catalytic applications of unsymmetrical ferrocene ligands [J].
Atkinson, RCJ ;
Gibson, VC ;
Long, NJ .
CHEMICAL SOCIETY REVIEWS, 2004, 33 (05) :313-328
[4]   A NEW CHIRAL TRIDENTATE FERROCENYL LIGAND - SYNTHESIS AND CHARACTERIZATION OF ITS PALLADIUM(II) AND NICKEL(II) COMPLEXES [J].
BARBARO, P ;
TOGNI, A .
ORGANOMETALLICS, 1995, 14 (07) :3570-3573
[5]   Phosphinoferrocenylaminophosphines as novel and practical ligands for asymmetric catalysis [J].
Boaz, NW ;
Debenham, SD ;
Mackenzie, EB ;
Large, SE .
ORGANIC LETTERS, 2002, 4 (14) :2421-2424
[6]   A concise update on the applications of chiral ferrocenyl phosphines in homogeneous catalysis leading to organic synthesis [J].
Colacot, TJ .
CHEMICAL REVIEWS, 2003, 103 (08) :3101-3118
[7]   HIGHLY ENANTIOSELECTIVE BORANE REDUCTION OF KETONES CATALYZED BY CHIRAL OXAZABOROLIDINES - MECHANISM AND SYNTHETIC IMPLICATIONS [J].
COREY, EJ ;
BAKSHI, RK ;
SHIBATA, S .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1987, 109 (18) :5551-5553
[8]   Nitrogen-containing ligands for asymmetric homogeneous and heterogeneous catalysis [J].
Fache, F ;
Schulz, E ;
Tommasino, ML ;
Lemaire, M .
CHEMICAL REVIEWS, 2000, 100 (06) :2159-2231
[9]   Gold(III)-catalyzed nucleophilic substitution of propargylic alcohols [J].
Georgy, M ;
Boucard, V ;
Campagne, JM .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (41) :14180-14181
[10]  
GOKEL GW, 1972, J ORG CHEM, V37, P3052, DOI 10.1021/jo00985a002