Grubbs' Ruthenium-Carbenes Beyond the Metathesis Reaction: Less Conventional Non-Metathetic Utility

被引:284
作者
Alcaide, Benito [1 ]
Almendros, Pedro [2 ]
Luna, Amparo [1 ]
机构
[1] Univ Complutense Madrid, Fac Quim, Dept Quim Organ 1, E-28040 Madrid, Spain
[2] CSIC, Inst Quim Organ Gen, E-28006 Madrid, Spain
关键词
RING-CLOSING METATHESIS; ALLYL PROTECTING GROUP; IN-SITU CONVERSION; OLEFIN-METATHESIS; CROSS-METATHESIS; ENYNE METATHESIS; TANDEM CATALYSIS; RUO4-CATALYZED KETOHYDROXYLATION; ASYMMETRIC-SYNTHESIS; TERMINAL ALKYNES;
D O I
10.1021/cr9001512
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Robert H. Grubbs has developed powerful new catalysts, which is stable in air, for metathesis that enabled custom synthesis of many new molecules. The widely used Grubbs' ruthenium carbene Ru-1, well-known for its ability to promote olefin metathesis, is also an effective catalyst in radical atom transfer reactions such as Kharasch addition. Bicyclic ring systems can be prepared from acyclic dienes through a tandem RCM-intramolecular Kharasch addition reaction sequence. Studies in the group of Quayle have revealed that there is an important rate difference between olefin metathesis and Kharasch reactions in substrates exposed to both reactions conditions. This group suggested that the process requires either direct denaturation of complex Ru-1, which is itself formed as a byproduct of the initial metathesis cycle, or generation of a new ruthenium complex. New uses of the ruthenium-based catalyst are likely, and contribute to its relevance as a versatile and effective tool in organic and organometallic chemistry.
引用
收藏
页码:3817 / 3858
页数:42
相关论文
共 176 条
[21]   Stereoselective synthesis of meso- and cis-2,6-diarylpiperidin-4-ones catalyzed by L-proline [J].
Aznar, Fernando ;
Garcia, Ana-Belen ;
Quinones, Noelia ;
Cabal, Maria-Paz .
SYNTHESIS-STUTTGART, 2008, 3 (03) :479-484
[22]   Proline-catalyzed imino-Diels-Alder reactions:: Synthesis of meso-2,6-diaryl-4-piperidones [J].
Aznar, Fernando ;
Garcia, Ana-Belen ;
Cabal, Maria-Paz .
ADVANCED SYNTHESIS & CATALYSIS, 2006, 348 (16-17) :2443-2448
[23]   A stereodivergent synthesis of virantmycin by an enzyme-mediated diester desymmetrization and a highly hindered aryl amination [J].
Back, TG ;
Wulff, JE .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2004, 43 (47) :6493-6496
[24]   Asymmetric total synthesis and X-ray crystal structure of the cytotoxic marine diterpene (+)-vigulariol [J].
Becker, Jochen ;
Bergander, Klaus ;
Froehlich, Roland ;
Hoppe, Dieter .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2008, 47 (09) :1654-1657
[25]   Sequential catalysis: A metathesis/dihydroxylation sequence [J].
Beligny, S ;
Eibauer, S ;
Maechling, S ;
Blechert, S .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2006, 45 (12) :1900-1903
[26]   A synthetic entry to 2,3-fused ring indole derivatives by ring-closing metathesis reactions [J].
Bennasar, ML ;
Zulaica, E ;
Tummers, S .
TETRAHEDRON LETTERS, 2004, 45 (33) :6283-6285
[27]   A concise synthesis of (-)-centrolobine via a diastereoselective ring rearrangement metathesis-isomerisation sequence [J].
Böhrsch, V ;
Blechert, S .
CHEMICAL COMMUNICATIONS, 2006, (18) :1968-1970
[28]   Tandem ring-closing metathesis and hydrogenation towards cyclic dinucleotides [J].
Borsting, P ;
Nielsen, P .
CHEMICAL COMMUNICATIONS, 2002, (18) :2140-2141
[29]   The Cl2(PCy3)(IMes)Ru(=CHPh) catalyst:: olefin metathesis versus olefin isomerization [J].
Bourgeois, D ;
Pancrazi, A ;
Nolan, SP ;
Prunet, J .
JOURNAL OF ORGANOMETALLIC CHEMISTRY, 2002, 643 :247-252
[30]   Substituent effects in tandem ring-closing metathesis reactions of dienynes [J].
Boyer, FD ;
Hanna, I .
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2006, 2006 (02) :471-482