A new synthetic approach to phenol derivatives: Use of ring-closing olefin metathesis

被引:57
作者
Yoshida, K [1 ]
Imamoto, T [1 ]
机构
[1] Chiba Univ, Fac Sci, Dept Chem, Inage Ku, Chiba 2638522, Japan
关键词
D O I
10.1021/ja050853x
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Phenol derivatives, which are one of the most important classes of aromatic compounds in organic chemistry, were synthesized by ruthenium-catalyzed ring-closing olefin metathesis (RCM) of 1,4,7-trien-3-ones with versatile substitution patterns. The RCM reaction for producing phenol derivatives was also successful with 1,5,7-trien-3-one as another precursor. Most of the phenols prepared here could not be obtained easily by conventional methods. Copyright © 2005 American Chemical Society.
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页码:10470 / 10471
页数:2
相关论文
共 26 条
[1]   Synthesis of substituted 1,2-dihydroquinolines and quinolines using ene-ene metathesis and ene-enol ether metathesis [J].
Arisawa, M ;
Theeraladanon, C ;
Nishida, A ;
Nakagawa, M .
TETRAHEDRON LETTERS, 2001, 42 (45) :8029-8033
[2]  
BACKVALL JE, 1995, ORGANOMETALLICS, V14, P4242
[3]   Reaction between ruthenium(0) complexes and dihalo compounds. A new method for the synthesis of ruthenium olefin metathesis catalysts [J].
Belderrain, TR ;
Grubbs, RH .
ORGANOMETALLICS, 1997, 16 (18) :4001-4003
[4]   A general model for selectivity in olefin cross metathesis [J].
Chatterjee, AK ;
Choi, TL ;
Sanders, DP ;
Grubbs, RH .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (37) :11360-11370
[5]  
Chatterjee AK, 2002, ANGEW CHEM INT EDIT, V41, P3171, DOI 10.1002/1521-3773(20020902)41:17<3171::AID-ANIE3171>3.0.CO
[6]  
2-O
[7]   Recent developments in olefin cross-metathesis [J].
Connon, SJ ;
Blechert, S .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2003, 42 (17) :1900-1923
[8]   Sequential and cascade palladium catalysed cyclisation-anion capture-olefin metathesis [J].
Evans, P ;
Grigg, R ;
Ramzan, MI ;
Sridharan, V ;
York, M .
TETRAHEDRON LETTERS, 1999, 40 (15) :3021-3024
[9]  
Fürstner A, 2000, ANGEW CHEM INT EDIT, V39, P3012
[10]  
Grotjahn D. B, 1995, COMPREHENSIVE ORGANO, V12, P741