Montmorillonite K10 clay-catalyzed synthesis of substituted 1-aryl indenes from Baylis-Hillman adducts

被引：44

作者：

Shanmugam, P ^{[1
]}

Rajasingh, P ^{[1
]}

机构：

[1] CSIR, Reg Res Lab, Div Organ Chem, Trivandrum 695019, Kerala, India

来源：

CHEMISTRY LETTERS | 2005年 / 34卷 / 11期

关键词：

D O I：

10.1246/cl.2005.1494

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

An eco-friend method for the synthesis of 1-aryl indenes from Baylis-Hillman adducts using Mont. K10 and microwave combination as catalyst system and a procedure for the synthesis of beta- phenyl-substituted-protected Baylis-Hillman adducts with highly Z-selectivity have been reported.

引用

页码：1494 / 1495

页数：2

共 50 条

[1] The first successful intermolecular Heck reaction of Baylis-Hillman adducts:: synthesis of β-aryl substituted Baylis-Hillman adducts
Kim, Jeong Mi
Kim, Ko Hoon
Kim, Taek Hyeon
Kim, Jae Nyoung
TETRAHEDRON LETTERS, 2008, 49 (20) : 3248 - 3251
[2] Montmorillonite K10 clay catalyzed mild, clean, solvent free one-pot protection-isomerisation of the Baylis-Hillman adducts with alcohols
Shanmugam, P
Rajasingh, P
CHEMISTRY LETTERS, 2002, (12) : 1212 - 1213
[3] Montmorillonite K10 clay-microwave assisted isomerisation of acetates of the Baylis-Hillman adducts:: A facile method of stereoselective synthesis of (E)-trisubstituted alkenes
Shanmugam, P
Singh, PR
SYNLETT, 2001, (08) : 1314 - 1316
[4] Montmorillonite K10 clay-catalyzed synthesis of silicon-tethered molecules
Dintzner, Matthew R.
Brown, Nathan D.
Brasovan, Kara
Zuziak, Matthew M.
ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2012, 243
[5] CHED 553-Montmorillonite K10 clay-catalyzed synthesis of phenazines
Pacilli, Massimo
Pileggi, Dominic J.
Dintzner, Matthew R.
ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2008, 235
[6] Montmorillonite K10 clay-catalyzed addition and cyclization reactions of aldehydes
Dintzner, Matthew R.
Little, Andrew J.
Pacilli, Massimo
Pileggi, Dominic J.
ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2007, 233
[7] Synthesis of substituted uracil derivatives from the acetates of the Baylis-Hillman adducts
Lee, CG
Gowrisankar, S
Kim, JN
BULLETIN OF THE KOREAN CHEMICAL SOCIETY, 2005, 26 (03) : 481 - 484
[8] Synthesis of poly-substituted pyrroles starting from the Baylis-Hillman adducts
Lee, Hyun Seung
Kim, Jeong Mi
Kim, Jae Nyoung
TETRAHEDRON LETTERS, 2007, 48 (23) : 4119 - 4122
[9] An expedient synthesis of 2-substituted naphthalenes from the Baylis-Hillman adducts
Kim, JN
Im, YJ
Gong, JH
Lee, KY
TETRAHEDRON LETTERS, 2001, 42 (25) : 4195 - 4197
[10] An expeditious synthesis of substituted pyrrolidines and tetrahydrofurans starting from baylis-hillman adducts
Gowrisankar, Saravanan
Kim, Hoo Sook
Lee, Hyun Seung
Kim, Jae Nyoung
BULLETIN OF THE KOREAN CHEMICAL SOCIETY, 2007, 28 (10): : 1844 - 1846

← 1 2 3 4 5 →