Montmorillonite K-10: As a Useful Catalyst in Organic Preparations

被引:12
作者
Baghernejad, Bita [1 ]
机构
[1] PNU, Sch Sci, Dept Chem, Tehran, Iran
关键词
Montmorillonite K-10; heterogenous catalysis; organic reactions; reusable; modified; transformation; FRIEDEL-CRAFTS ALKYLATION; OXIDATIVE DEPROTECTION; SOLID-STATE; TETRAHYDROPYRANYL ETHERS; QUINOXALINE DERIVATIVES; AMMONIUM CHLOROCHROMATE; ENVIRONMENTALLY BENIGN; EFFICIENT SYNTHESIS; HIGHLY EFFICIENT; CLAY CATALYSIS;
D O I
10.2174/157017810791112487
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Montmorillonite K-10 has been used in many organic preparations as a good solid catalyst. In this review, we wish to report some applications of this catalyst in organic reactions.
引用
收藏
页码:255 / 268
页数:14
相关论文
共 96 条
[41]   Friedel-Crafts alkylation of a cage enone:: synthesis of aralkyl substituted tetracyclo[5.3.1.0[2,6].0[4,8]]undeca-9,11-diones and the formation of fascinating novel cage compounds with pyrrole and thiophene using Montmorillonite K-10 [J].
James, Beena ;
Suresh, E. ;
Nair, Mangalam S. .
TETRAHEDRON LETTERS, 2007, 48 (34) :6059-6063
[42]   Synthesis of new quinoxaline-2-carboxylate 1,4-dioxide derivatives as anti-Mycobacterium tuberculosis agents [J].
Jaso, A ;
Zarranz, B ;
Aldana, I ;
Monge, A .
JOURNAL OF MEDICINAL CHEMISTRY, 2005, 48 (06) :2019-2025
[43]   Efficient and convenient procedure for preparation of N-sulfonylimines catalyzed by montmorillonite K-10 [J].
Jin, Tong-Shou ;
Yu, Mi-Jun ;
Liu, Li-Bin ;
Zhao, Ying ;
Li, Tong-Shuang .
SYNTHETIC COMMUNICATIONS, 2006, 36 (16) :2339-2344
[44]   Transesterification of β-ketoesters with alcohols catalyzed by montmorillonite K-10 [J].
Jin, TS ;
Zhang, SL ;
Li, TS .
GREEN CHEMISTRY, 2002, 4 (01) :32-34
[45]   Montmorillonite K 10-catalyzed regioselective addition of thiols and thiobenzoic acids onto olefins: an efficient synthesis of dithiocarboxylic esters [J].
Kanagasabapathy, S ;
Sudalai, A ;
Benicewicz, BC .
TETRAHEDRON LETTERS, 2001, 42 (23) :3791-3794
[46]   Montmorillonite K10 catalyzed efficient synthesis of arnidoalkyl naphthols under solvent free conditions [J].
Kantevari, Srinivas ;
Vuppalapati, Srinivasu V. N. ;
Nagarapu, Lingaiah .
CATALYSIS COMMUNICATIONS, 2007, 8 (11) :1857-1862
[47]  
Karade NN, 2003, J CHEM RES, P652
[48]   Facile synthesis of 1,1-diacetates from aldehydes using montmorillonite K-10 clay under microwave irradiation [J].
Karmakar, D ;
Prajapati, D ;
Sandhu, JS .
JOURNAL OF CHEMICAL RESEARCH-S, 1998, (07) :382-+
[49]   Synthesis of quinoxaline derivatives bearing the styryl and phenylethynyl groups and application to a fluorescence derivatization reagent [J].
Katoh, A ;
Yoshida, T ;
Ohkanda, J .
HETEROCYCLES, 2000, 52 (02) :911-920
[50]   A novel and highly efficient method for the direct conversion of aryl aldehyde bisulfite adducts to their aryl trimethylsilyl ethers in a one-pot manner catalyzed by montmorillonite K-10 [J].
Khodaei, MM ;
Khosropour, AR ;
Abbasi, J .
PHOSPHORUS SULFUR AND SILICON AND THE RELATED ELEMENTS, 2006, 181 (01) :93-97