Strategies for heterocyclic construction via novel multicomponent reactions based on isocyanides and nucleophilic carbenes
(a) Vijjay, N. C; Rajesh, A. U; Vinod, S; Bindu, A. R; Sreekanth, J. S; Lakshmi, B. Strategies for heterocyclic construction via novel multicomponent reactions based on isocyanides and nucleophilic carbenes. Acc. Chem. Res. 2003, 36, 899-907;.
An efficient method for the synthesis of benzo[f]quinoline and ben-zo[a]phenanthridine derivatives catalyzed by iodine by a three-component reaction of arene-carbaldehyde, naphthalen-2-amine, and cyclic ketone
(d) Wang, X. S; Li, Q; Yao, C. S; Tu, S. J. An efficient method for the synthesis of benzo[f]quinoline and ben-zo[a]phenanthridine derivatives catalyzed by iodine by a three-component reaction of arene-carbaldehyde, naphthalen-2-amine, and cyclic ketone. Eur. J. Org. Chem. 2008, 3513-3518;.
An aerobic ligandless palladium acetate-catalysed Suzuki-Miyaura cross-coupling reaction in an aqueous solvent
(e) Li, C; Li, X. Q; Zhang, C. An aerobic ligandless palladium acetate-catalysed Suzuki-Miyaura cross-coupling reaction in an aqueous solvent. J. Chem. Res. 2008, 525-527;.
Multi-component one-pot synthesis of the tumor-associated carbohydrate antigen globo-H based on preactivation of thioglycosyl donors
(a) Wang, Z; Zhou, L; El-Boubbou, K; Ye, X. S; Huang, X. Multi-component one-pot synthesis of the tumor-associated carbohydrate antigen globo-H based on preactivation of thioglycosyl donors. J. Org. Chem. 2007, 72, 6409-6420;.
A novel and facile synthesis of 2-(cyclohexylamino)-6,7-dihydro-3-aryl- 1H-indole-4(5H)-ones via a one-pot multi-component reaction
(b) Heravi, M. M; Baghernejad, B; Oskooie, H. A; Hekmatshoar, R. A novel and facile synthesis of 2-(cyclohexylamino)-6,7-dihydro-3-aryl-1H-indole-4(5H)- ones via a one-pot multi-component reaction. Tetrahedron Lett. 2008, 49, 6101-6103;.
Surface-mediated synthesis of unsymmetrical O,O-dialkyl alkyl pyrophosphonates using neutral alumina: Potential chemical weapons convention-related compounds
(c) Shinde, S. V; Jadhav, W. N; Kondre, J. M; Gampawar, V. N. S; Karade, N. Surface-mediated synthesis of unsymmetrical O,O-dialkyl alkyl pyrophosphonates using neutral alumina: Potential chemical weapons convention-related compounds. J. Chem. Res. 2008, 273-277;.
2 4,5-Trisubstituted thiazole building blocks by a novel multi-component reaction
(d) Umkehrer, M; Kolb, J; Burdack, C; Hiller, W. 2,4,5-Trisubstituted thiazole building blocks by a novel multi-component reaction. Synlett. 2005, 79-82.
One-pot clean synthesis of 1,8-doxo-decahydroacridines catalyzed by p-dodecylbenezenesulfonic acid in aqueous media
(a) Jin, T. S; Zhang, J. S; Guo, T. T; Wang, A. Q; Li, T. S. One-pot clean synthesis of 1,8-doxo-decahydroacridines catalyzed by p- dodecylbenezenesulfonic acid in aqueous media. Synthesis 2004, 2001-2005;.
Catalysis and regioselectivity of the aqueous Heck reaction by Pd(0) nanoparticles under ultrasonic irradiation
(c) Zhang, Z. H; Zha, Z. G; Gan, C. S; Pan, C. F; Zhou, Y. Q; Wang, Z. Y; Zhou, M. M. Catalysis and regioselectivity of the aqueous Heck reaction by Pd(0) nanoparticles under ultrasonic irradiation. J. Org. Chem. 2006, 71, 4339-4342;.
Three-component one-pot synthesis of unsymmetrical 1,4-dihydropyridine derivatives in aqueous media
(d) Shi, D. Q; Yu, C. X; Zhuang, Q. Y. Three-component one-pot synthesis of unsymmetrical 1,4-dihydropyridine derivatives in aqueous media. J. Chem. Res. 2008, 441-443;.
A simple and clean procedure for the synthesis of polyhydroacridine and quinoline derivatives: Reaction of Schiff base with 1,3-dicarbonyl compounds in aqueous medium
(a) Wang, X. S; Zhang, M. M; Zeng, Z. S; Shi, D. Q; Tu, S. J; Wei, X. Y; Zong, Z. M. A simple and clean procedure for the synthesis of polyhydroacridine and quinoline derivatives: Reaction of Schiff base with 1,3-dicarbonyl compounds in aqueous medium. Tetrahedron Lett. 2005, 46, 7169-7173;.
An unexpected ring-opening of 2-pyrone ring in the synthesis of 1-arylbenzo[f]quinoline-2-carboxmide derivatives in aqueous media catalyzed by TEBAC
(b) Wang, X. S; Zhang, M. M; Li, Q; Yao, C. S; Tu, S. J. An unexpected ring-opening of 2-pyrone ring in the synthesis of 1-arylbenzo[f]quinoline-2- carboxmide derivatives in aqueous media catalyzed by TEBAC. Synlett. 2007, 3141-3144;.
Unexpected spiro-benzoquinolines in the reaction of N-(arylidene) naphthalen-2-amine, arylaldehyde, and 1,3-dimethylbarbituric acid in water
(c) Wang, X. S; Zhang, M. M; Jiang, H; Li, Q; Shi, D. Q; Tu, S. J. Unexpected spiro-benzoquinolines in the reaction of N-(arylidene)naphthalen-2- amine, arylaldehyde, and 1,3-dimethylbarbituric acid in water. Chem. Lett. 2007, 36, 450-451;.
A new synthesis method for benzo[f]quinolin-3-carbonyl urea and thiourea derivatives in aqueous media catalyzed by TEBAC
(d) Wang, X. S; Zhang, M. M; Shi, D. Q; Tu, S. J; Wei, X. Y; Zong, Z. M. A new synthesis method for benzo[f]quinolin-3-carbonyl urea and thiourea derivatives in aqueous media catalyzed by TEBAC. J. Heterocycl. Chem. 2007, 36, 441-447;.