Literature DB >> 12636368

Bismuth nitrate-catalyzed versatile Michael reactions.

Neeta Srivastava1, Bimal K Banik.   

Abstract

Bismuth nitrate-catalyzed versatile Michael reaction was developed to reduce the complications that characterize the current standard Michael reaction and used for facile preparation of organic compounds of widely different structures. For example, several substituted amines, imidazoles, thio compounds, indoles, and carbamates were prepared at room temperature by following this method. In contrast with the existing methods using many acidic catalysts, this method is very general, simple, high-yielding, environmentally friendly, and oxygen and moisture tolerant. However, the promoting role of bismuth nitrate in this reaction is not understood at this time.

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Year:  2003        PMID: 12636368     DOI: 10.1021/jo026550s

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  12 in total

1.  The Michael addition of indoles and pyrrole to alpha-, beta-unsaturated ketones and double-conjugate 1,4-addition of indoles to symmetric enones promoted by pulverization-activation method and Thia-Michael addition catalyzed by wet cyanuric chloride.

Authors:  Ramin Ghorbani-Vaghei; Hojat Veisi
Journal:  Mol Divers       Date:  2009-08-07       Impact factor: 2.943

2.  Bismuth nitrate pentahydrate-induced novel nitration of eugenol.

Authors:  Luis Canales; Debasish Bandyopadhyay; Bimal K Banik
Journal:  Org Med Chem Lett       Date:  2011-09-20

3.  Bismuth nitrate-induced microwave-assisted expeditious synthesis of vanillin from curcumin.

Authors:  Debasish Bandyopadhyay; Bimal K Banik
Journal:  Org Med Chem Lett       Date:  2012-04-20

4.  Tetrabutylammonium bromide media aza-Michael addition of 1,2,3,6-tetrahydrophthalimide to symmetrical fumaric esters and acrylic esters under solvent-free conditions.

Authors:  Gholamhassan Imanzadeh; Farzaneh Ahmadi; Mohammadreza Zamanloo; Yagoub Mansoori
Journal:  Molecules       Date:  2010-10-21       Impact factor: 4.411

5.  An efficient synthesis of 1-aryl-3-(indole-3-yl)-3-(2-aryl-1,2,3-triazol-4-yl)propan-1-one catalyzed by a Brønsted acid ionic liquid.

Authors:  Chen-Jiang Liu; Chuan-Ji Yu
Journal:  Molecules       Date:  2010-12-10       Impact factor: 4.411

6.  A microwave-assisted bismuth nitrate-catalyzed unique route toward 1,4-dihydropyridines.

Authors:  Debasish Bandyopadhyay; Stephanie Maldonado; Bimal K Banik
Journal:  Molecules       Date:  2012-03-05       Impact factor: 4.411

7.  A highly efficient bismuth salts-catalyzed route for the synthesis of α-aminophosphonates.

Authors:  Antara Banik; Sahil Batta; Debasish Bandyopadhyay; Bimal K Banik
Journal:  Molecules       Date:  2010-11-12       Impact factor: 4.411

8.  Remarkable iodine-catalyzed synthesis of novel pyrrole-bearing N-polyaromatic beta-lactams.

Authors:  Debasish Bandyopadhyay; Gildardo Rivera; Isabel Salinas; Hector Aguilar; Bimal K Banik
Journal:  Molecules       Date:  2010-02-23       Impact factor: 4.411

9.  Silica sulfuric acid promotes aza-Michael addition reactions under solvent-free condition as a heterogeneous and reusable catalyst.

Authors:  Yan Wang; Yan-Qin Yuan; Sheng-Rong Guo
Journal:  Molecules       Date:  2009-11-23       Impact factor: 4.411

10.  Conjugate addition of indoles to alpha,beta-unsaturated ketones using a Brønsted acid ionic liquid as an efficient catalyst.

Authors:  Chuan-Ji Yu; Chen-Jiang Liu
Journal:  Molecules       Date:  2009-08-27       Impact factor: 4.411

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