Main Article Content
Abstract
Microwave-induced synthesis of bis-β-lactams is performed by Staudinger cycloaddition reaction of acid chloride and hydrobenzamide.
Keywords
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References
- B.K. Banik, Heterocyclic Scaffolds I, Topics in Heterocyclic Chemistry, Springer, vol. 22, pp. 1-379 (2010).
- B.K. Banik, b-Lactams: Synthesis and Biological Evaluation, In: Topics in Heterocyclic Chemistry, Springer, vol. 30, pp. 1-226 (2012).
- B.K. Banik, b-Lactam Chemistry, Tetrahedron Symposium-in-Print, 68, 10627 (2012); https://doi.org/10.1016/S0040-4020(12)01701-2.
- I. Banik and B.K. Banik, Microwave-Induced Chemical Manipulation of b-Lactam, Springer, vol. 88, pp. 781-1007 (2012).
- B.K. Banik, Beta Lactams: Novel Synthetic Pathways and Applications, Springer, pp. 1-419 (2017).
- P.T. Parvatkar, P.S. Parameswaran and B.K. Banik, ed.: B.K. Banik, Solid Phase Synthesis of b-Lactams: Results and Scope, In: Beta Lactams: Novel Synthetic Pathways and Applications, Springer, pp. 253-284 (2017).
- S. Basu and B.K. Banik, ed.: B.K. Banik, Beta Lactams as Clinically Active Molecules, In: Beta Lactams: Novel Synthetic Pathways and Applications, Springer, pp. 285-310 (2017).
- B.K. Banik, Synthesis and Biological Studies of Novel b-Lactams, CRC Book, pp. 31-72 (2013).
- B.K. Banik, K.J. Barakat, D.R. Wagle, M.S. Manhas and A.K. Bose, Microwave-Assisted Rapid and Simplified Hydrogenation, J. Org. Chem., 64, 5746 (1999); https://doi.org/10.1021/jo981516s.
- B.K. Banik, H. Aguilar and D. Cordova, Unprecedented Stereocontrol of b-Lactam Formation Derived from N-Cinnamylidenearylamine, Heterocycles, 71, 2321 (2007); https://doi.org/10.3987/COM-07-11134.
- A. Kall, D. Bandyopadhyay and B.K. Banik, Microwave-Induced Aza-Michael Reaction in Water: A Remarkably Simple Procedure, Synth. Commun., 40, 1730 (2010); https://doi.org/10.1080/00397910903134634.
- K. Ramos and B.K. Banik, Microwave-Induced Clay-Mediated Preparation of Imines: One-Pot Synthesis of b-Lactams, Heterocycl. Lett., 1, 27 (2011).
- I. Banik, S. Samajdar and B.K. Banik, Microwave-Induced Stereo-specific Synthesis of b-Lactams Derived from Polyaromatic Imines: Influence of Multicyclic Rings at the Nitrogen, Heterocycl. Lett., 1, 55 (2011).
- D. Bandyopadhyay, M.A. Yanez and B.K. Banik, Microwave-Induced Stereoselectivity of b-Lactam Formation, Effects of Solvents; Heterocycl. Lett., 1, 65 (2011).
- D. Bandyopadhyay, S. Mukherjee and B.K. Banik, An Expeditious Synthesis of N-substituted Pyrroles via Microwave-Induced Iodine-Catalyzed Reactions under Solventless Conditions, Molecules, 15, 2520 (2010); https://doi.org/10.3390/molecules15042520.
- D. Bandyopadhyay, S. Mukherjee, R. Rodriguez and B.K. Banik, An Effective Microwave-Induced Iodine-Catalyzed Method for the Synthesis of Quinoxalines via Condensation of 1,2-Diamines with 1,2-Dicarbonyl Compounds, Molecules, 15, 4207 (2010); https://doi.org/10.3390/molecules15064207.
- D. Bandyopadhyay, J. Cruz and B.K. Banik, Novel Synthesis of 3-Pyrrole Substituted b-Lactams via Microwave-Induced Bismuth Nitrate-Catalyzed Reaction, Tetrahedron, 68, 10686 (2012); https://doi.org/10.1016/j.tet.2012.06.009.
- S.H. Park, S.Y. Lee and A.K. Bose, An Efficient and Eco-friendly Approach to 15N-Unsubstituted b-Lactams: 15N-Labled Synthons for Taxol and Its Analoss, Bull. Korean Chem. Soc., 22, 493 (2001).
- A.K. Bose, B.K. Banik and M.S. Manhas, Stereocontrol of b-Lactam formation Using Microwave Irradiation, Tetrahedron Lett., 36, 213 (1995); https://doi.org/10.1016/0040-4039(94)02225-Z.
- H. Aguilar and B.K. Banik, Stereoselectivity of 3,3-Disubstituted b-Lactam Formation via Staudinger Reaction, Heterocycl. Commun., 15, 365 (2009); https://doi.org/10.1515/HC.2009.15.5.365.
- D. Bandyopadhyay and B.K. Banik, Microwave-Induced Stereocontrol of b-Lactam Formation with an N-Benzylidene-9,10-dihydrophenan-thren-3-amine via Staudinger Cycloaddition, Helv. Chim. Acta, 93, 298 (2010); https://doi.org/10.1002/hlca.200900212.
- R. Rodriguez and B.K. Banik, Unprecedented Stereoselectivity of b-Lactam Formation via Staudinger Reaction with Conjugated Imines Derived from Polyaromatic Systems, Heterocycl. Lett., 1, 31 (2011).
References
B.K. Banik, Heterocyclic Scaffolds I, Topics in Heterocyclic Chemistry, Springer, vol. 22, pp. 1-379 (2010).
B.K. Banik, b-Lactams: Synthesis and Biological Evaluation, In: Topics in Heterocyclic Chemistry, Springer, vol. 30, pp. 1-226 (2012).
B.K. Banik, b-Lactam Chemistry, Tetrahedron Symposium-in-Print, 68, 10627 (2012); https://doi.org/10.1016/S0040-4020(12)01701-2.
I. Banik and B.K. Banik, Microwave-Induced Chemical Manipulation of b-Lactam, Springer, vol. 88, pp. 781-1007 (2012).
B.K. Banik, Beta Lactams: Novel Synthetic Pathways and Applications, Springer, pp. 1-419 (2017).
P.T. Parvatkar, P.S. Parameswaran and B.K. Banik, ed.: B.K. Banik, Solid Phase Synthesis of b-Lactams: Results and Scope, In: Beta Lactams: Novel Synthetic Pathways and Applications, Springer, pp. 253-284 (2017).
S. Basu and B.K. Banik, ed.: B.K. Banik, Beta Lactams as Clinically Active Molecules, In: Beta Lactams: Novel Synthetic Pathways and Applications, Springer, pp. 285-310 (2017).
B.K. Banik, Synthesis and Biological Studies of Novel b-Lactams, CRC Book, pp. 31-72 (2013).
B.K. Banik, K.J. Barakat, D.R. Wagle, M.S. Manhas and A.K. Bose, Microwave-Assisted Rapid and Simplified Hydrogenation, J. Org. Chem., 64, 5746 (1999); https://doi.org/10.1021/jo981516s.
B.K. Banik, H. Aguilar and D. Cordova, Unprecedented Stereocontrol of b-Lactam Formation Derived from N-Cinnamylidenearylamine, Heterocycles, 71, 2321 (2007); https://doi.org/10.3987/COM-07-11134.
A. Kall, D. Bandyopadhyay and B.K. Banik, Microwave-Induced Aza-Michael Reaction in Water: A Remarkably Simple Procedure, Synth. Commun., 40, 1730 (2010); https://doi.org/10.1080/00397910903134634.
K. Ramos and B.K. Banik, Microwave-Induced Clay-Mediated Preparation of Imines: One-Pot Synthesis of b-Lactams, Heterocycl. Lett., 1, 27 (2011).
I. Banik, S. Samajdar and B.K. Banik, Microwave-Induced Stereo-specific Synthesis of b-Lactams Derived from Polyaromatic Imines: Influence of Multicyclic Rings at the Nitrogen, Heterocycl. Lett., 1, 55 (2011).
D. Bandyopadhyay, M.A. Yanez and B.K. Banik, Microwave-Induced Stereoselectivity of b-Lactam Formation, Effects of Solvents; Heterocycl. Lett., 1, 65 (2011).
D. Bandyopadhyay, S. Mukherjee and B.K. Banik, An Expeditious Synthesis of N-substituted Pyrroles via Microwave-Induced Iodine-Catalyzed Reactions under Solventless Conditions, Molecules, 15, 2520 (2010); https://doi.org/10.3390/molecules15042520.
D. Bandyopadhyay, S. Mukherjee, R. Rodriguez and B.K. Banik, An Effective Microwave-Induced Iodine-Catalyzed Method for the Synthesis of Quinoxalines via Condensation of 1,2-Diamines with 1,2-Dicarbonyl Compounds, Molecules, 15, 4207 (2010); https://doi.org/10.3390/molecules15064207.
D. Bandyopadhyay, J. Cruz and B.K. Banik, Novel Synthesis of 3-Pyrrole Substituted b-Lactams via Microwave-Induced Bismuth Nitrate-Catalyzed Reaction, Tetrahedron, 68, 10686 (2012); https://doi.org/10.1016/j.tet.2012.06.009.
S.H. Park, S.Y. Lee and A.K. Bose, An Efficient and Eco-friendly Approach to 15N-Unsubstituted b-Lactams: 15N-Labled Synthons for Taxol and Its Analoss, Bull. Korean Chem. Soc., 22, 493 (2001).
A.K. Bose, B.K. Banik and M.S. Manhas, Stereocontrol of b-Lactam formation Using Microwave Irradiation, Tetrahedron Lett., 36, 213 (1995); https://doi.org/10.1016/0040-4039(94)02225-Z.
H. Aguilar and B.K. Banik, Stereoselectivity of 3,3-Disubstituted b-Lactam Formation via Staudinger Reaction, Heterocycl. Commun., 15, 365 (2009); https://doi.org/10.1515/HC.2009.15.5.365.
D. Bandyopadhyay and B.K. Banik, Microwave-Induced Stereocontrol of b-Lactam Formation with an N-Benzylidene-9,10-dihydrophenan-thren-3-amine via Staudinger Cycloaddition, Helv. Chim. Acta, 93, 298 (2010); https://doi.org/10.1002/hlca.200900212.
R. Rodriguez and B.K. Banik, Unprecedented Stereoselectivity of b-Lactam Formation via Staudinger Reaction with Conjugated Imines Derived from Polyaromatic Systems, Heterocycl. Lett., 1, 31 (2011).