A Novel Asymmetric Synthesis of 3-(1 H-Pyrrol-1-yl)-Substituted β-Lactams via a Bismuth Nitrate-Catalyzed Reaction.
- Published in:
- Helvetica Chimica Acta, 2012, v. 95, n. 5, p. 839, doi. 10.1002/hlca.201100202
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- Article
Works matching AU Banik, Bimal K.
Results: 28
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An Efficient Synthesis of Optically Active trans-(3 R,4 R)-3-Acetoxy-4-aryl-1-(chrysen-6-yl)azetidin-2-ones Using (+)-Car-3-ene as a Chiral Auxiliary.
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- Helvetica Chimica Acta, 2011, v. 94, n. 12, p. 2188, doi. 10.1002/hlca.201100225
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- Article
3
Stereoselective synthesis of novel monocyclic trans -3-halogenated-4-pyrazolyl- β -lactams: Potential synthons and promising biologically active agents.
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- Synthetic Communications, 2017, v. 47, n. 23, p. 2239, doi. 10.1080/00397911.2017.1371759
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- Article
4
Diastereoselective synthesis of novel 3-aryloxy/alkoxy-4-benzothiazolylpyrazolyl- β -lactams: Potential synthons for novel aminoacids/nanocopolymers.
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- Synthetic Communications, 2017, v. 47, n. 21, p. 1955, doi. 10.1080/00397911.2017.1357186
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- Article
5
Synthetic route for the novel pyrimidine-substituted alkanoate, acetohydrazide, and imines: Synthon for β -lactams.
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- Synthetic Communications, 2017, v. 47, n. 10, p. 982, doi. 10.1080/00397911.2017.1301479
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- Publication type:
- Article
6
Potential Effects of Iodine Supplementation on Inflammatory Processes and Toxin Removal Following COVID-19 Vaccination.
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- Biological Trace Element Research, 2022, v. 200, n. 9, p. 3941, doi. 10.1007/s12011-021-02996-5
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- Article
7
Polysaccharides from Dolichos biflorus Linn and Trachyspermum ammi Linn seeds: isolation, characterization and remarkable antimicrobial activity.
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- Chemistry Central Journal, 2017, v. 11, p. 1, doi. 10.1186/s13065-017-0349-2
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- Article
8
On the Stereodivergent Behavior Observed in the Staudinger Reaction between Methoxyketene and ( E)- N-Benzylidenearyl Amines.
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- Angewandte Chemie International Edition, 2007, v. 46, n. 17, p. 3028, doi. 10.1002/anie.200605231
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- Article
9
Microwave-induced perchloric acid catalyzed novel solvent-free synthesis of 4-aryl-3,4-dihydropyrimidones via biginelli condensation.
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- Journal of Heterocyclic Chemistry, 2007, v. 44, n. 4, p. 979, doi. 10.1002/jhet.5570440439
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- Publication type:
- Article
10
Tellurium-induced functional group activation.
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- Physical Sciences Reviews, 2023, v. 8, n. 12, p. 4821, doi. 10.1515/psr-2021-0221
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- Article
11
Metal‐Free Cross‐Dehydrogenative Coupling (CDC): Molecular Iodine as a Versatile Catalyst/Reagent for CDC Reactions.
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- Chemistry - An Asian Journal, 2019, v. 14, n. 1, p. 6, doi. 10.1002/asia.201801237
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- Article
12
Synthesis of Bicyclo[3.2.1]-octanone Derivatives by Metal Catalyzed Decomposition of α-Diazomethylketones.
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- Synthetic Communications, 1997, v. 27, n. 20, p. 3637, doi. 10.1080/00397919708007087
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- Publication type:
- Article
13
Synthesis of (±)-2-Methoxy-9a-Carbamorphinan and (±)-2-Methoxy-9a-Carba-14α-Morphinan: Acid Catalyzed Cyclizations of 1- m -Methoxybenzyl-4, 4a,5,6,7,8-Hexahydronaphthalen-2(3H)-ONE and 1 - m -Methox Ybenzyloctalins.
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- Synthetic Communications, 1990, v. 20, n. 14, p. 2203, doi. 10.1080/00397919008053160
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- Publication type:
- Article
14
An Expeditious Total Synthesis of (±)-Sempervirol, (±)-Sugiol and (±)-Xanthopherol Methyl Ether by Acid-Catalyzed Cyclialkylation Route.
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- Synthetic Communications, 1989, v. 19, n. 7/8, p. 1351, doi. 10.1080/00397918908054545
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- Publication type:
- Article
15
An Expeditious Iodine-Catalyzed Synthesis of 3-Pyrrole-substituted 2-Azetidinones.
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- Molecules, 2012, v. 17, n. 10, p. 11570, doi. 10.3390/molecules171011570
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- Publication type:
- Article
16
A Microwave-Assisted Bismuth Nitrate-Catalyzed Unique Route Toward 1,4-Dihydropyridines.
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- Molecules, 2012, v. 17, n. 3, p. 2643, doi. 10.3390/molecules17032643
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- Publication type:
- Article
17
A Highly Efficient Bismuth Salts-Catalyzed Route for the Synthesis of α-Aminophosphonates.
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- Molecules, 2010, v. 15, n. 11, p. 8205, doi. 10.3390/molecules15118205
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- Publication type:
- Article
18
An Effective Microwave-Induced Iodine-Catalyzed Method for the Synthesis of Quinoxalines via Condensation of 1,2-Diamines with 1,2-Dicarbonyl Compounds.
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- Molecules, 2010, v. 15, n. 6, p. 4207, doi. 10.3390/molecules15064207
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- Publication type:
- Article
19
An Expeditious Synthesis of N-substituted Pyrroles via Microwave-Induced Iodine-Catalyzed Reactions under Solventless Conditions.
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- Molecules, 2010, v. 15, n. 4, p. 2520, doi. 10.3390/molecules15042520
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- Publication type:
- Article
20
Remarkable Iodine-Catalyzed Synthesis of Novel Pyrrole-Bearing N-Polyaromatic β-Lactams.
- Published in:
- Molecules, 2010, v. 15, n. 2, p. 1082, doi. 10.3390/molecules15021082
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- Publication type:
- Article
21
STEREOSELECTIVITY OF 3,3-DISUBSTITUTED β-LACTAM FORMATION VIA STAUDINGER REACTION.
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- Heterocyclic Communications, 2009, v. 15, n. 5, p. 365
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- Publication type:
- Article
22
AN EXPEDITIOUS SYNTHESIS OF 3-AMINO β-LACTAMS DERIVED FROM POLYAROMATIC COMPOUNDS.
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- Heterocyclic Communications, 2009, v. 15, n. 5, p. 323
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- Publication type:
- Article
23
HIGHLY STEREOSELECTIVE β-LACTAM SYNTHESIS VIA THE STAUDINGER REACTION USING POLY AROMATIC IMINES.
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- Heterocyclic Communications, 2009, v. 15, n. 3, p. 11
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- Publication type:
- Article
24
MICROWAVE-ASSISTED RUTHENIUM TRICHLORIDE-CATALYZED SYNTHESIS OF PYRROLE FUSED WITH INDOLE SYSTEM IN WATER.
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- Heterocyclic Communications, 2009, v. 15, n. 2, p. 121
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- Publication type:
- Article
25
NOVEL SYNTHESIS OF SUBSTITUTED PYRROLE BOUND TO INDOLINONE VIA MOLECULAR IODINE-CATALYZED REACTION.
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- Heterocyclic Communications, 2007, v. 13, n. 2/3, p. 109
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- Publication type:
- Article
26
BISMUTH NITRATE-MEDIATED DEPROTECTION OF OXIMES.
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- Synthetic Communications, 2002, v. 32, n. 13, p. 1917, doi. 10.1081/SCC-120004840
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- Article
27
Indium/Ammonium Chloride Mediated Selective Reduction of Aromatic Nitro Compounds: Practical Synthesis of 6-AminoChrysene.
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- Synthetic Communications, 2000, v. 30, n. 20, p. 3745, doi. 10.1080/00397910008087002
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- Article
28
Sodium Bismuthate Mediated Oxidation of Allylic and Benzylic Alcohols.
- Published in:
- Synthetic Communications, 2000, v. 30, n. 15, p. 2701, doi. 10.1080/00397910008086894
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- Publication type:
- Article