Search Results - "Ghosal, Nirnita"
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Zwitterionic imidazolium salt: An efficient organocatalyst for tetrahydropyranylation of alcohols
Published in Synthetic communications (18-10-2017)“…An aprotic imidazole based zwitterionic-salt, 4-(3-methylimidazolium)-butane sulfonate has been found to be an efficient organocatalyst for…”
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An Efficient Synthesis of Oxazolidines by Tandem Ring‐Opening / Closing Reaction of Ts‐Aziridine Using Formic Acid
Published in ChemistrySelect (Weinheim) (09-10-2018)“…Synthesis of oxazolidines has been reported from aziridines by the reaction with formic acid and formaldehyde in neat conditions. We have also observed a…”
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A Mild and Efficient Method for the Syntheses and Regioselective Ring-Opening of Aziridines
Published in SynOpen (2017) (01-03-2017)“…We have developed a new synthetic method for the synthesis of aziridines using Chloramine-T as an effective reagent in the presence of NH2OH·HCl and NaIO4. We…”
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Combination of NH2OH·HCl and NaIO4: a new and mild reagent for the synthesis of vicinal diiodo carbonyl compounds
Published in ARKIVOC free online journal of organic chemistry (13-12-2016)Get full text
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Conjugated Addition of Amines to Electron Deficient Alkenes: A Green Approach
Published in Chimica Techno Acta (14-07-2017)“…A very simple approach has been developed for conjugate addition of a variety of aliphatic and aromatic amines to electron deficient alkenes in presence tea…”
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Conversion of aziridines to oxazolidines through geminal difunctionalization of vinyl arenes or by tandem ring-opening/closing reaction of aziridine itself
Published in Tetrahedron letters (03-08-2016)“…[Display omitted] •Synthesis of 1,3-oxazolidines was developed by two different approaches.•Aziridines were used in the first approach instead of amino…”
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CuO Nanoparticles as a Simple and Efficient Green Catalyst for the Aziridine Ring‐Opening: Examination of a Broad Range of Nucleophiles
Published in ChemistrySelect (Weinheim) (23-04-2020)“…It has been observed that CuO nanoparticles act as effective and reusable catalyst for the ring‐opening reaction of aziridines with a wide range of…”
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Scope and Limitations of Leuckart‐Wallach‐Type Reductive Amination: Chemoselective Synthesis of Tertiary Amines from Aldehydes under Neat Conditions
Published in ChemistrySelect (Weinheim) (23-04-2018)“…We have developed a convenient method to synthesize tertiary amines selectively with a variety of aldehydes and primary amines using commercially available…”
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