4 results match your criteria: "Osmania University Hyderabad 500 007 India rajuchem77@osmania.ac.in rajuchem08@yahoo.co.in.[Affiliation]"
RSC Adv
March 2021
Department of Chemistry, University College of Science, Osmania University Hyderabad 500 007 India
This review highlights the preparation of sodium sulfinates (RSONa) and their multifaceted synthetic applications. Substantial progress has been made over the last decade in the utilization of sodium sulfinates emerging as sulfonylating, sulfenylating or sulfinylating reagents, depending on reaction conditions. Sodium sulfinates act as versatile building blocks for preparing many valuable organosulfur compounds through S-S, N-S, and C-S bond-forming reactions.
View Article and Find Full Text PDFOrg Biomol Chem
April 2021
Department of Chemistry, University College of Science, Osmania University, Hyderabad 500 007, India.
This review mainly focuses on recent developments in the preparation of β-keto sulfones and their extensive synthetic applications. New prospects for the synthesis of β-keto thiosulfones have also been highlighted. Over the last decade, there has been exponential growth in the direct construction of β-keto sulfones using a wide variety of keto and sulfonyl precursors.
View Article and Find Full Text PDFOrg Biomol Chem
May 2020
X-ray Crystallography, CSIR-National Chemical Laboratory, Pune 411 008, India.
A unique phenylboronic acid-catalyzed dimerization-sulfonylation of S-benzyl thiosulfonates has been disclosed. A metal-free tandem construction of S-S and C-S bonds is an operationally simple method to access a wide range of benzyl disulfanylsulfone derivatives in high to excellent yields. Moreover, the robustness of this tandem transformation has been demonstrated by gram-scale reactions, and a plausible mechanism is also proposed.
View Article and Find Full Text PDFRSC Adv
November 2018
Department of Chemistry, Osmania University Hyderabad 500 007 India
A practical, highly flexible and eco-friendly method has been developed for the synthesis of allyl thiosulfonates using Morita-Baylis-Hillman (MBH) allyl bromides and sodium arylthiosulfonates, which were readily assembled without any reagent/catalyst. Moreover, the allyl thiosulfonates were successfully transformed into a set of two synthetically viable diallyl disulfanes and unsymmetrical allyl disulfanes in the presence of CsCO. The present protocols are operationally simple and convenient to generate a wide range of functionalized allyl thiosulfonates and allyl disulfanes in good to excellent yields.
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