Literature DB >> 35423435

Synthesis and applications of sodium sulfinates (RSO2Na): a powerful building block for the synthesis of organosulfur compounds.

Raju Jannapu Reddy1, Arram Haritha Kumari1.   

Abstract

This review highlights the preparation of sodium sulfinates (RSO2Na) 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. Remarkable advancement has been made in synthesizing thiosulfonates, sulfonamides, sulfides, and sulfones, including vinyl sulfones, allyl sulfones, and β-keto sulfones. The significant achievement of developing sulfonyl radical-triggered ring-closing sulfonylation and multicomponent reactions is also thoroughly discussed. Of note, the most promising site-selective C-H sulfonylation, photoredox catalytic transformations and electrochemical synthesis of sodium sulfinates are also demonstrated. Holistically, this review provides a unique and comprehensive overview of sodium sulfinates, which summarizes 355 core references up to March 2020. The chemistry of sodium sulfinate salts is divided into several sections based on the classes of sulfur-containing compounds with some critical mechanistic insights that are also disclosed. This journal is © The Royal Society of Chemistry.

Entities:  

Year:  2021        PMID: 35423435      PMCID: PMC8695481          DOI: 10.1039/d0ra09759d

Source DB:  PubMed          Journal:  RSC Adv        ISSN: 2046-2069            Impact factor:   3.361


  157 in total

1.  Transition-Metal-Free Regioselective One-Pot Synthesis of Aryl Sulfones from Sodium Sulfinates via Quinone Imine Ketal.

Authors:  Priyanka Halder; Vivek T Humne; Santosh B Mhaske
Journal:  J Org Chem       Date:  2019-01-23       Impact factor: 4.354

2.  Silver or cerium-promoted free radical cascade difunctionalization of o-vinylanilides with sodium aryl- or alkylsulfinates.

Authors:  Jilai Wu; Yuanyuan Zong; Chunxia Zhao; Qinqin Yan; Lixian Sun; Yiming Li; Jincan Zhao; Yaxin Ge; Zejiang Li
Journal:  Org Biomol Chem       Date:  2019-01-23       Impact factor: 3.876

3.  Copper-Catalyzed Oxysulfenylation of Enolates with Sodium Sulfinates: A Strategy To Construct Sulfenylated Cyclic Ethers.

Authors:  Yinglan Gao; Yang Gao; Xiaodong Tang; Jianwen Peng; Miao Hu; Wanqing Wu; Huanfeng Jiang
Journal:  Org Lett       Date:  2016-02-25       Impact factor: 6.005

4.  Transition-Metal-Free Selective Oxidative C(sp3)-S/Se Coupling of Oxindoles, Tetralone, and Arylacetamides: Synthesis of Unsymmetrical Organochalcogenides.

Authors:  Ch Durga Prasad; Moh Sattar; Sangit Kumar
Journal:  Org Lett       Date:  2017-02-09       Impact factor: 6.005

5.  Multiple-functionalizations of terminal alkynes with sodium sulfinates and tert-butyl nitrite: facile synthesis of 2H-azirines.

Authors:  Xingyi He; Xin Yue; Lei Zhang; Shuang Wu; Ming Hu; Jin-Heng Li
Journal:  Chem Commun (Camb)       Date:  2019-03-19       Impact factor: 6.222

6.  Odorless, One-Pot Regio- and Stereoselective Iodothiolation of Alkynes with Sodium Arenesulfinates under Metal-Free Conditions in Water.

Authors:  Ya-mei Lin; Guo-ping Lu; Chun Cai; Wen-bin Yi
Journal:  Org Lett       Date:  2015-06-17       Impact factor: 6.005

7.  Vitamin a synthesis by sulfone alkyaltion-elimination. C15 halide, C5 hydroxy sulfone approach.

Authors:  G L Olson; H C Cheung; K D Morgan; C Neukom; G Saucy
Journal:  J Org Chem       Date:  1976-10-01       Impact factor: 4.354

8.  Iridium-catalyzed, regio- and enantioselective allylic substitution with aromatic and aliphatic sulfinates.

Authors:  Mitsuhiro Ueda; John F Hartwig
Journal:  Org Lett       Date:  2010-01-01       Impact factor: 6.005

9.  Direct synthesis of fluorinated heteroarylether bioisosteres.

Authors:  Qianghui Zhou; Alessandro Ruffoni; Ryan Gianatassio; Yuta Fujiwara; Eran Sella; Doron Shabat; Phil S Baran
Journal:  Angew Chem Int Ed Engl       Date:  2013-03-04       Impact factor: 15.336

10.  Synthesis of Sulfonylated Lactams by Copper-Mediated Aminosulfonylation of 2-Vinylbenzamides with Sodium Sulfinates.

Authors:  Li-Jing Wang; Jia-Min Chen; Wei Dong; Cong-Ying Hou; Mingming Pang; Wen-Bo Jin; Fu-Gui Dong; Zhi-Dong Xu; Wei Li
Journal:  J Org Chem       Date:  2019-02-01       Impact factor: 4.354

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  3 in total

1.  Selective removal of toxic organic dyes using Trӧger base-containing sulfone copolymers made from a metal-free thiol-yne click reaction followed by oxidation.

Authors:  Noorullah Baig; Suchetha Shetty; Moustafa Sherief Moustafa; Saleh Al-Mousawi; Bassam Alameddine
Journal:  RSC Adv       Date:  2021-06-15       Impact factor: 4.036

2.  Reductant-Free Cross-Electrophile Synthesis of Di(hetero)arylmethanes by Palladium-Catalyzed Desulfinative C-C Coupling.

Authors:  Janette McKnight; Andre Shavnya; Neal W Sach; David C Blakemore; Ian B Moses; Michael C Willis
Journal:  Angew Chem Int Ed Engl       Date:  2022-03-14       Impact factor: 16.823

3.  Scalable, Chemoselective Nickel Electrocatalytic Sulfinylation of Aryl Halides with SO2.

Authors:  Terry Shing-Bong Lou; Yu Kawamata; Tamara Ewing; Guillermo A Correa-Otero; Michael R Collins; Phil S Baran
Journal:  Angew Chem Int Ed Engl       Date:  2022-08-03       Impact factor: 16.823

  3 in total

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