Literature DB >> 28993992

Sulfur-Containing Agrochemicals.

Ponnam Devendar1, Guang-Fu Yang2.   

Abstract

Modern agricultural chemistry has to support farmers by providing innovative agrochemicals. In this context, the introduction of sulfur atoms into an active ingredient is still an important tool in modulating the properties of new crop-protection compounds. More than 30% of today's agrochemicals contain at least one sulfur atom, mainly in fungicides, herbicides and insecticides. A number of recently developed sulfur-containing agrochemical candidates represent a novel class of chemical compounds with new modes of action, so we intend to highlight the emerging interest in commercially active sulfur-containing compounds. This chapter gives a comprehensive overview of selected leading sulfur-containing pesticidal chemical families namely: sulfonylureas, sulfonamides, sulfur-containing heterocyclics, thioureas, sulfides, sulfones, sulfoxides and sulfoximines. Also, the most suitable large-scale synthetic methods of the recently launched or provisionally approved sulfur-containing agrochemicals from respective chemical families have been highlighted.

Entities:  

Keywords:  Agrochemicals; Crop protection; Mode of action; Sulfur; Synthesis

Mesh:

Substances:

Year:  2017        PMID: 28993992     DOI: 10.1007/s41061-017-0169-9

Source DB:  PubMed          Journal:  Top Curr Chem (Cham)        ISSN: 2364-8961


  14 in total

1.  Photochemically Mediated Nickel-Catalyzed Synthesis of N-(Hetero)aryl Sulfamides.

Authors:  R Thomas Simons; Georgia E Scott; Anastasia Gant Kanegusuku; Jennifer L Roizen
Journal:  J Org Chem       Date:  2020-05-04       Impact factor: 4.354

2.  Stereospecific α-(hetero)arylation of sulfoximines and sulfonimidamides.

Authors:  Zachary P Shultz; Thomas Scattolin; Lukasz Wojtas; Justin M Lopchuk
Journal:  Nat Synth       Date:  2022-01-31

3.  One-Pot Synthesis of N-Iodo Sulfoximines from Sulfides.

Authors:  Anže Zupanc; Marjan Jereb
Journal:  J Org Chem       Date:  2021-03-25       Impact factor: 4.354

4.  Metal-Free Electrochemical Synthesis of Sulfonamides Directly from (Hetero)arenes, SO2 , and Amines.

Authors:  Stephan P Blum; Tarik Karakaya; Dieter Schollmeyer; Artis Klapars; Siegfried R Waldvogel
Journal:  Angew Chem Int Ed Engl       Date:  2021-02-02       Impact factor: 15.336

5.  Sulfonamide Synthesis via Calcium Triflimide Activation of Sulfonyl Fluorides.

Authors:  Paramita Mukherjee; Cristian P Woroch; Leah Cleary; Mark Rusznak; Ryan W Franzese; Matthew R Reese; Joseph W Tucker; John M Humphrey; Sarah M Etuk; Sabrina C Kwan; Christopher W Am Ende; Nicholas D Ball
Journal:  Org Lett       Date:  2018-06-11       Impact factor: 6.072

6.  Chemical synthesis, crystal structure, versatile evaluation of their biological activities and molecular simulations of novel pyrithiobac derivatives.

Authors:  Ren-Jun Wu; Kai-Xuan Zhou; Haijin Yang; Guo-Qing Song; Yong-Hong Li; Jia-Xin Fu; Xiao Zhang; Shu-Jing Yu; Li-Zhong Wang; Li-Xia Xiong; Cong-Wei Niu; Fu-Hang Song; Haitao Yang; Jian-Guo Wang
Journal:  Eur J Med Chem       Date:  2019-02-14       Impact factor: 6.514

7.  Decatungstate-Catalyzed C(sp3)-H Sulfinylation: Rapid Access to Diverse Organosulfur Functionality.

Authors:  Patrick J Sarver; Noah B Bissonnette; David W C MacMillan
Journal:  J Am Chem Soc       Date:  2021-06-23       Impact factor: 15.419

8.  Modular Synthesis of Alkenyl Sulfamates and β-Ketosulfonamides via Sulfur(VI) Fluoride Exchange (SuFEx) Click Chemistry and Photomediated 1,3-Rearrangement.

Authors:  Felipe Cesar Sousa E Silva; Katarzyna Doktor; Quentin Michaudel
Journal:  Org Lett       Date:  2021-06-20       Impact factor: 6.072

9.  Silyloxymethanesulfinate as a sulfoxylate equivalent for the modular synthesis of sulfones and sulfonyl derivatives.

Authors:  Dae-Kwon Kim; Hyun-Suk Um; Hoyoon Park; Seonwoo Kim; Jin Choi; Chulbom Lee
Journal:  Chem Sci       Date:  2020-10-22       Impact factor: 9.825

10.  Hydroxylamine-Derived Reagent as a Dual Oxidant and Amino Group Donor for the Iron-Catalyzed Preparation of Unprotected Sulfinamides from Thiols.

Authors:  Sayanti Chatterjee; Szabolcs Makai; Bill Morandi
Journal:  Angew Chem Int Ed Engl       Date:  2020-11-10       Impact factor: 16.823

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