Literature DB >> 26760899

Chemistry of Ketene N,S-Acetals: An Overview.

Lin Zhang1, Jinhuan Dong1, Xianxiu Xu1, Qun Liu1.   

Abstract

Push-pull alkenes, which bear electron-donating and -accepting group(s) at both termini of a C═C double bond, respectively, are of interest not only for their unique electronic properties but also for their importance as versatile building blocks in organic synthesis. In the world of ketene acetals having the push-pull alkene skeleton, ketene N,S-acetal is most likely the biggest family according to the number and types of these compounds. The first ketene N,S-acetal compound was reported in 1956. As a cyclic ketene N,S-acetal compound, nithiazine, the first lead structure of neonicotinoid insecticides, was reported in 1978. The characteristics of ketene N,S-acetals, which have the structural feature of ketene S,S-acetals and enaminones, make them versatile and easy to use, especially in cyclization and multicomponent reactions for the synthesis of various heterocyclic systems and related natural products. There has been an increasing wealth of information about the synthesis and synthetic applications of ketene N,S-acetals, especially, in recent years. This review provides comprehensive knowledge on the chemistry of ketene N,S-acetals.

Entities:  

Year:  2016        PMID: 26760899     DOI: 10.1021/acs.chemrev.5b00360

Source DB:  PubMed          Journal:  Chem Rev        ISSN: 0009-2665            Impact factor:   60.622


  10 in total

1.  Synthesis of diverse N-acyl-pyrazoles via cyclocondensation of hydrazides with α-oxeketene dithioacetal.

Authors:  Bruna Á Pereira; Alcione V de Bastos; Wystan K O Teixeira; Sidnei Moura E Silva; Alex F C Flores; Darlene C Flores
Journal:  Mol Divers       Date:  2017-08-08       Impact factor: 2.943

2.  A fluorescent target-guided Paal-Knorr reaction.

Authors:  Sachin B Wagh; Vladimir Maslivetc; James J La Clair; Alexander Kornienko
Journal:  RSC Adv       Date:  2020-10-07       Impact factor: 4.036

3.  4-Trifluoromethyl-p-quinols as dielectrophiles: three-component, double nucleophilic addition/aromatization reactions.

Authors:  Jinhuan Dong; Lou Shi; Ling Pan; Xianxiu Xu; Qun Liu
Journal:  Sci Rep       Date:  2016-06-01       Impact factor: 4.379

4.  One-pot sequential synthesis of tetrasubstituted thiophenes via sulfur ylide-like intermediates.

Authors:  Jun Ki Kim; Hwan Jung Lim; Kyung Chae Jeong; Seong Jun Park
Journal:  Beilstein J Org Chem       Date:  2018-01-26       Impact factor: 2.883

Review 5.  Transition-metal-catalyzed remote C-H functionalization of thioethers.

Authors:  Xiao-Qing Feng; He-Cheng Wang; Zhi Li; Long Tang; Xiaoqiang Sun; Ke Yang
Journal:  RSC Adv       Date:  2022-04-07       Impact factor: 3.361

6.  Simple synthesis of new imidazopyridinone, pyridopyrimidinone, and thiazolopyridinone derivatives and optimization of reaction parameters using response surface methodology.

Authors:  Fahimeh Sadat Hosseini; Mohammad Bayat
Journal:  RSC Adv       Date:  2019-09-25       Impact factor: 4.036

7.  Catalyst-free four-component domino synthetic approach toward versatile multicyclic spirooxindole pyran scaffolds.

Authors:  Aref Mohammadi; Mohammad Bayat; Shima Nasri
Journal:  RSC Adv       Date:  2019-05-28       Impact factor: 3.361

Review 8.  Nitroketene N,S-acetals: synergistic building blocks for the synthesis of heterocycles.

Authors:  Sarfaraz Khan; Habibur Rahman; Md Musawwer Khan
Journal:  RSC Adv       Date:  2019-05-09       Impact factor: 4.036

9.  An efficient synthesis of new imidazo[1,2-a]pyridine-6-carbohydrazide and pyrido[1,2-a]pyrimidine-7-carbohydrazide derivatives via a five-component cascade reaction.

Authors:  Hajar Hosseini; Mohammad Bayat
Journal:  RSC Adv       Date:  2019-03-05       Impact factor: 4.036

10.  Synthesis of 5-amino-N'-(9H-fluoren-9-ylidene)-8-nitro-7-aryl-1,2,3,7-tetrahydroimidazo[1,2-a]pyridine-6-carbohydrazide derivatives based on heterocyclic ketene aminals.

Authors:  Hajar Hosseini; Mohammad Bayat
Journal:  RSC Adv       Date:  2018-12-11       Impact factor: 4.036

  10 in total

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