Asymmetric Synthesis of Halocyclized Products by Using Various Catalysts: A State‐of‐the‐Art Review DOI
Soumik De, Aritra Kumar Dan, Raghaba Sahu

et al.

European Journal of Organic Chemistry, Journal Year: 2022, Volume and Issue: 2022(32)

Published: July 25, 2022

Abstract Halogens play a crucial part in synthetic organic chemistry. Halo‐cyclized products hold numerous applications the pharmaceutical industries, agrochemicals, natural product synthesis, and material Thus, this review will discuss role of various catalysts, such as from metal‐catalysts to organocatalysts, under different conditions synthesize halocyclized products. The synthesis catalytic mechanisms underlying asymmetric transformations also be covered by emphasizing enantioselectivities, diastereoselectivities, regioselectivities existing pieces literature.

Language: Английский

Copper-catalyzed [3 + 2]-cycloaddition of α-halonitroalkenes with azomethine ylides: facile synthesis of multisubstituted pyrrolidines and pyrroles DOI
Vladimir Motornov, Andrey A. Tabolin, Yulia V. Nelyubina

et al.

Organic & Biomolecular Chemistry, Journal Year: 2021, Volume and Issue: 19(15), P. 3413 - 3427

Published: Jan. 1, 2021

An approach to multisubstituted pyrrolidines, pyrrolines and pyrroles is developed based on [3 + 2]-cycloaddition of α-halo (F, Cl, Br) nitroalkenes.

Language: Английский

Citations

23

The applications of catalytic asymmetric halocyclization in natural product synthesis DOI

Jiahang Yan,

Zhiqiang Zhou,

Qiaoqiao He

et al.

Organic Chemistry Frontiers, Journal Year: 2021, Volume and Issue: 9(2), P. 499 - 516

Published: Nov. 18, 2021

Catalytic asymmetric halocyclization of olefinic substrate has evolved rapidly and been well utilized as a practical strategy for constructing enantioenriched cyclic skeletons in natural product synthesis.

Language: Английский

Citations

23

Asymmetric Methods for Carbon‐Fluorine Bond Formation DOI

Attila Márió Remete,

Melinda Nonn,

Jorge Escorihuela

et al.

European Journal of Organic Chemistry, Journal Year: 2021, Volume and Issue: 2021(44), P. 5946 - 5974

Published: Oct. 6, 2021

Abstract As a consequence of the ever‐increasing relevance fluorinated drugs in medicinal chemistry, organofluorine chemistry has become hot topic research area during last decade. Asymmetric carbon‐fluorine bond‐forming reactions have enormously developed recent years with considerable findings related to novel and synthetic approaches. These new efforts contributed access growing number molecules complex natural or products high drug research. Illustrative examples methodologies, including organocatalytic processes, asymmetric syntheses phase‐transfer catalytic methods for enantioselective incorporation fluorine atom(s) into versatile molecular entities, are covered current Review, focusing on main contributions ten years.

Language: Английский

Citations

20

Recent Developments in Enantioselective Organocatalytic Cascade Reactions for the Construction of Halogenated Ring Systems DOI
Ana Maria Faísca Phillips, Armando J. L. Pombeiro

European Journal of Organic Chemistry, Journal Year: 2021, Volume and Issue: 2021(29), P. 3938 - 3969

Published: June 7, 2021

Abstract Chiral halogenated substances have many applications in pharmaceuticals, agrochemicals, and materials, such as polymers, liquid crystals intermediates synthesis. The presence of a halogen atom molecule can large effect its properties; for instance, halogens are used drugs to improve lipophilicity, membrane permeability absorption, even the blood‐brain barrier permeability. As highlighted this review, there nowadays range highly selective, versatile halogenating reagents, electrophilic, nucleophilic or radical nature, which operate under mild conditions, allowing late‐stage functionalization complex molecules cascade reactions. Recent developments organocatalyst design revealed novel Cinchona alkaloids derivatives, chiral phosphoric acids, amines, phosphines several bifunctional catalysts, mostly thiourea‐ squaramide‐based, introduced chirality, with high levels enantio‐ diastereoselection, formation one multiple centers single synthetic operation, shown. In review we survey literature published field from 2014 2020.

Language: Английский

Citations

19

Asymmetric Synthesis of Halocyclized Products by Using Various Catalysts: A State‐of‐the‐Art Review DOI
Soumik De, Aritra Kumar Dan, Raghaba Sahu

et al.

European Journal of Organic Chemistry, Journal Year: 2022, Volume and Issue: 2022(32)

Published: July 25, 2022

Abstract Halogens play a crucial part in synthetic organic chemistry. Halo‐cyclized products hold numerous applications the pharmaceutical industries, agrochemicals, natural product synthesis, and material Thus, this review will discuss role of various catalysts, such as from metal‐catalysts to organocatalysts, under different conditions synthesize halocyclized products. The synthesis catalytic mechanisms underlying asymmetric transformations also be covered by emphasizing enantioselectivities, diastereoselectivities, regioselectivities existing pieces literature.

Language: Английский

Citations

12