Recent advances in organocatalytic asymmetric oxa-Michael addition triggered cascade reactions

文献情報

出版日 2020-08-14

DOI 10.1039/D0QO00631A

インパクトファクター 5.281

著者

Yu Wang, Da-Ming Du

原文を見る

要旨

The oxa-Michael cascade reaction, as an important part of the Michael reaction, has also been significantly developed over the recent decade. This is because the problem of the reactivity and selectivity of the addition reactions of oxygen nucleophiles to conjugated systems has been solved by different organocatalysts and reaction conditions. Therefore, using various efficient strategies, many novel and potentially bioactive chiral compounds with excellent yields and stereoselectivities have been synthesized. In this review, we summarize the recent advances in organocatalytic asymmetric oxa-Michael addition triggered cascade reactions for the stereoselective synthesis of heterocyclic compounds.

掲載誌

Organic Chemistry Frontiers

CiteScore: 7.8

自己引用率: 8.7%

年間論文数: 724

Organic Chemistry Frontiers publishes high-quality research from across organic chemistry. Emphases are placed on studies that make significant contributions to the field of organic chemistry by reporting either new or significantly improved protocols or methodologies. Topics include, but are not limited to the following: Organic synthesis Development of synthetic methodologies Catalysis Natural products Functional organic materials Supramolecular and macromolecular chemistry Physical and computational organic chemistry

Recent advances in organocatalytic asymmetric oxa-Michael addition triggered cascade reactions

文献情報

おすすめジャーナル

関連文献

N-ethyl-N-methylpyrrolidinium bis(fluorosulfonyl)imide-electrospun polyvinylidene fluoride composite electrolytes: characterization and lithium cell studies

Sensitized ZnO nanorod assemblies to detect heavy metal contaminated phytomedicines: spectroscopic and simulation studies

Polar solvent fluctuations drive proton transfer in hydrogen bonded complexes of carboxylic acid with pyridines: NMR, IR and ab initio MD study

Molecular hydrogen production from amorphous solid water during low energy electron irradiation

Intermolecular structure and hydrogen-bonding in liquid 1,2-propylene carbonate and 1,2-glycerol carbonate determined by neutron scattering

The impact of the structuring of hydrotropes in water on the mesoscale solubilisation of a third hydrophobic component

Back cover

Molecular qubits based on potentially nuclear-spin-free nickel ions

The discrete nature of inhomogeneity: the initial stages and local configurations of TiOPc during bilayer growth on Ag(111)

Theoretical investigation of gas-phase molecular complex formation between 2-hydroxy thiophenol and a water molecule

こちらもおすすめ

4'-ブロモビフェニル-3-メトークシーディ.ActionBarはどのように保存すればよいですか？

間甲苯乙腈とは何ですか？

2-異丙基フェニルヒドラジン塩酸塩とは何ですか？

5-(4-クロロフェニル)-4H-1,2,4-三氮唑-3-アミンを取り扱う際の実験室安全事項は何ですか？

去甲基雷贝拉唑硫醚はどのように合成されますか？

2-ブロモ-5-フロロ-N-(2-フェノールメチル)ベンゼンウレアは安全ですか？

対甲苯磺酸酯-四聚乙二醇-四氢吡喃醚の物理化学的性質は何ですか？

2-(3-(二氟甲基)-4-氟苯基)-4,4,5,5-四甲基-1,3,2-二噁硼戊環はどのように保存すればよいですか？

6-アミノ-5-クロロ-2-シクロプロピルピリミジンカルボン酸の代替品はありますか？

5-クロロベンゾ[1,3]二オキセイン-4-アミンに適用される法規ガイドラインは何ですか？

掲載誌

Organic Chemistry Frontiers

おすすめ化合物

4,5-Dimethyl-1,3-dioxolan-2-one

Ethyl 4-amino-3-phenyl-1H-pyrazole-5-carboxylate

Iodide

2-Hydroxy-5-iodo-4-methylbenzoic acid

(1S)-1,5-Anhydro-2-O-alpha-L-arabinopyranosyl-1-[5-hydroxy-7-({6-O-[3-(4-hydroxy-3-methoxyphenyl)propanoyl]-beta-D-glucopyranosyl}oxy)-2-(4-hydroxyphenyl)-4-oxo-4H-chromen-6-yl]-D-glucitol

おすすめサプライヤー