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Pt-Catalyzed Tandem 1,2-Acyloxy Migration/Intramolecular [3 + 2] Cycloaddition of Enynyl Esters

NIAID Data Ecosystem2026-03-06 收录

数据链接：

https://figshare.com/articles/dataset/Pt_Catalyzed_Tandem_1_2_Acyloxy_Migration_Intramolecular_3_2_Cycloaddition_of_Enynyl_Esters/2791531 数据链接链接失效反馈

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Pt-Catalyzed Tandem 1,2-Acyloxy Migration/Intramolecular [3 + 2] Cycloaddition of Enynyl Esters

应用场景：

创建时间：

2016-02-25

催化有机合成

C-C偶联反应

The cationic Ru–H complex was found to be an effective catalyst for the dehydrative C–H coupling of phenols with ketones to form the trisubstituted olefin products. The coupling of phenol with linear

NIAID Data Ecosystem100

An Electron-Rich Proazaphosphatrane for Isocyanate Trimerization to Isocyanurates

催化有机合成

异氰酸酯三聚反应

A facile synthesis of the new electron-rich, sterically hindered proazaphosphatrane shown above is described herein. This proazaphosphatrane catalyzes the cyclotrimerization of a wide variety of isocy

NIAID Data Ecosystem70

Stereoselective Epoxidation of Unfunctionalized Aliphatic Alkenes with a Macrocyclic Tetra-NHC Iron(II) Catalyst

立体选择性环氧化

催化有机合成

The development of atom-economical and earth-abundant catalysis for enantiopure epoxides is highly valuable since these strained chiral rings are key intermediates for many synthetic applications. How

Figshare2025-06-10 更新20

Iridium-Catalyzed Regio- and Diastereoselective Synthesis of C‑Substituted Piperazines

催化有机合成

药物分子构建

Piperazine rings are essential motifs frequently found in commercial drugs. However, synthetic methodologies are mainly limited to N-substituted piperazines, preventing structural diversity. Disclosed

NIAID Data Ecosystem80

The Crossed [2+2] Cycloaddition of 1-Phenylcyclopropene and 1-Bromo-2-phenylcyclopropene

环加成反应

有机合成方法

1-Bromo-2-phenylcyclopropene (2) underwent [2+2] dimerization to generate 1,2-dibromo-4,5-diphenyltricyclo[3.1.0.02,4]hexane (5), which was heated to form 1,2-dibromo-4,5-diphenylcyclohexa-1,4-diene (

NIAID Data Ecosystem40

Pt-Catalyzed Tandem 1,2-Acyloxy Migration/Intramolecular [3 + 2] Cycloaddition of Enynyl Esters

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