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Raw Experimental Data for "π-Radical Cascade to a Chiral Saddle-Shaped Peropyrene"

Name: Raw Experimental Data for "π-Radical Cascade to a Chiral Saddle-Shaped Peropyrene"
Creator: University of Zurich; University of Freiburg; University of Granada
Published: 2023-11-28T00:00:00+08:00

Zenodo2023-11-28 更新2026-04-07 收录

π-自由基级联反应

手性化合物合成

数据链接：

https://zenodo.org/doi/10.5281/zenodo.10212222 数据链接链接失效反馈

官方服务：

资源简介：

Raw experimental data associated with the manuscript: "π-Radical Cascade to a Chiral Saddle-Shaped Peropyrene"

应用场景：

提供机构：

University of Zurich; University of Freiburg; University of Granada

创建时间：

2023-11-28

有机合成光催化

手性化合物合成

Cocatalysis by pivalic acid or copper bromide allows a very fast, clean, and high-yielding palladium-catalyzed coupling of a large array of aryl, thienyl, and pyridyl halides with cyclic nitrones, inc

NIAID Data Ecosystem50

Highly Enantioselective Synthesis of Chiral Allenes by Sequential Creation of Stereogenic Center and Chirality Transfer in a Single Pot Operation

手性化合物合成

立体选择性合成

Chiral allenes are readily accessed in a single pot operation in the reaction of terminal alkynes, aldehydes, chiral secondary amines, and zinc halides in good yields (up to 77% yield) and excellent e

NIAID Data Ecosystem40

The Prins Reaction Using Ketones: Rationalization and Application toward the Synthesis of the Portentol Skeleton

有机合成方法

手性化合物合成

We report a TMSI-promoted Prins cyclization reaction with ketones as carbonyl partners to prepare polysubstituted chiral spirotetrahydropyrans. In the presence of racemic 2-methylcyclohexanone a dynam

Figshare2016-02-22 更新10

A Powerful New Construction of Complex Chiral Polycycles by an Indium(III)-Catalyzed Cationic Cascade

手性化合物合成

三价金属催化反应

InI3 and InBr3 have been found to be effective catalysts for the π activation of CC bonds to initiate the conversion of chiral propargylic alcohols or silyl ethers to polycyclic products in excellent

Figshare2016-02-23 更新40

Highly Enantioselective Construction of Trifluoromethylated All-Carbon Quaternary Stereocenters via Nickel-Catalyzed Friedel–Crafts Alkylation Reaction

催化不对称合成

手性化合物合成

A highly enantioselective Friedel–Crafts alkylation reaction of indoles with β-CF3-β-disubstituted nitroalkenes was achieved using a Ni(ClO4)2–bisoxazoline complex as a catalyst, which afforded indol

NIAID Data Ecosystem30

Raw Experimental Data for "π-Radical Cascade to a Chiral Saddle-Shaped Peropyrene"

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