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Replication Data for: Accessing Chemo- and Regioselective Benzylic and Aromat...

B2FIND2026-05-30 收录

有机合成选择性

催化反应数据

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https://b2find.eudat.eu/dataset/2f031890-b192-58a0-882a-775d9e1f6d1f 数据链接链接失效反馈

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Data associated with the supplementary material (graphs, tables, figures, ...) of the article published in the journal 'ACS Catalysis', 2021, 11 (12). The data correspond to...

应用场景：

有机合成选择性

含氟化合物制备

The F···Ti bonding in the transition structures determines high trans- and syn-diastereoselectivities for aldol reactions of SF5-acetates with aldehydes in the presence of TiCl4 in the non-nucleophili

NIAID Data Ecosystem70

Amino Acid-Derived trans-N‑Chloroformylimidazolidinones: Scalable, Stereoselective Synthesis, Structure, and Utility

有机合成选择性

氨基酸衍生物

N-acyl imidazolidinones, which are key intermediates in the stereoselective synthesis of amino acids by “self-regeneration of stereochemistry” methods, are classically made by only moderately diastere

Figshare2019-05-15 更新40

Silicon-Tethered Strategy for Copper(I)-Catalyzed Stereo- and Regioselective Alkylboration of Alkynes

炔烃官能团化

有机合成选择性

Stereoselective silicon-tethered alkylboration of alkynes in the presence of a copper(I) catalyst and a diboron reagent provided the corresponding cyclic alkenylboronates in high yields (up to 99% yi

NIAID Data Ecosystem40

Selective Synthesis of N ‑Unsubstituted and N ‑Arylindoles by the Reaction of Arynes with Azirines

芳炔化学

有机合成选择性

The transition-metal-free and temperature-dependent highly selective reaction of arynes with 2H-azirines allowing the synthesis of either N-unsubstituted or N-arylindoles has been developed. At 60 °C,

NIAID Data Ecosystem60

Short Enantioselective Syntheses of trans -5-Alkylprolines from New Functionalized Amino Alcohols

非天然氨基酸

有机合成选择性

Amino alcohols, having an enol ether function, cyclized in acidic medium to give quantitatively diastereosomerically pure bicyclic compounds that were transformed in five steps in enantiopure trans-5-

NIAID Data Ecosystem40

Replication Data for: Accessing Chemo- and Regioselective Benzylic and Aromat...

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