CH活化合成Phochrodines A-C

IF 3.6 2区化学 Q1 CHEMISTRY, ORGANIC Journal of Organic Chemistry Pub Date : 2025-04-09 DOI:10.1021/acs.joc.5c00210

Sopan Pralhad Khandare, Chloe Xin Ying Peh, Roderick W. Bates

引用次数: 0

摘要

采用ch活化法和钯催化羰基化法制备了phochrodine A、B和C。为了避免区域选择性问题，利用了共同中间体的固有对称性。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

摘要图片

查看原文

微信好友朋友圈 QQ好友复制链接

本刊更多论文

Synthesis of Phochrodines A–C by CH Activation

Phochrodines A, B, and C have been synthesized using a CH-activation protocol and palladium-catalyzed carbonylation. To avoid issues of regioselectivity, the inherent symmetry of a common intermediate was exploited.

求助全文

通过发布文献求助，成功后即可免费获取论文全文。去求助

来源期刊

Journal of Organic Chemistry 化学-有机化学

CiteScore

6.20

自引率

11.10%

发文量

1467

审稿时长

2 months

期刊介绍： Journal of Organic Chemistry welcomes original contributions of fundamental research in all branches of the theory and practice of organic chemistry. In selecting manuscripts for publication, the editors place emphasis on the quality and novelty of the work, as well as the breadth of interest to the organic chemistry community.

期刊最新文献

Electrochemical Synthesis of α,α-Dichlorosulfoxides from Methyl Sulfoxides with Dichloromethane. Mechanistic Dichotomy in Sulfate Radical Anion-Mediated Oxidative Synthesis of Activated N-Hydroxysuccinimide Esters. Generating Molecular Diversity via Addition of Nucleophiles to Electron-Deficient [3]Dendralenes: An Exploratory Study. Mechanistic Insights into the Regioselective (3 + 2) Cycloaddition of Unsymmetrical Cyclopropenones with Elemental Sulfur: Experimental and Computational Studies. Synthesis of 2-Thioxo-1,3-benzothiazin-4-one by PPh3-Promoted Desulfurative [4 + 2] Annulation.