Cascade Phosphorylation/Cyclization of Propargylic Alcohols with R <sub>2</sub> P(O)–H: Access to Diverse 6-Phosphoryl-6-vinyl Indeno[2,1- <i>b</i> ]indoles

cyclization to afford the target products, which first demonstrates the cyclization as a new reaction mode compared with conventional cyclization pathways.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2026-04-22
DOI
https://doi.org/10.1021/acs.joc.5c03275
Primary Topic
Catalytic Alkyne Reactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Cascade Phosphorylation/Cyclization of Propargylic Alcohols with R 2 P(O)–H: Access to Diverse 6-Phosphoryl-6-vinyl Indeno[2,1- b ]indoles

Qiang Xiao, Mu‐Jia Luo, Ruchun Yang, An‐Xi Zhou et al.
The Journal of Organic Chemistry
Catalytic Alkyne Reactions
article

Cascade Phosphorylation/Cyclization of Propargylic Alcohols with R 2 P(O)–H: Access to Diverse 6-Phosphoryl-6-vinyl Indeno[2,1- b ]indoles

Qiang Xiao, Mu‐Jia Luo, Ruchun Yang, An‐Xi Zhou, Wan‐Fa Tian, X H Chen, Meng Liang, Xian‐Rong Song, Miaohao Dong
article en

Abstract

cyclization to afford the target products, which first demonstrates the cyclization as a new reaction mode compared with conventional cyclization pathways.

The Journal of Organic ChemistryVol. 91(17)
Shangrao Normal University (CN), Target (United States) (US), Jiangxi Science and Technology Normal University (CN)
National Natural Science Foundation of China, Natural Science Foundation of Jiangxi Province, Education Department of Jiangxi Province, Jiangxi Science and Technology Normal University
Openalex Percentile: Top 19%
Catalytic Alkyne Reactions
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