Base‐Promoted One‐Pot Synthesis of Phthalans from 1,3‐Enynyl Alcohols and Allylic(propargylic) Bromides

Abstract A synthetic method that relies on base‐promoted allylation(propargylation)/propargyl‐allenyl isomerization/dehydro‐Diels−Alder cascade of 1,3‐enynyl alcohols for the synthesis of structurally diverse phthalan derivatives under metal‐free mild reaction conditions is described. Moreover, the protocol could be further expanded to the synthesis of 3,5‐disubstituted‐5,7‐dihydrofuro[3,4‐ b ]pyridines simply by changing the allyl or propargyl bromides to 2‐bromoacetonitrile.

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Publication Details

Journal
Asian Journal of Organic Chemistry
Published
2025-10-04
DOI
https://doi.org/10.1002/ajoc.202500615
Citations
1
Primary Topic
Catalytic Alkyne Reactions
Type
article
Field-Weighted Citation Impact
0.94
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article

Base‐Promoted One‐Pot Synthesis of Phthalans from 1,3‐Enynyl Alcohols and Allylic(propargylic) Bromides

Weidong Rao, Qing Liu, Yili Shen
1 citations
Asian Journal of Organic Chemistry
Catalytic Alkyne Reactions
0.94
article

Base‐Promoted One‐Pot Synthesis of Phthalans from 1,3‐Enynyl Alcohols and Allylic(propargylic) Bromides

Weidong Rao, Qing Liu, Yili Shen
article en
1 citations

Abstract

Abstract A synthetic method that relies on base‐promoted allylation(propargylation)/propargyl‐allenyl isomerization/dehydro‐Diels−Alder cascade of 1,3‐enynyl alcohols for the synthesis of structurally diverse phthalan derivatives under metal‐free mild reaction conditions is described. Moreover, the protocol could be further expanded to the synthesis of 3,5‐disubstituted‐5,7‐dihydrofuro[3,4‐ b ]pyridines simply by changing the allyl or propargyl bromides to 2‐bromoacetonitrile.

Asian Journal of Organic ChemistryVol. 14(12)
Nanjing Forestry University (CN)
Openalex Percentile: Top 21%
Catalytic Alkyne Reactions
0.94
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