Total Synthesis of Eucalyptusdimers A–C

]chromene framework with excellent regioselectivity and stereoselectivity, incorporating four chiral centers and one prochiral center in a single step. In addition, a Vilsmeier-Haack formylation followed by Friedel-Crafts alkylation was employed to complete the target molecules.

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Publication Details

Journal
Organic Letters
Published
2026-04-22
DOI
https://doi.org/10.1021/acs.orglett.6c01175
Primary Topic
Natural Compound Pharmacology Studies
Type
article
Field-Weighted Citation Impact
0.00

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article

Total Synthesis of Eucalyptusdimers A–C

M M Wang, Shengfu Duan, Zhixiang Xie, Minghan Li et al.
Organic Letters
Natural Compound Pharmacology Studies
article

Total Synthesis of Eucalyptusdimers A–C

M M Wang, Shengfu Duan, Zhixiang Xie, Minghan Li, Mengyao Sun
article en

Abstract

]chromene framework with excellent regioselectivity and stereoselectivity, incorporating four chiral centers and one prochiral center in a single step. In addition, a Vilsmeier-Haack formylation followed by Friedel-Crafts alkylation was employed to complete the target molecules.

Organic LettersVol. 28(17)
State Key Laboratory of Chemical Engineering (CN), Lanzhou University (CN)
National Natural Science Foundation of China
Zero hunger
Openalex Percentile: Top 18%
Natural Compound Pharmacology Studies
DOISourceOpenAlex
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