Pd-Catalyzed Tandem [5 + 2] Cycloaddition/Ring Contraction of Phthalide-Derived Alkenes and Vinylethylene Carbonates for the Construction of Benzo-[5,5]-spiroketal Lactones-Reference-Cited by-同舟云学术

Pd-Catalyzed Tandem [5 + 2] Cycloaddition/Ring Contraction of Phthalide-Derived Alkenes and Vinylethylene Carbonates for the Construction of Benzo-[5,5]-spiroketal Lactones

Published:2022-05-02 Issue:18 Volume:24 Page:3363-3367
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Xiong Qiang¹,Lu Ji²,Shi Liu¹,Ran Guang-Yao¹^ORCID

Affiliation:

1. Department of Medicinal Chemistry, College of Pharmacy, Chongqing Medical University, Chongqing 400016, China

2. College of Pharmacy, Southwest Medical University, Luzhou 646000, China

Funder

Natural Science Foundation of Chongqing

Chongqing Medical University

National Natural Science Foundation of China

Sichuan Province

MOE Key Laboratory of Drug Targeting and Drug Delivery System, West China School of Pharmacy, Sichuan University

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.2c01114

Reference51 articles.

1. Isolation, biological activity and synthesis of benzannulated spiroketal natural products

2. Spirolactones: Recent Advances in Natural Products, Bioactive Compounds and Synthetic Strategies

3. Recent progress in the isolation, bioactivity, biosynthesis, and total synthesis of natural spiroketals

4. Recent advances in the synthesis of oxaspirolactones and their application in the total synthesis of related natural products

5. Strategies for the construction of γ-spirocyclic butenolides in natural product synthesis

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