Highly Stereoselective Asymmetric Total Synthesis of (−)-Jimenezin via Sequential Intramolecular Amide Enolate Alkylation-Reference-Cited by-同舟云学术

Highly Stereoselective Asymmetric Total Synthesis of (−)-Jimenezin via Sequential Intramolecular Amide Enolate Alkylation

Published:2022-02-23 Issue:8 Volume:24 Page:1652-1656
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Lu Thien Nhan¹,Kwak Minjung¹,Samala Mallesham¹,Son Minji¹,Hwang Jungjoong¹,Mandava Suresh¹,Pham Thuy Trang¹,Park Haeil¹,Kim Hyoungsu²^ORCID,Kim Deukjoon³^ORCID,Lee Jongkook¹^ORCID

Affiliation:

1. College of Pharmacy, Kangwon National University, 1 Kangwondaehak-gil, Chuncheon, Gangwon-do 24341, Republic of Korea

2. College of Pharmacy, Ajou University, Suwon, Gyeonggi-do 16499, Republic of Korea

3. College of Pharmacy, Seoul National University, Seoul 08826, Republic of Korea

Funder

National Research Foundation of Korea

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.2c00196

Reference23 articles.

1. Jimenezin, a Novel Annonaceous Acetogenin from the Seeds of Rollinia mucosa Containing Adjacent Tetrahydrofuran−Tetrahydropyran Ring Systems,1

2. Die relative Konfiguration der ausAnnona squamosaisolierten Acetogenine Annonin I (Squamocin) und Annonin VI1

3. Total Synthesis of a New Cytotoxic Acetogenin, Jimenezin, and the Revised Structure

4. Stereoselective synthesis of (−)-jimenezin

5. Total Synthesis of Jimenezin via an Intramolecular Allylboration

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