An approach towards the construction of the tetracyclic skeleton of palhinine alkaloids-Reference-Cited by-同舟云学术

An approach towards the construction of the tetracyclic skeleton of palhinine alkaloids

Published:2020 Issue:16 Volume:7 Page:2243-2246
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Han Congcong¹²³⁴⁵,Chen Yang⁶⁷⁸³⁹,Ching Yin-Cheung¹⁰¹¹¹²¹³,Lee Chi-Sing¹⁰¹¹¹²¹³^ORCID,He Shuzhong¹²³⁴⁵^ORCID

Affiliation:

1. School of Pharmaceutical Sciences

2. and Guizhou Engineering Laboratory for Synthetic Drugs

3. Guizhou University

4. Guiyang

5. China

6. State Key Laboratory Breeding Base of Green Pesticide and Agricultural Bioengineering

7. Key Laboratory of Green Pesticide and Agricultural Bioengineering

8. Ministry of Education

9. Guiyang 550025

10. Department of Chemistry

11. Hong Kong Baptist University

12. Kowloon Tong

13. Hong Kong SAR

Abstract

A bifunctional Lewis acid catalyzed Diels–Alder/carbocyclization cascade process was developed for the rapid construction of the tetracyclic core of palhinine alkaloids.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Guizhou Province

Guizhou University

Hong Kong Baptist University

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2020/QO/D0QO00554A

Reference19 articles.

1. Palhinine A, a Novel Alkaloid from Palhinhaea cernua

2. Isopalhinine A, a Unique Pentacyclic Lycopodium Alkaloid from Palhinhaea cernua

3. Five new fawcettimine-related alkaloids from Lycopodium japonicum Thunb

4. Corrigendum to “Five new fawcettimine-related alkaloids from Lycopodium japoniucm Thunb.” [Fitoterapia (2013) 74 -81]

5. Total Synthesis of Lycopodium Alkaloids Palhinine A and Palhinine D

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