Recent Advances in the Synthesis of Stemona Alkaloids-Reference-Cited by-同舟云学术

Recent Advances in the Synthesis of Stemona Alkaloids

Published:2015-06 Issue:6 Volume:10 Page:1934578X1501000
ISSN:1934-578X
Container-title:Natural Product Communications
language:en
Short-container-title:Natural Product Communications

Author:

Liu Xiao-Yu¹,Wang Feng-Peng¹

Affiliation:

1. Key Laboratory of Drug Targeting and Drug Delivery Systems of the Ministry of Education, Department of Chemistry of Medicinal Natural Products, West China College of Pharmacy, Sichuan University No. 17, Duan 3, Remin Nan Road, Chengdu 610041, P.R. China

Abstract

Stemona alkaloids, featuring polycyclic structures and interesting bioactivities, constitute a distinct class from the Stemonaceae family. In this review, recent advances in the synthesis of these unique alkaloids are briefly discussed, highlighting the application of novel synthetic strategies to access the core structures, as well as creative solutions to the installation of multiple stereogenic centers. The literature reviewed in this article covers the publications from 2010 to November 2014, a period that witnessed the prosperity of the synthesis of Stemona alkaloids.

Publisher

SAGE Publications

Subject

Complementary and alternative medicine,Plant Science,Drug Discovery,Pharmacology,General Medicine

Link

http://journals.sagepub.com/doi/pdf/10.1177/1934578X1501000674

Reference49 articles.

1. The Stemona Alkaloids

2. Stemona Alkaloids: Biosynthesis, Classification, and Biogenetic Relationships

3. Recent progress in the chemistry of the Stemona alkaloids

4. The chemistry of Stemona alkaloids: An update

5. Structural Relationships, Distribution and Biological Activities ofStemonaAlkaloids

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1. Reductive Oxy-Nazarov Cyclization toward Expedient Construction of a Cyclopenta[1,2-b]pyrrolo[1,2-a]azepine Ring System: Formal Total Syntheses of Stemonamine and Cephalotaxine;The Journal of Organic Chemistry;2024-03-27

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4. Exploring Cyclization Strategies to Access Stemona Alkaloids: Subtle Effects Influencing Reactivity in Intramolecular Michael Additions;Organic Letters;2021-10-22

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