Controllable skeletal reorganizations in natural product synthesis-Reference-Cited by-同舟云学术

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Controllable skeletal reorganizations in natural product synthesis

Published:2024 Issue:2 Volume:41 Page:251-272
ISSN:0265-0568
Container-title:Natural Product Reports
language:en
Short-container-title:Nat. Prod. Rep.

Author:

Zhang Zeliang¹^ORCID,Qian Xiao¹^ORCID,Gu Yucheng²^ORCID,Gui Jinghan¹^ORCID

Affiliation:

1. State Key Laboratory of Chemical Biology, Shanghai Institute of Organic Chemistry, University of Chinese Academy of Sciences, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032, China

2. Syngenta, Jealott's Hill International Research Centre, Bracknell, Berkshire RG42 6EY, UK

Abstract

This review highlights controllable skeletal reorganization, which involves the formation, cleavage, and migration of C–C and C–heteroatom bonds, as a powerful strategy in the efficient syntheses of steroid, terpenoid and alkaloid natural products.

Funder

National Key Research and Development Program of China

Science and Technology Commission of Shanghai Municipality

National Natural Science Foundation of China

Chinese Academy of Sciences

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/NP/D3NP00066D

Reference210 articles.

1. General methods of synthetic analysis. Strategic bond disconnections for bridged polycyclic structures

2. The Art and Science of Total Synthesis at the Dawn of the Twenty-First Century

3. Synthesis at the molecular frontier

4. Aiming for the Ideal Synthesis

5. Natural Product Synthesis: Changes over Time

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1. Bioinspired Total Synthesis of 3-epi-Junipercedrol;Organic Letters;2024-08-27

2. Natural products reverse cisplatin resistance in the hypoxic tumor microenvironment;Cancer Letters;2024-08

3. Rapid Access to Tigliane, Ingenane, and Rhamnofolane Diterpenes from a Lathyrane Precursor via Biomimetic Skeleton Transformation Strategy;Journal of Natural Products;2024-05-10

4. Recent developments in the enzymatic modifications of steroid scaffolds;Organic & Biomolecular Chemistry;2024

5. Strategic convergent synthesis en route to Veratrum steroidal alkaloids;Organic Chemistry Frontiers;2024

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