Recent asymmetric synthesis of natural products bearing an α-tertiary amine moiety <i>via</i> temporary chirality induction strategies-Reference-Cited by-同舟云学术

Recent asymmetric synthesis of natural products bearing an α-tertiary amine moiety via temporary chirality induction strategies

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

Author:

Jeon Hongjun¹^ORCID,Kim Jae Hyun²^ORCID,Kim Sanghee³^ORCID

Affiliation:

1. Therapeutics & Biotechnology Division, Korea Research Institute of Chemical Technology (KRICT), Daejeon 34114, Republic of Korea

2. College of Pharmacy, Chung-Ang University, Seoul 06974, Republic of Korea

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

Abstract

This review highlights recent advances in the asymmetric synthesis of α-tertiary amine natural products via temporary chirality induction methods: Seebach's self-regeneration of stereocenters, C-to-N-to-C chirality transfer, and memory of chirality.

Funder

National Research Foundation of Korea

Korea Research Institute of Chemical Technology

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2024/NP/D3NP00032J

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