Construction of stereogenic center beta to the N-Pyrrolidinyl moiety via diastereoselective reactions of tricyclic lactones and the synthesis of (−)-Indolizidine 195G-Reference-Cited by-同舟云学术

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Construction of stereogenic center beta to the N-Pyrrolidinyl moiety via diastereoselective reactions of tricyclic lactones and the synthesis of (−)-Indolizidine 195G

Published:2024-06 Issue: Volume:159 Page:134024
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Huang Rou-Jie,Luo Ching-Zong,Liao Wei-Kai,Chuang Hsiang-Yu,Li Yu-Jang

Funder

Ministry of Science and Technology, Taiwan

National Chung-Hsing University

National Science and Technology Council

Publisher

Elsevier BV

Reference35 articles.

1. Stereoselective synthesis of the densely functionalized C1–C9 fragment of amphidinolides C and F

2. Synthesis of Enantiomerically Pure (−)-Wine Lactone Based on a Palladium-Catalyzed Enantioselective Allylic Substitution

3. Evaluation of the Claisen rearrangement of 2-cyclohexenols for the stereoselective construction of a terpene synthon

4. Asymmetric [3,3]- and [1,3]-Sigmatropic Rearrangements of γ-Allyloxy Vinylogous Urethanes

5. NOEs of 12 & 13 See; Electronic Supplementary Material, page S44..

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