Highly diastereoselective approach to novel tetrahydrofuran-fused indolizidinols: a one-step formation of three contiguous stereocenters-Reference-Cited by-同舟云学术

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Highly diastereoselective approach to novel tetrahydrofuran-fused indolizidinols: a one-step formation of three contiguous stereocenters

Published:2008-03 Issue:4 Volume:19 Page:467-475
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Šafář Peter,Žúžiová Jozefína,Bobošíková Mária,Marchalín Štefan,Prónayová Nadežda,Dalla Vincent,Daïch Adam

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference51 articles.

1. Development and viability of bovine preplacentation embryos treated with swainsonine in vitro

2. Indolizidine and quinolizidine alkaloids

3. Indolizidine and quinolizidine alkaloids

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1. Asymmetric arene hydrogenation: towards sustainability and application;Chemical Society Reviews;2023

2. Smart and concise entry to chiral spiro[cyclopentane-indolizidine]-tetraol diastereomers as a new aza-spirocyclic framework;New Journal of Chemistry;2021

3. Synthesis and sequential diastereoselective incorporation of hydroxyl groups into hexahydrofuro[3,2-f]indolizin-7(2H)-one to give mono-, di- and tetra-hydroxyfuroindolizidines;Organic & Biomolecular Chemistry;2020

4. Substrate induced diastereoselective hydrogenation/reduction of arenes and heteroarenes;RSC Advances;2016

5. (±)-Homocrepidine A, a Pair of Anti-inflammatory Enantiomeric Octahydroindolizine Alkaloid Dimers from Dendrobium crepidatum;Journal of Natural Products;2015-12-28

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