Asymmetric synthesis of trans-4,5-disubstituted γ-butyrolactones involving a key allylboration step. First access to (−)-nicotlactone B and (−)-galbacin-Reference-Cited by-同舟云学术

Asymmetric synthesis of trans-4,5-disubstituted γ-butyrolactones involving a key allylboration step. First access to (−)-nicotlactone B and (−)-galbacin

Published:2018 Issue:10 Volume:16 Page:1672-1678
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Henrion S.¹²³⁴⁵,Macé A.¹²³⁴⁵,Vallejos M. M.⁶⁷⁸⁹,Roisnel T.¹²³⁴⁵,Carboni B.¹²³⁴⁵,Villalgordo J. M.¹⁰¹¹¹²¹³¹⁴,Carreaux F.¹²³⁴⁵^ORCID

Affiliation:

1. Univ Rennes

2. CNRS

3. ISCR (Institut des Sciences Chimiques de Rennes) – UMR 6226

4. F-35000 Rennes

5. France

6. Laboratorio de QuÍmÍca Organica. Universidad Nacional del Nordeste. CONICET

7. FACENA

8. Corrientes

9. Argentina

10. VillaPharma Research

11. Parque Tecnológico de Fuente Alamo

12. Ctra El Estrecho-Lobosillo

13. 30320 Murcia

14. Spain

Abstract

A new approach based on one-pot sequential transformations with application for the first total synthesis of (−)-nicotlactone B and (−)-galbacin.

Funder

Université de Rennes 1

Centre National de la Recherche Scientifique

Consejo Nacional de Investigaciones Científicas y Técnicas

Agencia Nacional de Promoción Científica y Tecnológica

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2018/OB/C8OB00101D

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2. Synthetic approaches towards structurally diverse γ-butyrolactone natural-product-like compounds

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5. First enantioselective synthesis of (−)-talaumidin, a neurotrophic diaryltetrahydrofuran-type lignan

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