Rh(II)-catalyzed enantioselective synthesis of acuminatin through a C–H insertion reaction of a non-stabilized carbenoid-Reference-Cited by-同舟云学术

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Rh(II)-catalyzed enantioselective synthesis of acuminatin through a C–H insertion reaction of a non-stabilized carbenoid

Published:2013-07 Issue:26 Volume:69 Page:5511-5516
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

López-Sánchez Cristóbal,Álvarez-Corral Míriam,Jiménez-González Leticia,Muñoz-Dorado Manuel,Rodríguez-García Ignacio

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference57 articles.

1. Lignans and neolignans as lead compounds

2. Acuminatin, a new bis-phenylpropide from Magnolia acuminata L.

3. Direct characterization of nutmeg constituents by mass spectrometry-mass spectrometry

4. Simple Synthesis of Benzofuranoid Neolignans from Myristica fragrans

5. Neolignans from fruits of Virola pavonis

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1. Palladium/Xu‐Phos Catalyzed Enantioselective Intramolecular Heck Reaction of Unactivated Alkenes;Chinese Journal of Chemistry;2024-06-10

2. Heterocycles from Donor and Donor/Donor Carbenes;Topics in Heterocyclic Chemistry;2023

3. Recent advances in transition-metal-catalyzed carbene insertion to C–H bonds;Chemical Society Reviews;2022

4. 1H and 13C NMR Spectral Data of Neolignans Isolated from Piper Species;Current Organic Chemistry;2020-10-13

5. Recent progress on donor and donor–donor carbenes;Chemical Society Reviews;2020

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