Highly chemoselective intermolecular cross-benzoin reactions using an ad hoc designed novel N-heterocyclic carbene catalyst-Reference-Cited by-同舟云学术

Highly chemoselective intermolecular cross-benzoin reactions using an ad hoc designed novel N-heterocyclic carbene catalyst

Published:2018 Issue:5 Volume:16 Page:780-786
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Delany Eoghan G.¹²³⁴^ORCID,Connon Stephen J.¹²³⁴^ORCID

Affiliation:

1. School of Chemistry Trinity Biomedical Sciences Institute

2. Trinity College Dublin

3. Dublin 2

4. Ireland

Abstract

A new N-heterocyclic carbene catalyst incorporating a bulky yet electron-deficient N-aryl substituent promotes highly chemoselective intermolecular crossed benzoin condensations.

Funder

Irish Research Council

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2018/OB/C7OB03005C

Reference50 articles.

1. Untersuchungen über das Radikal der Benzoesäure

2. Biocatalytic Strategies for the Asymmetric Synthesis of α-Hydroxy Ketones

3. Enhanced production of R-phenylacetylcarbinol (R-PAC) through enzymatic biotransformation

4. Carbene Catalysts

5. Lessons from Nature: Biomimetic Organocatalytic Carbon−Carbon Bond Formations

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