Straightforward synthesis of chiral non-racemic α-boryl isocyanides
Author:
Affiliation:
1. Department of Life Sciences
2. Università degli Studi di Modena e Reggio Emilia
3. Modena
4. Italy
5. International Doctorate School in Clinical and Experimental Medicine (CEM)
Abstract
A concise synthesis of chiral non-racemic α-boryl isocyanides is achieved. α-Ammonium boronates and N-formylamido boronic acid MIDA-esters were exploited as key intermediates.
Funder
Università Degli Studi di Modena e Reggio Emila
Fondazione Cassa di Risparmio di Modena
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2021/OB/D1OB00616A
Reference34 articles.
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2. Boronic acids: Preparation and Application in Organic Synthesis, Medicine and Materials , ed. D. G. Hall , Wiley , Weinheim , 2nd rev. edn, 2011
3. The versatility of boron in biological target engagement
4. .alpha.-Halo boronic esters: intermediates for stereodirected synthesis
5. Asymmetric synthesis with boronic esters
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1. Enantiopure β-isocyano-boronic esters: synthesis and exploitation in isocyanide-based multicomponent reactions;Molecular Diversity;2022-10-19
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