Affiliation:
1. Department of Organic Chemistry Arrhenius Laboratory Stockholm University 10691 Stockholm Sweden
2. Department of Natural Sciences Mid Sweden University Holmgatan 10 85179 Sundsvall Sweden
3. Medicinal Chemistry, Research and Early Development Cardiovascular Renal and Metabolism (CVRM) BioPharmaceuticals R&D AstraZeneca Gothenburg 43183 Mölndal Sweden
Abstract
AbstractClassical Crabbé type SN2' substitutions of propargylic substrates has served as one of the standard methods for the synthesis of allenes. However, the stereospecific version of this transformation often requires either stoichiometric amounts of organocopper reagents or special functional groups on the substrates, and the chirality transfer efficiency is also capricious. Herein, we report a sustainable methodology for the synthesis of diverse 1,3‐di and tri‐substituted allenes by using a simple and cheap cellulose supported heterogeneous nanocopper catalyst (MCC‐Amp‐Cu(I/II)). This approach represents the first example of heterogeneous catalysis for the synthesis of chiral allenes. High yields and excellent enantiospecificity (up to 97 % yield, 99 % ee) were achieved for a wide range of di‐ and tri‐substituted allenes bearing various functional groups. It is worth noting that the applied heterogeneous catalyst could be recycled at least 5 times without any reduced reactivity. To demonstrate the synthetic utility of the developed protocol, we have applied it to the total synthesis of several chiral allenic natural products.
Subject
General Chemistry,Catalysis
Cited by
1 articles.
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