| Literature DB >> 26866576 |
Kirk W Shimkin1, Peter G Gildner1, Donald A Watson1.
Abstract
Copper catalysis now enables the efficient C-alkylation of nitroalkanes with α-bromonitriles. Using a simple and inexpensive catalyst, this process provides access to β-cyanonitroalkanes. The method is highly tolerant of various functional groups and substitution patterns. These functionally dense products serve as orthogonally masked 1,3-diamines, which can be revealed selectively for access to differentially substituted diamines. These products can also be exploited for the formation of complex cyanoalkenes and 5-aminoisoxazoles.Entities:
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Year: 2016 PMID: 26866576 PMCID: PMC4927086 DOI: 10.1021/acs.orglett.6b00093
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005