Affiliation:
1. EaStCHEM School of Chemistry, The University of Edinburgh
2. Medicinal Chemistry, Early Oncology, AstraZeneca
3. Pharmaceutical Technology & Development, Chemical Development U.K., AstraZeneca
Abstract
AbstractThis review highlights transborylation (controlled boron-boron exchange) and its applications as a turnover strategy in boron-catalysed methodologies. Catalytic applications of B–C, B–O, B–N, B–F, B–S, and B–Se transborylations are discussed in the context of transborylation-enabled catalysis, across a wide range of organic transformations including hydroboration, C–C bond formation, C–H borylation, chemoselective reduction, and asymmetric reduction.1 Introduction2 B–C Transborylation3 B–O Transborylation4 B–N Transborylation5 B–F Transborylation6 B–S Transborylation7 Conclusion
Funder
Royal Society
AstraZeneca
Engineering and Physical Sciences Research Council
Subject
Organic Chemistry,Catalysis
Cited by
3 articles.
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