Open Access Repository

Borane-catalyzed stereoselective C–H Insertion, cyclopropanation, and ring-opening reactions

Dasgupta, A, Babaahmadi, R, Slater, B, Yates, BF ORCID: 0000-0001-9663-3301, Ariafard, A ORCID: 0000-0003-2383-6380 and Melen, RL 2020 , 'Borane-catalyzed stereoselective C–H Insertion, cyclopropanation, and ring-opening reactions' , Chem, vol. 6, no. 9 , pp. 2364-2381 , doi: 10.1016/j.chempr.2020.06.035.

Full text not available from this repository.


Lewis acidic boranes have been shown to be effective metal-free catalysts for highly selective reactions of donor-acceptor diazo compounds to a range of substrates. The reactions of α-aryl α-diazoesters with nitrogen heterocycles indole or pyrrole selectively generate C3 and C2 C–H insertion products, respectively, in good to excellent yields even when using unprotected indoles. Alternatively, benzofuran, indene, and alkene substrates give exclusively cyclopropanated products with α-aryl α-diazoesters, whereas the reactions with furans lead to ring-opening. Comprehensive theoretical calculations have been used to explain the differing reactivities and high selectivities of these reactions. Overall, this work demonstrates the selective metal-free catalytic reactions of α-aryl α-diazoesters with (hetero)cycles and alkenes. This simple, mild reaction protocol represents an alternative to the commonly used precious metal systems and may provide future applications in the generation of biologically active compounds.

Item Type: Article
Authors/Creators:Dasgupta, A and Babaahmadi, R and Slater, B and Yates, BF and Ariafard, A and Melen, RL
Keywords: DFT analysis, cyclopropanation, C–H activation, borane catalysis, ring- opening reactions
Journal or Publication Title: Chem
Publisher: Cell Press
ISSN: 2451-9308
DOI / ID Number: 10.1016/j.chempr.2020.06.035
Related URLs:
Item Statistics: View statistics for this item

Actions (login required)

Item Control Page Item Control Page