Journal
DALTON TRANSACTIONS
Volume 47, Issue 7, Pages 2453-2459Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c7dt04751g
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Funding
- National Natural Sciences Foundation of China [21372245, 21772223]
- CAS-Croucher Funding Scheme
- NSFC/RGC Joint Research Scheme [N_CUHK442/14]
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A variety of carborane-fused carbo- and heterocycles were prepared in good to high isolated yields via the reaction of carborane-fused zirconacyclopentane with a series of substrates such as S-8, Se, Te, CO, XylNC, MeOOC-CH=N-2, PhPCl2, (Bu2SnCl2)-Bu-n and Me2GeCl2. However, it was found that the Zr-C bond in the zirconacyclopentane did not show any reactivity towards PhBCl2, PhCN and PhCH-NPh. This approach represents a promising route to functionalized carboranes that are difficult to access by conventional methods.
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