New economical, convenient procedures for the synthesis of catecholborane

dc.contributor.author Kanth, Josyula V.B.
dc.contributor.author Periasamy, Mariappan
dc.contributor.author Brown, Herbert C.
dc.date.accessioned 2022-03-27T09:10:09Z
dc.date.available 2022-03-27T09:10:09Z
dc.date.issued 2000-01-01
dc.description.abstract Catecholborane was conveniently synthesized by the reaction of tri-O-phenylene bis-borate (2) with diborane in triglyme or tetraglyme at moderate temperatures (70-80 °C). The product, catecholborane, can be distilled out in 85% yield with > 97% purity. The tri-O-phenylene bis-borate also reacts with borane-Lewis base complexes, such as BH3:DMS, BH3:THF, and BH3: NR3, with or without solvent, providing catecholborane of high purity in good yields.
dc.identifier.citation Organic Process Research and Development. v.4(6)
dc.identifier.issn 10836160
dc.identifier.uri 10.1021/op000291w
dc.identifier.uri https://pubs.acs.org/doi/10.1021/op000291w
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/12525
dc.title New economical, convenient procedures for the synthesis of catecholborane
dc.type Journal. Article
dspace.entity.type
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