2n Framework Electron Clusters: Directed Synthesis of Octachlorooctaborane, B8Cl8. The Activation of CH Bonds

DOI: 10.1021/ja00388a057

Source and publish data:

Journal of the American Chemical Society p. 6790 - 6791 (1982)

Update date:2022-07-30

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Authors:

Emery, S. L.

Morrison, J. A.

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Article abstract of DOI:10.1021/ja00388a057

Full text of DOI:10.1021/ja00388a057

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Article Doi

2n Framework Electron Clusters: Directed Synthesis of Octachlorooctaborane, B8Cl8. The Activation of CH Bonds

DOI: 10.1021/ja00388a057

Source and publish data:

Authors:

Article abstract of DOI:10.1021/ja00388a057

Full text of DOI:10.1021/ja00388a057

Products guided by the article

R&D Labs maybe for 83416-58-4

Relevant to this article

On cardioactive steroids. XII. The synthesis of (natural) bufalin and α'-isobufalin

A NEW SYNTHETIC METHOD OF 3-ACYLTETRONIC ACID DERIVATIVES AND ITS APPLICATION TO THE SYNTHESIS OF ISOASPERTETRONIN A(ISOGREGATIN A)

SYNTHESIS OF THE p-TOLUENESULFONATE OF OLEYL ALCOHOL UNDER CONDITIONS OF PHASE TRANSFER CATALYSIS

Electrochemical Reduction in the Synthesis of Catechol-Derived Peptides as Potential Metal Chelators and Enzyme Inhibitors

Isozeaxanthine: Chiralitaet und enantioselektive Synthese von (4R,4'R)-Isozeaxanthin((-)-(4R,4R')-β,β-Carotin-4,4'-diol)

Crystal structure, DFT, spectroscopic and biological activity evaluation of analgin complexes with Co(ii), Ni(ii) and Cu(ii)