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An intramolecular, Ni(0)-mediated approach to the nonracemic biaryl portion of vancomycin
Using a tether derived from tartaric acid to which is attached two halogenated phenylglycine residues, a Ni(0)-induced biaryl coupling can be effected with complete control of axial chirality. Use of a nonracemic tether to induce S-axial chirality.
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Published in: | Tetrahedron letters 1999-05, Vol.40 (19), p.3677-3680 |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Using a tether derived from tartaric acid to which is attached two halogenated phenylglycine residues, a Ni(0)-induced biaryl coupling can be effected with complete control of axial chirality.
Use of a nonracemic tether to induce
S-axial chirality. |
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ISSN: | 0040-4039 1873-3581 |
DOI: | 10.1016/S0040-4039(99)00557-2 |