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Transition metal complexes in organic synthesis, part 38. First total synthesis of carbazomycin G and H
The first total synthesis of the carbazole quinol alkaloids carbazomycin G and H has been achieved by a highly convergent synthesis using an iron-mediated construction of the carbazole nucleus as key-step. The first total synthesis of the carbazole quinol alkaloids carbazomycin G and H is described...
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Published in: | Tetrahedron letters 1997-06, Vol.38 (23), p.4051-4054 |
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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: | The first total synthesis of the carbazole quinol alkaloids carbazomycin G and H has been achieved by a highly convergent synthesis using an iron-mediated construction of the carbazole nucleus as key-step.
The first total synthesis of the carbazole quinol alkaloids carbazomycin G and H is described by a convergent iron-mediated construction of the carbazole nucleus starting with the complexes
1a,
1b, and the arylamine
2 as precursors. |
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ISSN: | 0040-4039 1873-3581 |
DOI: | 10.1016/S0040-4039(97)00826-5 |