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A Cyclobutanol Ring-Expansion Approach to Oxygenated Carbazoles: Total Synthesis of Glycoborine, Carbazomycin A and Carbazomycin B
被引:7
|作者:
Natho, Philipp
[1
]
Allen, Lewis A. T.
[1
]
Parsons, Philip J.
[1
]
机构:
[1] Imperial Coll London, Dept Chem, London W12 0BZ, England
来源:
基金:
英国工程与自然科学研究理事会;
关键词:
total synthesis;
ring expansion;
cyclization;
antifungal agents;
rearrangement;
ALKALOIDS CARBAZOMYCIN;
ORGANIC-SYNTHESIS;
AMINATION;
IDENTIFICATION;
ANTIBIOTICS;
COMPLEXES;
ROOTS;
ROUTE;
D O I:
10.1055/s-0042-1751411
中图分类号:
O62 [有机化学];
学科分类号:
070303 ;
081704 ;
摘要:
The transition-metal-free total syntheses of the oxygenated carbazole natural products glycoborine, carbazomycin A and carbazomycin B are reported. The key step involves an NBS-mediated cyclobutanol ring expansion to 4-tetralones for the preparation of the tricyclic carbazole core.
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页码:937 / 942
页数:6
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