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Journal article

Synthesis of (+)-nocardione A--use of formal radical cyclization onto a benzene ring.

Abstract:
Juglone (7) was converted into enone 13; this underwent radical cyclization to afford 15, which was aromatized to 16 and elaborated into (+)-nocardione A (1), the enantiomer of the naturally-occurring tyrosine phosphatase inhibitor (-)-nocardione A (2).
Publication status:
Published

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Publisher copy:
10.1039/b307937f

Authors


Journal:
Chemical communications (Cambridge, England)
Volume:
9
Issue:
19
Pages:
2464-2465
Publication date:
2003-10-05
DOI:
EISSN:
1364-548X
ISSN:
1359-7345
URN:
uuid:9a6162ad-2d65-402d-8ddc-3badaf435417
Source identifiers:
117856
Local pid:
pubs:117856

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