1,2-RADICAL REARRANGEMENTS OF ARYL, FURANYL AND THIOPHENYL GROUPS FROM CARBON TO NITROGEN

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1,2-Radical rearrangements of aryl, furanyl and thiophenyl groups from carbon to nitrogen using azido groups as radical precursors are observed for the first time; the 1,2-aryl rearrangement is applied to the synthesis of phenanthridine derivatives from 6-fluorenyl azides.
Publisher
ROYAL SOC CHEMISTRY
Issue Date
1995-08
Language
English
Article Type
Article
Keywords

NEOPHYL REARRANGEMENT; RING EXPANSION; RADICALS

Citation

JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, pp.1607 - 1608

ISSN
0022-4936
URI
http://hdl.handle.net/10203/67744
Appears in Collection
CH-Journal Papers(저널논문)
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