On attempted oxidative cyclisation of isomeric N,N'-diphenylphenylenediamines and their N,N'-dimethyl derivatives by palladium(II) acetate and UV light

Article abstract of DOI:10.1080/00397910008086992

The cyclisation of N,N'-diphenyl-o-, m- and p-phenylenediamines and their N,N'-dimethyl derivatives by palladium(II) acetate and UV light separately led to both bis-cyclisation, furnishing indolocarbazoles, and mono-cyclisations with cleavage as well as retention of one substituent, producing substituted carbazoles.

Full text of DOI:10.1080/00397910008086992

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Synthetic Communications: An
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Organic Chemistry
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On Attempted Oxidative
Cyclisation of Isomeric N,N'-
Diphenylphenylenediamines
and Their N,N'-Dimethyl
Derivatives by Palladium(II)
Acetate and Uv Light
Manas Chakrabarty a , Archana Batabyal b & Shampa
Khasnobis c
a Dept. of Chemistry, Bose Institute, 93/1, A.P.C.
Road, Calcutta, 700009, India
b Dept. of Chemistry, St. Paul's College, Calcutta,
700009
c Dept. of Chemistry, A.J.C. Bose College, Calcutta,
700020, India
Published online: 04 Dec 2007.
To cite this article: Manas Chakrabarty , Archana Batabyal & Shampa
Khasnobis (2000) On Attempted Oxidative Cyclisation of Isomeric N,N'-
Diphenylphenylenediamines and Their N,N'-Dimethyl Derivatives by Palladium(II)
Acetate and Uv Light, Synthetic Communications: An International Journal for
Rapid Communication of Synthetic Organic Chemistry, 30:20, 3651-3668, DOI:
10.1080/00397910008086992
To link to this article: http://dx.doi.org/10.1080/00397910008086992

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