A convergent one-pot synthesis of secondary amines via aza-Wittig reaction

Article abstract of DOI:10.1080/00397919208021323

Secondary amines are obtained in moderate-good yields by reduction of crude imines prepared from N-alkyltriethoxyiminophosphoranes and aldehydes via the aza-Wittig reaction. N-Alkyltriethoxyiminophosphoranes are synthesized by one-pot azidation of alkyl bromides followed by Staudinger reaction.

Full text of DOI:10.1080/00397919208021323

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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A Convergent One-Pot
Synthesis of Secondary Amines
via Aza-Wittig Reaction
Tadeusz Gajda a , Anna Koziara a , Krystyna
Osowska-Pacewicka a , Stefan Zawadzki a & Andrzej
Zwierzak a
a Institute of Organic Chemistry, Technical
University, 2wirki 36, 90-924, Lodz, 40, Poland
Published online: 23 Sep 2006.
To cite this article: Tadeusz Gajda , Anna Koziara , Krystyna Osowska-Pacewicka ,
Stefan Zawadzki & Andrzej Zwierzak (1992): A Convergent One-Pot Synthesis
of Secondary Amines via Aza-Wittig Reaction, Synthetic Communications: An
International Journal for Rapid Communication of Synthetic Organic Chemistry, 22:13,
1929-1938
To link to this article: http://dx.doi.org/10.1080/00397919208021323
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