Synthesis of Nitrogen Heterocycles by Intramolecular Michael Type of Amination via Reduction of Imines with Di-n-butyliodotin Hydride (n-Bu2SnIH)

Novel nitrogen heterocycles were prepared by a one-pot procedure involving the reductive amination of the bifunctional substrates containing an aldehyde and enone groups with di-n-butyliodotin hydride (n-Bu2SnIH).

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Published in:Organic letters 1999-11, Vol.1 (10), p.1579-1581
Main Authors: Suwa, Toshihiro, Shibata, Ikuya, Nishino, Keita, Baba, Akio
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Language:English
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cited_by cdi_FETCH-LOGICAL-a257t-dbdb92ded910f67efe5724535bb85f47ece74d0d1288117b8a89ec712892f2783
cites cdi_FETCH-LOGICAL-a257t-dbdb92ded910f67efe5724535bb85f47ece74d0d1288117b8a89ec712892f2783
container_end_page 1581
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container_title Organic letters
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creator Suwa, Toshihiro
Shibata, Ikuya
Nishino, Keita
Baba, Akio
description Novel nitrogen heterocycles were prepared by a one-pot procedure involving the reductive amination of the bifunctional substrates containing an aldehyde and enone groups with di-n-butyliodotin hydride (n-Bu2SnIH).
doi_str_mv 10.1021/ol990225i
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title Synthesis of Nitrogen Heterocycles by Intramolecular Michael Type of Amination via Reduction of Imines with Di-n-butyliodotin Hydride (n-Bu2SnIH)
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