Asymmetric aziridination by reaction of chiral sulfinimine derived from (+)-camphor with dimethyloxosulfonium methylide

Article abstract of DOI:10.1080/00397910008087125

Addition of dimethyloxosulfonium methylide to chiral nonracemic pure (+)-camphor-derived sulfinimine I affords N-sulfinyl aziridine, which are easily separated. The N-(+)-camphor-based-sulfinyl auxiliary, was removed without ring opening by treatment with

Full text of DOI:10.1080/00397910008087125

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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Asymmetric Aziridination by
Reaction of Chiral Sulfinimine
Derived From (+)-Camphor
with Dimethyloxosulfonium
Methylide
a
a
a
a
Wei Zhu , Yan Li , Zhiyong Chen , Di Li
&
a
Guishu Yang
a
Chengdu Institute of Organic Chemistry, Chinese
Academy of Sciences, Chengdu, 610041, P. R. China
Published online: 04 Dec 2007.
To cite this article: Wei Zhu , Yan Li , Zhiyong Chen , Di Li & Guishu Yang (2000)
Asymmetric Aziridination by Reaction of Chiral Sulfinimine Derived From (+)-Camphor
with Dimethyloxosulfonium Methylide, Synthetic Communications: An International
Journal for Rapid Communication of Synthetic Organic Chemistry, 30:6, 1075-1081,
DOI: 10.1080/00397910008087125
To link to this article: http://dx.doi.org/10.1080/00397910008087125
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