A Configurationally Stable Alkoxy
Allenyl Zinc Reagent, en Route to
anti-anti Vicinal Amino Diols

Normant, Jean F.

A Configurationally Stable Alkoxy Allenyl Zinc Reagent, en Route to anti-anti Vicinal Amino Diols

Posted on 2001-05-12 - 00:00

The reaction of an alkoxyallenyl zinc reagent with benzyl imines derived from lactic and mandelic acids proceeds highly diastereoselectively and leads to 2-amino-1,3-diol derivatives with an anti-anti pattern.

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Poisson, Jean-François; Normant, Jean F. (2016). A Configurationally Stable Alkoxy Allenyl Zinc Reagent, en Route to anti-anti Vicinal Amino Diols. ACS Publications. Collection. https://doi.org/10.1021/ol015941a

https://doi.org/10.1021/ol015941a

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A Configurationally Stable Alkoxy Allenyl Zinc Reagent, en Route to anti-anti Vicinal Amino Diols

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