AI Article Synopsis
- An alkoxyallenyl zinc reagent reacts with benzyl imines from lactic and mandelic acids.
- The reaction exhibits high diastereoselectivity, producing specific stereochemical configurations.
- The result is the formation of 2-amino-1,3-diol derivatives featuring an anti-anti stereochemical arrangement.
Article Abstract
[see reaction]. 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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| http://dx.doi.org/10.1021/ol015941a | DOI Listing |
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