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Stereoselective synthesis of threo-3-hydroxycarboxylic acids. Stereocheminstry of an aldoltype addition under kinetic and thermodynamic control.

✍ Scribed by Johann Mulzer; Johann Segner; Gisela Brüntrup


Book ID
104235889
Publisher
Elsevier Science
Year
1977
Tongue
French
Weight
246 KB
Volume
18
Category
Article
ISSN
0040-4039

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✦ Synopsis


The addition of preformed enolates 1 to carbonyl compounds 2 results in the formation of metal chelates, which, having stereocenters at C-2 and C-5, are generally formed as mixtures of the threoand erythro-isomers 2 and 4'.