ISSN:
0947-3440
Keywords:
4-Thiazolidinones
;
L-Menthone spiro acetals
;
Chemistry
;
Organic Chemistry
Source:
Wiley InterScience Backfile Collection 1832-2000
Topics:
Chemistry and Pharmacology
Notes:
By acetalisation of L-menthone (2) with mercaptoacetic acid and derivatives of benzylamine, the spirocyclic N,S-acetals 3 were obtained as single diastereomers. The reaction of an epimeric mixture of unsubstituted thiazolidinones 4 with acetic anhydride or allyl iodide afforded homochiral N-acetyl (5) or N-allyl N,S-acetals (6), respectively. The configuration of the new stereogenic centres were proven by X-ray crystallography.
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1002/jlac.1995199508193
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