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73Ge NMR spectra of 1,3-dioxa-6-aza-2-germacyclooctanes

✍ Scribed by E. Kupče; E. Lukevics; O.D. Flid; N.A. Viktorov; T.K. Gar


Publisher
Elsevier Science
Year
1989
Tongue
English
Weight
134 KB
Volume
372
Category
Article
ISSN
0022-328X

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New methodology for the synthesis of enantiopure 3-aza-6,8-dioxa-bicyclo[3.2.1]octane-carboxylic acids belonging to 7-endo-BTAa sub-class of g/d amino acids is described. The novelty is the use of 2,3-O-isopropylidene-erythrose instead of meso-tartaric acid derivative, thus allowing us to perform an