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Structure of the product of the reaction of 3,6-dioxa-1,8-(di-2,3-dichloromaleimido)octane with 3,6-dioxaoctane-1,8-diamine

✍ Scribed by É. V. Ganin; Yu. A. Simonov; A. A. Dvorkin; G. S. Musienko; G. G. Shagas; T. I. Malinovskii


Publisher
Springer US
Year
1992
Tongue
English
Weight
338 KB
Volume
28
Category
Article
ISSN
0009-3122

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✍ Andrea Trabocchi; Gloria Menchi; Massimo Rolla; Fabrizio Machetti; Ilaria Bucell 📂 Article 📅 2003 🏛 Elsevier Science 🌐 French ⚖ 196 KB

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