Stereoselective Synthesis of Highly Functionalized 5- and 6-Membered Aminocyclitols Starting with a Readily Available
Raghavendra Achary1, Hyeong Rae Kim1,2, Hyeon-Kyu Lee1,2
1Korea Chemical Bank , Korea Research Institute of Chemical Technology , P.O. Box 107, Yuseong, Daejeon 305-600 , Korea.
The Journal of Organic Chemistry
|March 15, 2019
Abstract:
Stereoselective transformations of 4-vinyl-2-azetidinone derivative 4 into a variety of highly functionalized 6- and 5-membered carbocyclic compounds 7 and 9 were carried out using sequences involving sequential C1-N bond cleavage and Ru-catalyzed ring-closing metathesis. The derived carbocycles were further transformed into polyhydroxylated 6- and 5-membered aminocyclitols.
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