Application of 2,3-aziridino-γ-lactone methodology toward the enantiospecific synthesis of the (3S,4S)-isomer of dihydroxy-L-glutamic acid
摘要:
The formal synthesis of benzyl 2,3-aziridino-N-(benzyloxycarbonyl)-2,3-dideoxy-γ-butyrolactone (21) from D-ribose is described. Reaction of 21 with excess benzyl alcohol in the presence of boron trifluoride etherate and hydrogenolysis of the product gave (3S,4S)-dihydroxy-L-glutamic acid ((3S,4S)-3).
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DOI:
10.1016/S0040-4020(99)00405-6
被引量:
年份:
1999
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2003
被引量:14
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