Selectively Protected Chiral 1,2,4-Triaminobutanes and Chiral Vicinal 1,2-Diamines

DOI: 10.1016/S0957-4166(00)86240-0

Source and publish data:

Tetrahedron Asymmetry p. 887 - 894 (1994)

Update date:2022-08-05

Topics: Chiral 1,2-Diamines Vicinal Selectively Protected

Authors:

Altman, Janina

Ben-Ishai, Dov

Beck, Wolfgang

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Article abstract of DOI:10.1016/S0957-4166(00)86240-0

Stepwise t-butoxycarbonylation of (S)-5-aminomethyl-2-pyrrolidone to mono-, di- and triacylated compounds has been elaborated.Ring opening of (S)-5-(Boc-aminomethyl)-N¹-Boc-2-pyrrolidone with LiOH afforded the Boc-protected 4,5-diaminovaleric a

Full text of DOI:10.1016/S0957-4166(00)86240-0

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Product name:(S)-N¹,N²-dibenzyloxycarbonyl-N⁴-t-butoxycarbonyl-1,2,4-triaminobutane

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