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Chemical name: (S)-2-Azido-6-[(4-methyltrityl)amino]hexanoic acid // Synonyms: N3-Lys(Mtt)-OH, alpha-Azido-N-epsilon-p-metyltrityl-L-lysine
|Molecular weight:||428,53 g/mol|
Update 1 of: alpha,beta-Diamino Acids: Biological Significance and Synthetic Approaches; Alma Viso, Roberto Fernndez de la Pradilla, Mariola Tortosa, Ana Garca, and Aida Flores; Chem. Rev. 2011; 111: PR1-PR42. DOI 10.1021/cr100127y.
Orthogonally Protected Cyclo--tertapeptides as Solid-Supported Scaffolds for the Synthesis of Glycoclusters; Pasi Virta, Marika Karskela, Harri Lnnberg; J.Org.Chem 2006; 71: 1989-1999.
Stereocontrolled Route to Vicinal Diamines by [3.3] Sigmatropic Rearrangement of Allyl Cyanate: Asymmetric Synthesis of anti-(2R,3R)-and syn-(2R,3S)-2,3-Diaminobutanoic Acids; Yoshiyasu Ichikawa, Haruka Egawa, Takashi Ito, Minoru Isobe, Keiji Nakano, and Hiyoshizo Kotsuki; Org.Lett. 2006; 8(25): 5737-5740.
Efficient Synthesis of orthogonally protected ant-2,3-diamino acids; Stefania Capone, Annalisa Guaregna, Giovanni Palumbo, Silvana Pedatella; Tetrahedron 2005; 61: 6575-6579.
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