128414-07-3

Basic information

• Product Name: (-)-tert-butyl (2S,3R,4R)-3,4-dihydroxy-1,6-diphenylhexan-2-ylcarbamate
• Synonyms: (-)-tert-butyl (2S,3R,4R)-3,4-dihydroxy-1,6-diphenylhexan-2-ylcarbamate
• CAS NO: 128414-07-3
• Molecular Weight: 385.503
• Mol File: 128414-07-3.mol

Chemical Properties

• CAS DataBase Reference: (-)-tert-butyl (2S,3R,4R)-3,4-dihydroxy-1,6-diphenylhexan-2-ylcarbamate(CAS DataBase Reference)
• NIST Chemistry Reference: (-)-tert-butyl (2S,3R,4R)-3,4-dihydroxy-1,6-diphenylhexan-2-ylcarbamate(128414-07-3)
• EPA Substance Registry System: (-)-tert-butyl (2S,3R,4R)-3,4-dihydroxy-1,6-diphenylhexan-2-ylcarbamate(128414-07-3)

Safety Data

• Hazardous Substances Data: 128414-07-3(Hazardous Substances Data)

Upstream product

• 13734-34-4 N-tert-butoxycarbonyl-L-phenylalanine 
• 1312025-89-0 (-)-O-(3R,5S)-5-(tert-butoxycarbonyl)amino-4-oxo-1,6-diphenylhexan-3-yl pyrrolidine-1-carbothioate 
• 169140-88-9 (+)-(S)-O-3-phenyl-1-(tri-n-butylstannyl)propyl pyrrolidine-1-carbothioate 
• 1279668-23-3 (-)-(S)-S-4-nitrophenyl 2-(tert-butoxycarbonyl)amino-3-phenylpropanethioate 
• 104-53-0 3-phenyl-propionaldehyde 
• 72155-45-4 Boc-L-phenylalaninal 

Relevant articles and documents

Stereocontrolled synthesis of α-amino-α′-alkoxy ketones by a copper-catalyzed cross-coupling of peptidic thiol esters and α-alkoxyalkylstannanes

A stereocontrolled synthesis of α-amino-α′-alkoxy ketones is described. This pH-neutral copper(I) thiophene-2-carboxylate (CuTC)-catalyzed cross-coupling of amino acid thiol esters and chiral nonracemic α-alkoxyalkylstannanes gives α-amino-α′-alkoxy keton

Stereoselective Synthesis of 3-Amino 1,2-Diols via Intermolecular Pinacol Cross-Coupling of α-Aldehydes with Aliphatic Aldehydes. Short Asymmetric Syntheses of Two 2,3,6-Trideoxy-3-amino Sugars

syn,syn-3-Amino 1,2-diols are prepared via a pinacol cross coupling reaction between N-Cbz- or N-Boc-α-amino aldehydes and aliphatic aldehydes.Application of this methodology to the synthesis of two amino sugars starting from N-Cbz-L-aspartic acid are described.