133038-96-7

Basic information

• Product Name: [(2S,3S)-3-(Trityl-amino)-tetrahydro-furan-2-yl]-acetic acid
• CAS NO: 133038-96-7
• Molecular Weight: 387.478
• Mol File: 133038-96-7.mol

Chemical Properties

• CAS DataBase Reference: [(2S,3S)-3-(Trityl-amino)-tetrahydro-furan-2-yl]-acetic acid(CAS DataBase Reference)
• NIST Chemistry Reference: [(2S,3S)-3-(Trityl-amino)-tetrahydro-furan-2-yl]-acetic acid(133038-96-7)
• EPA Substance Registry System: [(2S,3S)-3-(Trityl-amino)-tetrahydro-furan-2-yl]-acetic acid(133038-96-7)

Safety Data

• Hazardous Substances Data: 133038-96-7(Hazardous Substances Data)

Upstream product

• 133038-91-2 N-tritylhomoserine lactol 
• 133069-72-4 (S),(E)-6-hydroxy-4-(triphenylmethylamino)hex-2-enoic acid methyl ester 
• 21204-67-1 methyl (triphenylphosphoranylidene)acetate 
• 133038-93-4 methyl (2S,3S)-3-triphenylmethylaminooxolan-20ylacetate 

Relevant articles and documents

Total syntheses of novel dideoxynucleoside analogues using chiral amino acids

N-Tritylated L- and D-methionine and L-glutamic acid were used to obtain novel chiral iso-dideoxynucleoside analogues incorporating a tetrahydrofuranyl or a tetrahyropyranyl ring as the pseudosugar part, and at positions 2 and 3 of the ring an hydroxyethyl group and thymine or adenine, respectively. (C) 2000 Elsevier Science Ltd.

Synthesis of Conformationally Restricted Chiral γ-Aminobutyric Acid (GABA) Analogues

The epimeric (2S, 3S)- and (2R, 3S)-3-amino-2-(carboxymethyl)oxolanes have been synthesised from (S)-N-tritylhomoserine lactone.The lactone was first reduced with diisobutylaluminium hydride to a diastereomeric mixture of the corresponding lactols which u