605668-35-7Relevant academic research and scientific papers
Synthesis of 4-aminomethyl-tetrahydrofuran-2-carboxylates with 2,4-cis and 2,4-trans relationships
Edwards, Alison A.,Sanjayan, Gangadharar J.,Hachisu, Shuji,Soengas, Raquel,Stewart, Alistair,Tranter, George E.,Fleet, George W.J.
, p. 4110 - 4119 (2006)
Templated tetrahydrofuran-based γ-azido esters were prepared with the C-2 and C-4 functionalities in cis and trans relative configurations. This was achieved by ring contraction of the suitably protected 2-O-triflates of pentono-1,5-lactones (d-ribose and
Templated scaffolds of cis- and trans-tetrahydrofuran γ-amino acids: γ-azido-β-hydroxy-tetrahydrofuran-2-carboxylates from pentono-δ-lactones
Sanjayan, Gangadharar J.,Stewart, Alistair,Hachisu, Shuji,Gonzalez, Raquel,Watterson, Mark P.,Fleet, George W.J.
, p. 5847 - 5851 (2007/10/03)
Short syntheses of enantiomeric templated scaffolds of cis- and trans-tetrahydrofuran γ-amino acids from pentono-δ-lactones derived from arabinose and ribose are reported; an unexpectedly efficient synthesis of a templated tetrahydrofuran β-amino acid by
