242805-31-8Relevant articles and documents
An abnormal deallylation reaction of an L-fucopyranoside
Li, Zhong-Jun,Li, Hui,Lu, Yi-Ping,Shi, Xu-Ling,Cai, Meng-Shen
, p. 191 - 192 (1999)
Deallylation of allyl 2,3,4-tri-O-benzyl-L-fucopyranoside in the presence of palladium chloride and cuprous chloride led to an unexpected result. Instead of the expected deallylated product, (2-oxopropyl)-2,3,4-tri-O-benzyl-L-fucopyranoside was obtained.
Synthesis of new [(2S)-N-(p-Tolylsulfonyl)-2-Pyrrolidinyl]Propyl 2,3,4-Tri-O-Acetyl- and 2,3,4-Tri-O-Benzyl-β-L-Fucopyranosides
E Silva, Maria Joselice,Srivastava, Rajendra M.,Doboszewski, Bogdan,Cottier, Louis,Sinou, Denis
scheme or table, p. 105 - 111 (2011/06/26)
Synthesis of two new glycoheterocyclic compounds, [(2S)-N-(p-tolylsulfonyl) -2-pyrrolidinyl]propyl 2,3,4-tri-O-acetyl- and 2,3,4-tri-O-benzyl-β-L- fucopyranosides la and lb, starting from δ-amino alcohol (-)-[(2S)-N-(ptolylsulfonyl)-2-pyrrolidinyl]propan-l-ol 2 and O-α-L-fucosyltrichloroacetimidates 3a or 3b as glycosyl donor is described. Hitherto δ-aminoalcohol 2 was synthesized from L-proline without any racemization during its preparation.