78907-33-2Relevant academic research and scientific papers
An expeditious approach to tri-substituted chiral thiazolines
Abdel-Jalil, Raid J.,Saeed, Muhammad,Voelter, Wolfgang
, p. 2435 - 2437 (2001)
A regio- and stereoselective route from the cis-oriented epoxytriflate pentoses 1 and 4 via 4-amino-4-deoxy sugars 2 and 5 to chiral thiazoline derivatives 3a-e and 6a-e in high yields is described.
A Convenient Synthesis of 4-Amino-4-desoxy Sugars
Malik, Abdul,Roosz, Michael,Voelter, Wolfgang
, p. 559 - 561 (2007/10/02)
Displacement of the triflyl by the amino group in benzyl-2,3-anhydro-4-triflyl-pyranosides 4-6 gives with inversion the benzyl-2,3-anhydro-4-amino-4-desoxypyranosides 7-9.The triflyl group turns out to be a reactive leaving group which can be replaced by
A New Efficient Access to Aminodeoxy Sugars
Malik, Abdul,Afza, Nighat,Roosz, Michael,Voelter, Wolfgang
, p. 1530 - 1531 (2007/10/02)
A mild and convenient synthesis of aminodeoxy sugars is described, involving the esterification of partially protected carbohydrates with trifluoromethanesulphonic anhydride and the reaction of the resulting trifluoromethanesulphonates with ammonia; the d
SYNTHESIS AND BIOLOGICAL ACTIVITES OF 4-(D-ALANYLAMINO)-2-AMINO-2,3,4-TRIDEOXY-L-THREO-PENTOSE (3-DEOXYPRUMYCIN)
Hashimoto, Hironobu,Koichi, Araki,Miazawa, Ken-Ichi,Yoshimura, Juji
, p. 59 - 69 (2007/10/02)
Three analogs of prumycin , i.e., the 3-deoxygenated (1), that having the 2-amino and 3-hydroxyl groups interchanged (2), and that having C-2 deaminated (3), were synthesized.Examination of the antifunga
C-4-Triflate Displacement by Azide in 2,3-Anhydro Sugars; a New Way to 4-Amino-4-deoxy Sugars
Kimmich, Reinhard,Voelter, Wolfgang
, p. 1100 - 1104 (2007/10/02)
Displacement of the triflyl by the azido group in benzyl-2,3-anhydro-4-triflyl-α-D-pyranosides 4-6 gives with inversion the benzyl-2,3-anhydro-4-azido-4-deoxypyranosides 7-9.The triflyl group turns out to be a reactive leaving group which can be replaced
