78907-33-2

Basic information

• Product Name: benzyl-2,3-anhydro-4-amino-4-desoxy-β-L-lyxopyranoside
• Synonyms: benzyl-2,3-anhydro-4-amino-4-desoxy-β-L-lyxopyranoside
• CAS NO: 78907-33-2
• Molecular Weight: 221.256
• Mol File: 78907-33-2.mol

Chemical Properties

• CAS DataBase Reference: benzyl-2,3-anhydro-4-amino-4-desoxy-β-L-lyxopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: benzyl-2,3-anhydro-4-amino-4-desoxy-β-L-lyxopyranoside(78907-33-2)
• EPA Substance Registry System: benzyl-2,3-anhydro-4-amino-4-desoxy-β-L-lyxopyranoside(78907-33-2)

Safety Data

• Hazardous Substances Data: 78907-33-2(Hazardous Substances Data)

Upstream product

• 62828-72-2 Benzyl-2,3-anhydro-4-azido-4-desoxy-β-L-lyxopyranosid 
• 61134-24-5 Benzyl 2,3-anhydro-α-D-ribopyranoside 
• 71204-44-9 benzyl 2,3-anhydro-4-O-trifluoromethanesulfonyl-α-D-ribopyranoside 

Downstream Products

• 81102-17-2 benzyl 4-(N-benzoyloxycarbonyl-D-alanyl)amino-4-deoxy-β-L-arabinopyranoside 

Relevant articles and documents

An expeditious approach to tri-substituted chiral thiazolines

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

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

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)

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

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