124738-95-0

Upstream product

• 593-56-6 N-methoxylamine hydrochloride 
• 18039-26-4 2,3,4-tri-O-benzyl-D-xylopyranose 

Downstream Products

• 124738-96-1 2,3,4-tris-O-(phenylmethyl)-D-xylo-pentos-5-ulose 1-(O-methyloxime) 
• 1227292-02-5 C₂₈H₃₃NO₇S 
• 124738-98-3 (1S,6S,7R,8S,9S)-7,8,9-tribenzyloxy-2-methoxy-2-azabicyclo<4.3.0>non-4-ene 
• 124738-97-2 (2R,3S,4R)-tribenzyloxy-octa-5(E,Z),7-diene-1-al syn and anti O-methyloximes 
• 300547-66-4 [1R-(1α,2α,3β,4α,5β)]-2-(methoxyamino)-3,4,5-tris(phenylmethoxy)cyclopentanol 
• 300547-64-2 [1S-(1α,2β,3α,4β,5α)]-2-(methoxyamino)-3,4,5-tris(phenylmethoxy)cyclopentanol 
• 300547-69-7 [1R-(1α,2α,3β,4α,5β)]-2-amino-3,4,5-tris(phenylmethoxy)cyclopentanol 

Relevant academic research and scientific papers

THIOPYRANOSE COMPOUND AND METHOD FOR PRODUCING SAME

There is provided a production method of a thiopyranose compound represented by the following Formula (2) by reacting a compound represented by the following Formula (1) with a sulfur compound. X represents a leaving group. A represents an oxygen atom or

A practical synthesis of sugar-derived cyclic nitrones: Powerful synthons for the synthesis of iminosugars

Sugar-derived cyclic nitrones were synthesized from the corresponding aldoses through an efficient and practical procedure involving a seven-step reaction sequence in good to excellent overall yield (10-42%). This synthetic strategy, requiring only inexpe

Radical cyclization in heterocycle synthesis. Part 9: A novel synthesis of aminocyclitols and related compounds via stannyl radical cyclization of oxime ethers derived from sugars

Stannyl radical addition-cyclization of oxime ethers derived from D-glucose, D-galactose, and D-xylose proceeded smoothly to afford alkoxyamino alcohols which were effectively converted into two types of glycosidase inhibitors or its candidates such as aminocyclitols, 1-deoxynojirimycin, and 1-deoxygalactostatin via reductive ring-expansion of trans alkoxyamino alcohols. (C) 2000 Elsevier Science Ltd.

INTRAMOLECULAR REACTIONS OF COMPOUNDS DERIVED FROM SUGARS. PART II. STEREOCONTROLLED INTRAMOLECULAR DIELS-ALDER CYCLIZATIONS OF 1,6(E,Z),8-NONATRIENES AND 1-AZA-6(E,Z),8-NONANTRIENES

Intramolecular Diels-Alder reactions of E,Z mixtures of nonatrienes 6 and 9 led to the exclusive formation of the bicyclic compounds 10 and 11 respectively.