911292-61-0

Upstream product

• 113019-43-5 2,3,4,6-tetra-O-benzyl-1-formyl-D-glucopyranose 
• 343338-28-3 (S)-2-methylpropane-2-sulfinamide 

Downstream Products

• 911292-66-5 2-Methyl-propane-2-sulfinic acid [(R)-((2S,4R)-2-tert-butyl-2,4-dimethyl-5-oxo-[1,3]dioxolan-4-yl)-((2S,3S,4R,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yl)-methyl]-amide 
• 767344-26-3 [(R)-1-((2S,3S,4R,5R,6R)-3,4,5-Tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yl)-ethyl]-carbamic acid 9H-fluoren-9-ylmethyl ester 
• 767344-28-5 (2S,3S,4R,5S,6S)-3,4,5-Tris-benzyloxy-6-[(R)-1-(9H-fluoren-9-ylmethoxycarbonylamino)-ethyl]-tetrahydro-pyran-2-carboxylic acid 
• 911292-78-9 (2S,5R)-5-[(R)-Amino-((2S,3S,4R,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yl)-methyl]-2-tert-butyl-2,5-dimethyl-[1,3]dioxolan-4-one 
• 911292-67-6 2-Methyl-propane-2-sulfinic acid [(S)-((2S,4R)-2-tert-butyl-5-oxo-4-phenyl-[1,3]dioxolan-4-yl)-((2S,3S,4R,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yl)-methyl]-amide 

Relevant academic research and scientific papers

Synthesis of alkylated sugar amino acids: Conformationally restricted l-Xaa-l-Ser/Thr mimics

Two synthetic strategies for the generation of δ-substituted pyranoid sugar amino acids (SAAs) are evaluated. The first employs chiral nonracemic tert-butane sulfinamides as key reagents. Regardless of the stereochemistry of the applied sulfinamide, the p

Stereoselective one-pot synthesis of constrained N,O-orthogonally protected C-glycosyl norstatines [C(1′)-aminoglycosyl-1,3-dioxolan-4-ones]

A procedure for the synthesis of conformationally constrained C-glycosyl norstatines has been developed. The key step of the reaction is the addition of (S)-N-sulfinyl azomethines to chiral (2S)-enolates of dioxolanones which exploits Seebach's "SRS" prin