175848-49-4

Upstream product

• 55378-79-5 C₁₃H₁₅NO₆ 
• 175848-43-8 (3aS,4S,7R,7aS)-7-Amino-4-((S)-1-hydroxy-ethyl)-2,2-dimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-6-one 
• 175848-39-2 Trifluoro-methanesulfonic acid (3aS,4S,7R,7aR)-4-((S)-1-hydroxy-ethyl)-2,2-dimethyl-6-oxo-tetrahydro-[1,3]dioxolo[4,5-c]pyran-7-yl ester 
• 175848-41-6 (3aS,4S,7R,7aS)-7-Azido-4-((S)-1-hydroxy-ethyl)-2,2-dimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-6-one 

Downstream Products

• 175848-48-3 [((1R,2R,6R,7S,11S)-4,4,11-Trimethyl-9-oxo-3,5,8,10-tetraoxa-tricyclo[5.2.2.0^2,6]undec-1-ylcarbamoyl)-methyl]-carbamic acid benzyl ester 

Relevant academic research and scientific papers

Mimics of L-rhamnose: Analogues of rhamnopyranose containing a constituent α-amino acid at the anomeric position. A rhamnopyranose analogue of hydantocidin

Ionic brominative oxidation of 2-amino derivatives of protected heptonolactones derived from L-rhamnose provides a key bicyclic intermediate for the synthesis of analogues of L-rhamnopyranose with spirohydantoins and spirodiketopiperazines at the anomeric