700380-06-9

Downstream Products

• 816453-04-0 (1R,3aS,5S,7aS)-4-Dibenzylamino-5-((S)-1-hydroxy-propyl)-1-oxo-2-((R)-1-phenyl-ethyl)-1,2,3a,4,5,7a-hexahydro-1λ⁴-isothiazolo[4,5-b]pyridin-3-one 
• 816452-97-8 (1R,3aS,5S,7aS)-4-Dimethylamino-5-((S)-hydroxy-phenyl-methyl)-1-oxo-2-((R)-1-phenyl-ethyl)-1,2,3a,4,5,7a-hexahydro-1λ⁴-isothiazolo[4,5-b]pyridin-3-one 
• 1025823-13-5 (2S,3S,6S)-1-Dimethylamino-6-((S)-hydroxy-phenyl-methyl)-2-((R)-1-phenyl-ethylcarbamoyl)-1,2,3,6-tetrahydro-pyridine-3-sulfinic acid 
• 816453-10-8 (2R,6S)-1-Dibenzylamino-6-((S)-1-hydroxy-propyl)-1,2,5,6-tetrahydro-pyridine-2-carboxylic acid ((R)-1-phenyl-ethyl)-amide 
• 1027279-83-9 (2S,3S,6S)-1-Dibenzylamino-6-((S)-1-hydroxy-propyl)-2-((R)-1-phenyl-ethylcarbamoyl)-1,2,3,6-tetrahydro-pyridine-3-sulfinic acid 
• 816452-90-1 (2R,6S)-1-(Benzyl-trimethylsilanylmethyl-amino)-6-((S)-1-hydroxy-propyl)-1,2,5,6-tetrahydro-pyridine-2-carboxylic acid ((R)-1-phenyl-ethyl)-amide 
• 1028286-46-5 (2S,3S,6S)-1-Dimethylamino-6-((S)-1-hydroxy-propyl)-2-((R)-1-phenyl-ethylcarbamoyl)-1,2,3,6-tetrahydro-pyridine-3-sulfinic acid 
• 1026913-82-5 C₁₈H₂₁N₃O₄ 
• 816453-11-9 (1S,5R,8aS)-1-Ethyl-3-oxo-1,5,8,8a-tetrahydro-oxazolo[3,4-a]pyridine-5-carboxylic acid ((R)-1-phenyl-ethyl)-amide 
• 700380-12-7 (2R,6S)-6-((S)-1-Hydroxy-propyl)-1,2,5,6-tetrahydro-pyridine-2-carboxylic acid ((R)-1-phenyl-ethyl)-amide 
• 816452-89-8 (1R,3aS,5S,7aS)-4-(Benzyl-trimethylsilanylmethyl-amino)-5-((S)-1-hydroxy-propyl)-1-oxo-2-((R)-1-phenyl-ethyl)-1,2,3a,4,5,7a-hexahydro-1λ⁴-isothiazolo[4,5-b]pyridin-3-one 
• 816453-02-8 (1R,3aS,5S,7aS)-4-Dimethylamino-5-((S)-1-hydroxy-propyl)-1-oxo-2-((R)-1-phenyl-ethyl)-1,2,3a,4,5,7a-hexahydro-1λ⁴-isothiazolo[4,5-b]pyridin-3-one 

Relevant academic research and scientific papers

Design of a nonreductive method for chemoselective cleavage of hydrazines in the presence of unsaturations: Application to a stereoconvergent three-component synthesis of (-)-methyl palustramate

A chemoselective hydrazine (N-N) cleavage methodology that preserves the integrity of alkenes was developed based on a mild acid-promoted fragmentation of tetrasubstituted 1-(trimethylsilylmethyl)-1-benzylhydrazines. This strategy was applied to a concise