120293-49-4

Upstream product

• 111-30-8 Glutaraldehyde 

Downstream Products

• 49620-06-6 (+)-isonitramine 
• 120186-06-3 C₃₂H₃₃NO₄ 
• 120186-09-6 Methanesulfonic acid (7S,11R)-2-benzyl-11-(tert-butyl-dimethyl-silanyloxy)-2-aza-spiro[5.5]undec-7-yl ester 
• 120186-03-0 Methanesulfonic acid (7R,11S)-11-hydroxy-2-((R)-2-hydroxy-1-phenyl-ethyl)-2-aza-spiro[5.5]undec-7-yl ester 
• 120186-07-4 (7S,11R)-11-(tert-Butyl-dimethyl-silanyloxy)-2-((R)-2-hydroxy-1-phenyl-ethyl)-2-aza-spiro[5.5]undecan-7-ol 
• 120210-97-1 (R)-2-Benzyl-11-(tert-butyl-dimethyl-silanyloxy)-2-aza-spiro[5.5]undec-7-ene 
• 120186-08-5 (7S,11R)-2-Benzyl-11-(tert-butyl-dimethyl-silanyloxy)-2-aza-spiro[5.5]undecan-7-ol 
• 120186-04-1 5-[1-((R)-2-Hydroxy-1-phenyl-ethyl)-piperidin-(3E)-ylidene]-pentan-1-ol 
• 120186-01-8 C₁₉H₂₅NO₅S 

Relevant academic research and scientific papers

ASYMMETRIC SYNTHESIS XV: ENANTIOSPECIFIC SYNTHESIS OF (+) AND (-) ISONITRAMINES FROM A COMMON CHIRAL INTERMEDIATE.

The enantiospecific synthesis of (+) and (-) isonitramines 7 has been achieved from a common chiral intermediate 5; this key compound was formed by condensation of two molar equivalents of glutaraldehyde with one mole of (-) phenylglycinol.