115014-76-1

Upstream product

• 1436-60-8 ethyl trans-2-amino-1-cyclohexanecarboxylate 
• 555-16-8 4-nitrobenzaldehdye 
• 1436-60-8 ethyl cis-2-amino-1-cyclohexanecarboxylate 

Downstream Products

• 114950-65-1 (r-4a,t-2,t-8a)-3-methyl-2-p-nitrophenylperhydroquinazolin-4-one 
• 114950-65-1 (r-4a,c-2,c-8a)-3-methyl-2-p-nitrobenzylideneperhydroquinazoline-4-one 
• 114950-65-1 (r-4a,t-2,c-8a)-3-methyl-2-p-nitrobenzylideneperhydroquinazoline-4-one 
• 114950-64-0 (r-4a,t-2,c-8a)-2-p-nitrophenylperhydroquinazolin-4-one 
• 114950-66-2 (1R,2S)-2-{[1-(4-Nitro-phenyl)-meth-(E)-ylidene]-amino}-cyclohexanecarboxylic acid amide 
• 114950-64-0 (r-4a,c-2,c-8a)-2-p-nitrophenylperhydroquinazolin-4-one 
• 114950-64-0 (r-4a,t-2,t-8a)-2-p-nitrophenylperhydroquinazolin-4-one 
• 114950-66-2 (1S,2S)-2-{[1-(4-Nitro-phenyl)-meth-(E)-ylidene]-amino}-cyclohexanecarboxylic acid amide 

Relevant academic research and scientific papers

STEREOCHEMICAL STUDIES, 133; SATURATED HETEROCYCLES, 137 SYNTHESIS AND STERIC STRUCTURE OF STEREOISOMERIC 2-p-NITROPHENYLPHENYLHYDROQUINAZOLIN-4-ONES

Ethyl cis- and trans-2-aminocyclohexanecarboxylate (4) were used as starting material to prepare (r-4a,t-2,t-8a)-, (r-4a,c-2,c-8a)- and (r-4a,t-2,c-8a)-2-p-nitrophenylperhydroquinazolin-4-one and their 3-methyl-substituted derivatives in stereospecific or