327611-80-3

Upstream product

• 103-72-0 phenyl isothiocyanate 
• 327611-76-7 (1R,2R,3S,5R)-2-amino-3-hydroxymethyl-2,6,6-trimethylbicyclo[3.1.1]heptane 
• 7785-26-4 (-)-α-pinene 
• 705949-02-6 C₁₂H₂₁NO₂ 
• 327611-75-6 ethyl (1R,2R,3S,5R)-2-amino-2,6,6-trimethylbicyclo[3.1.1]heptane-3-carboxylate 
• 328010-06-6 (1R,2R,5S,7R)-2,8,8-trimethyl-3-azatricyclo[5.1.1.0^2,5]nonan-4-one 

Relevant academic research and scientific papers

Stereoselective synthesis and Cytoselective toxicity of Monoterpene-fused 2-Imino-1,3-Thiazines

Starting from pinane-, apopinane- and carane-based 1,3-amino alcohols obtained from monoterpene-based ?-amino acids, a library of monoterpene-fused 2-imino-1,3-Thiazines as main products and 2-Thioxo-1,3-oxazines as side-products were prepared via two- or

Synthesis and transformations of enantiomeric 1,2-disubstituted monoterpene derivatives

Regio- and stereospecific addition of chlorosulfonyl isocyanate to (+)- and (-)-α-pinene 1 resulted in enantiomerically pure β-lactams 2, which were converted to enantiomeric β-amino esters 3 and 1,3-amino alcohols 4 and 6 with ee >99%. The resulting 1,3-