1444800-32-1

Upstream product

• 1444800-43-4 (3aS,4S,6aR)‐4‐(((1S,2R,5S)‐2‐isopropyl‐5‐methylcyclohexyl)oxy)‐3,3a,4,6a‐tetrahydro‐6H‐furo[3,4‐c]pyrazol‐6‐one 
• 122079-41-8 (5S)-(D-menthyloxy)-2(5H)-furanone 
• 15356-60-2 (1S,2R,5S)-(+)-menthol 

Downstream Products

• 1444800-55-8 methyl (1R,2S)‐2‐(((benzyloxy)imino)methyl)cyclopropane‐1‐carboxylate 
• 1444800-61-6 methyl (1R,2S)‐2‐(((benzyloxy)amino)methyl)cyclopropane‐1‐carboxylate 
• 1444800-67-2 (1R,2S)‐2‐(((benzyloxy)(tert‐butoxycarbonyl)amino)methyl)cyclopropane‐1‐carboxylate 

Relevant academic research and scientific papers

Four Stereoisomers of 2-Aminomethyl-1-cyclopropanecarboxylic Acid: Synthesis and biological evaluation

Here, we report a practical method for asymmetric synthesis of cyclopropane-fused GABA analogs. Starting from 2-furaldehyde, the cis-isomer (CAMP) was synthesized over 10 steps; (1)- and (+)-CAMP￠HCl were synthesized by employing d- and l-menth

A synthesis of (-)- cis -2-aminomethylcyclopropanecarboxylic acid [(-)-CAMP]

An enantioselective synthesis of (-)-cis-2- aminomethylcyclopropanecarboxylic acid [(-)-CAMP] has been achieved in 2.5% total yield over ten steps starting from 2-furaldehyde. The synthesis features diastereoselective cyclopropane formation via diazene, followed by oxime formation and the reduction, for construction of the γ-aminobutyric acid (GABA) motif. Georg Thieme Verlag Stuttgart · New York.