93474-89-6

Upstream product

• 84246-93-5 methyl N-benzyl-N-(3-cyclohexenyl)carbamate 
• 124-38-9 carbon dioxide 
• 141330-12-3 N-benzyl-N-(2-cyclohexenyl)amine 
• 6181-92-6 dichlorure de l'acide N-(phenylmethyl) carbonimidique 
• 100-46-9 benzylamine 
• 93474-88-5 O-3-cyclohexenyl O'-methyl N-benzylcarbonimidate 
• 6392-79-6 methyl N-benzylchloroformimidate 

Downstream Products

• 93474-96-5 3-benzyl-3aα,4,5,7aα-tetrahydrobenzoxazolin-2-one 
• 93474-90-9 3-benzyl-7-hydroxy-3aα,4,5,6,7β,7aα-hexahydrobenzoxazolin-2-one 
• 93474-90-9 (3aR,7S,7aR)-3-Benzyl-7-hydroxy-hexahydro-benzooxazol-2-one 

Relevant academic research and scientific papers

A One-Pot Iodo-Cyclization/Transition Metal-Catalyzed Cross-Coupling Sequence: Synthesis of Substituted Oxazolidin-2-ones from N-Boc-allylamines

A one-pot iodo-cyclization/transition metal-catalyzed cross-coupling sequence is reported to access various C5-functionalized oxazolidin-2-ones from unsaturated N-Boc-allylamines. Depending on the Grignard reagents used for the cross-coupling, e.g., aryl- or cyclopropylmagnesium bromide, a cobalt or copper catalyst has to be used to obtain the functionalized oxazolidin-2-ones in good yields.

Convenient synthesis of oxazolidinones and oxazinones from allyl and homoallyl amines under mild conditions

An efficient one-pot general method for the high-yield synthesis in solution of oxazolidinones and oxazinones from allyl- and homoallylamines, respectively, has been developed. The reaction is carried out at an atmospheric pressure between 0°C and room te

Synthesis of Protected Aminocyclohexanediols

As the model study for the synthesis of aminocyclitols and amino sugars, 2-cyclohexen-1-ol (1) was converted to five of the seven possible (1,2,3)-aminocyclohexanediols in protected form (4a, 6a, 11a, 13a, and 18a).Two flexible new approaches were employe