14783-85-8

Upstream product

• 121-46-0 bicyclo[2.2.1]hepta-2,5-diene 
• 698-16-8 benzohydroximoyl chloride 
• 622-42-4 1-nitro-1-phenylmethane 

Downstream Products

• 1006-65-1 3-phenylisoxazole 
• 132576-79-5 5,8-methano-r-4-phenyl-2-phenylimino-c-4a,c-5,c-8,c-8a-tetrahydro-4H-1,3-benzoxazine 
• 132576-77-3 5,8-methano-r-4-phenyl-2-p-tolyl-c-4a,c-5,c-8,c-8a-tetrahydro-4H-1,3-benzoxazine 
• 132576-83-1 5,8-methano-r-4-phenyl-c-4a,c-5,c-8,c-8a-tetrahydro-4H-1,3-benzoxazin-2(3H)-thione 
• 132576-81-9 5,8-methano-r-4-phenyl-c-4a,c-5,c-8,c-8a-tetrahydro-4H-1,3-benzoxazin-2(3H)-one 
• 132532-95-7 4-phenyl-2-oxa-3-aza-r-1,c-5,c-6,c-7,t-8,t-11,c-12,c-13-pentacyclo<8.3.1^8,11.1^6,13.0^7,12>pentadeca-3,9-diene 
• 132745-99-4 exo-3-aminophenylmethyl-bicyclo<2.2.1>hex-5-en-exo-2-ol 

Relevant academic research and scientific papers

Molybdenum-mediated cleavage reactions of isoxazoline rings fused in bicyclic frameworks

(matrixpresented) The molybdenum-mediated cleavage reactions of isoxazoline rings fused in bicyclic frameworks were investigated. A tandem N-O bond cleavage-retro aldol reaction of an isoxazoline ring fused in a bicyclic framework led to the cleavage of t

Preparation and Stereostructure of Norbornane/ene-Condensed Phenyl-Substituted O,N-Heterocycles

Norbornane/ene di-exo-condensed isoxazolines were reduced to amino alcohols and then cyclized to 1,3-oxazines.The phenylimino analogues, 1,3-oxazin-2(3H)-ones, the corresponding 2(3H)-thiones and 1,4-oxazepin-3(4H)-ones were also prepared.The structures,