61145-11-7

Upstream product

• 21572-32-7 2-chloro-1-phenyl-ethanone oxime 
• 53441-57-9 1-chloro-1-nitroso-1-phenylethane 
• 613-91-2 acetophenone oxime 

Downstream Products

• 61145-14-0 4a,7a-dihydro-3-phenyl-4H-furo[2,3-e]-1,2-oxazine 
• 61145-16-2 3-phenyl-4,4a,5,7a-tetrahydro-cyclopenta[e][1,2]oxazine 
• 61145-15-1 4a,7a-dihydro-4a,6-dimethyl-3-phenyl-4H-furo<2,3-e>-1,2-oxazine 
• 83670-30-8 2,9a-Diphenyl-3,5a,8,8a,9,9a-hexahydro-cyclopenta[e]imidazo[1,2-b][1,2]oxazine 1-oxide 
• 133350-21-7 5,6-Dihydro-6-methoxy-6-methyl-5-methylene-3-phenyl-4H-1,2-oxazine 
• 117341-58-9 5,6-Dihydro-6-methoxy-5-methylene-3-phenyl-4H-1,2-oxazine 
• 117341-64-7 5,6-Dihydro-6-(1-hydroxyethyl)-6-methoxy-5-methylene-3-phenyl-4H-1,2-oxazine 
• 117369-63-8 5,6-Dihydro-6-(1-hydroxy-1-methylethyl)-6-methoxy-5-methylene-3-phenyl-4H-1,2-oxazine 
• 100181-21-3 3,6-diphenyl-6-trimethylsilyl-4H-1,5,2-oxathiazine 
• 100181-20-2 3,6-diphenyl-6-triphenylsilyl-4H-1,5,2-oxathiazine 

Relevant academic research and scientific papers

The [4+2]-Cycloaddition of α-Nitrosoalkenes with Thiochalcones as a Prototype of Periselective Hetero-Diels–Alder Reactions—Experimental and Computational Studies

The [4+2]-cycloadditions of α-nitrosoalkenes with thiochalcones occur with high selectivity at the thioketone moiety of the dienophile providing styryl-substituted 4H-1,5,2-oxathiazines in moderate to good yields. Of the eight conceivable hetero-Diels–Ald

A new method for the generation of α-nitrosoolefins from ketooximes and its application to the synthesis of 5,6-dihydro-4H-1,2-oxazine derivatives [1]

Reaction of ketooximes containing α-methylene group with chloramine-T followed by treatment with triethylamine leads to the formation of α-nitrosoolefins via α-nitrosochloride, which can react in situ intermolecularly with olefinic compounds to produce 5,

Theoretical Prediction and Experimental Tests of Conformational Switches in Transition States of Diels-Alder and 1,3-Dipolar Cycloadditions to Enol Ethers

Transition structures for the cycloadditions of butadiene, acrolein, nitrosoethylene, and methyl-enenitrone to 1-butene, silyl vinyl ether, and methyl vinyl ether have been located using ab initio RHF theory with the 3-21G basis set and with density funct

A New Mode of Addition of α-Nitrosostyrenes

Treatment of the two known (oxazine) 1,4-adducts of α-nitrosostyrene and either 2,5-dimethylfuran or cyclopentadiene with further nitrosostyrene gives nitrones, products of 1,3-addition at the oximino C=N.