The azomethine ylide is generated in situ, meaning that it's formed and used immediately in the reaction without isolation. This is done to prevent the decomposition of the reactive intermediate.
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3,4-Pyrrolidinedicarboxylic acid, dimethyl ester, (3R,4R)-rel-
FORMALDEHYDE
Toluene
C54H58Si2
ethyl 2-((ethoxycarbonyl)amino)benzoate
1-Ethyl-2-(ethylthio)benzene
[(2-tert-butyl-6-(4-fluorophenyl)pyridine(-2H))Pt(PPh3)]
C48H46N4O10S2
3-(3,5-dimethoxybenzoyl)benzoic acid
Benzamide, N-[(benzoylamino)diphenylphosphoranylidene]-
C13H12NP
(E)-1-phenylpropan-1-one O-acetyl oxime
Trimethyl-((E)-5-methyl-3-phenyl-hexa-2,5-dienyloxy)-silane
Ethanol, 2-[(1-methylethyl)(phenylmethyl)amino]-
2,3-bis(phenylthio)furo[3,2-b]pyridine
