72551-11-2

Upstream product

• 1197-51-9 N-propargylbenzylamine 
• 201230-82-2 carbon monoxide 
• 72551-10-1 N-(2-bromoallyl)benzylamine 
• 328241-59-4 N-benzyl-N-prop-2-ynyl-(1-methyl)cyclohexa-2,5-diene-1-carboxamide 
• 100-46-9 benzylamine 
• 220116-40-5 1-Benzyl-3-methyl-3-phenylselanyl-azetidin-2-one 
• 87672-77-3 N-benzyl-β,β'-dibromoisobutyramide 

Downstream Products

• 96850-92-9 N-benzyl-3-methylene-4-methoxy-β-lactam 
• 96850-98-5 N-methoxybenzyl-3-methylene-β-lactam 
• 72551-14-5 N-benzyl-2-((benzylamino)methyl)acrylamide 
• 34317-15-2 1-benzyl-3-methylazetidin-2-one 
• 87672-80-8 1-Benzyl-3-methylene-azetidine-2-thione 
• 75986-05-9 1-benzyl-3-hydroxy-3-hydroxymethyl azetidin-2-one 
• 75986-07-1 N-benzylazetidine-2,3-dione 
• 75986-09-3 1-benzyl azetidine-2,3-dion-3-oxime 
• 75986-11-7 3-acetylamino-1-benzyl azetidin-2-one 
• 1129612-44-7 1-benzyl-3-(pentan-2-ylidene)-azetidin-2-one 
• 1129612-42-5 1-benzyl-3-(pentan-2-ylidene)-azetidin-2-one 
• 1129611-86-4 1-benzyl-3-butylideneazetidin-2-one 
• 1129611-52-4 1-benzyl-3-butylideneazetidin-2-one 
• 1129611-94-4 3-(1-benzyl-2-oxoazetidin-3-ylidene)propyl acetate 

Relevant academic research and scientific papers

Preparation of β- and γ-lactams via ring closures of unsaturated carbamoyl radicals derived from 1-carbamoyl-1-methylcyclohexa-2,5-dienes

l-Carbamoyl-1-methylcyclohexa-2,5-dienes produced the corresponding delocalised 1-carbamoyl-1-methylcyclohexa-2,5-dienyl radicals on treatment with radical initiators. At temperatures above ca. 300 K dissociation to produce toluene and aminoacyl (carbamoy

Direct amino-phenylselenylation of enoates: An easy route to α- phenylseleno-β-amino esters and β-lactams

A 'one-pot' procedure to obtain α-phenyiseleno-β-amino esters from the corresponding enoates is described. The target compounds are useful synthetic tools and direct precursors of new α-phenylseleno-β-lactams, which can be easily transformed into their α-

Synthesis of α,β-unsaturated lactams by palladium-catalysed intramolecular carbonylative coupling

Amino vinyl triflates have been shown to undergo an intramolecular, carbonylative coupling in the presence of a palladium catalyst to afford α,β-unsaturated lactams.

Organic Iodide Aided Carbonylation of Terminal Acetylenes with Palladium Catalyst

Carbonylation of various terminal acetylenes in the presence of a catalytic amount of organic iodides or amine * HI salt and palladium complexes was found to produce 2-substituted acrylamides in good yields under mild conditions (5 atm, 120 deg C, 6h).

SYNTHESE DE METHYLENE-3 AZETIDINONES-2 PAR TRANSFERT DE PHASE SOLIDE/LIQUIDE ET PREPARATION DE LEURS ANALOGUES THIOXO

The reaction of 3-bromo-2-bromomethylpropionamides with pulverized potassium hydroxyde gave 3-methylene-2-azetidinones in fair to good yields.These compounds were converted by thiation to the so far unknown 3-methylene-2-azetidinethiones.

A Novel Synthesis of (+/-)-3-Aminonocardinic Acid

(+/-)-3-Aminonocardinic acid, which is an important starting material for the synthesis of nocardicin A and other biologically active analogues, has been synthesized by application of a new method for synthesis of α-methylene-β-lactams.