129441-80-1

Upstream product

• 59438-62-9 3-benzoyl-2-oxa-3-azabicyclo<2.2.1>hept-5-ene 
• 59438-62-9 3-oxa-2-aza-bicyclo[2.2.1]hept-5-en-2-yl(phenyl)methanone 

Downstream Products

• 657397-07-4 N-(5-iso-butylidene-4-oxocyclopent-2-enyl)-benzamide 
• 129441-82-3 N-[(1S,2S,3S)-2-(Methoxy-phenylsulfanyl-methyl)-3-methyl-4-oxo-cyclopentyl]-benzamide 
• 129743-74-4 (2S,3R,4S)-4-Benzoylamino-2-methyl-6-oxo-tetrahydro-pyran-3-carboxylic acid methyl ester 
• 129743-73-3 (1R,2R,5R)-5-Benzoylamino-2-methyl-3-oxo-cyclopentanecarboxylic acid methyl ester 
• 129441-81-2 N-[(1R,2R,3R)-2-(Methoxy-phenylsulfanyl-trimethylsilanyl-methyl)-3-methyl-4-oxo-cyclopentyl]-benzamide 

Relevant academic research and scientific papers

Intra- and intermolecular hydrogen bonding effects in cycloadditions between nitrile oxides and 4-benzoylamino-2-cyclopenten-1-ol and its derivatives

Cycloadditions between nitrile oxides and cis-4-benzoylamino-2-cyclopenten-1-ol offer an example in which a strong intramolecular hydrogen bond completely offsets the syn-directing ability of the cyclopentene substituents. Solvents affected the conformational equilibrium of the cyclopentene dipolarophile but did not sizeably influence the cycloaddition selectivity, showing the absence of directing effects between the addends. Removal of the intramolecular hydrogen bond by OH protection or oxidation activated the syn-directing ability of the amido substituent and provided a convenient route to syn stereoselection. Wiley-VCH Verlag GmbH, 69451 Weinheim, Germany, 2002.

Stereoselective cycloadditions of acyl-nitroso compounds; an approach to carbapenem synthesis

The adduct obtained from cyclopentadiene and benzohydroxamic acid under oxidising conditions has been used in a stereoselective synthesis of the N-benzoyl derivative of a known intermediate for carbapenen synthesis.