561285-40-3

Upstream product

• 150686-70-7 (R)-4-((tert-butyldimethylsilyl)oxy)-2-iodocyclopent-2-en-1-one 
• 561285-38-9 (+)-4-benzyloxy-8-[(4-methylphenyl)sulfonyl]-6-oxa-8-azabicyclo[3.2.1]-oct-2-yl acetate 
• 561285-35-6 (-)-4-benzyloxy-8-[(4-methylphenyl)sulfonyl]-6-oxa-8-azabicyclo[3.2.1]-octan-2-one 
• 561285-41-4 (+)-8-[(4-methylphenyl)sulfonyl]-6-oxa-8-azabicyclo[3.2.1]oct-3-en-2-one 
• 64757-64-8 L-furylglycine 
• 561285-39-0 (+)-5-benzyloxy-2-(hydroxymethyl)piperidin-3-ol 
• 155404-19-6 (3R,5S)-3,5-Bis-(tert-butyl-dimethyl-silanyloxy)-1-(tert-butyl-dimethyl-silanyloxymethyl)-cyclopentene 
• 1026377-49-0 (1S,4R)-1,4-di-(tert-butyldimethylsilyloxy)-2-iodocyclopent-2-ene 
• 159835-73-1 (1S,4R)-4-(tert-Butyl-dimethyl-silanyloxy)-2-iodo-cyclopent-2-enol 
• 61305-35-9 (R)-4-((tert-butyldimethylsilyl)oxy)cyclopent-2-enone 

Relevant academic research and scientific papers

Chemoenzymatic synthesis of 1,3-dideoxynojirimycin

Enone 3, readily available from cyclopentadiene, was transformed via Pd(0)-mediated carbon monoxide coupling, ozonolysis and reductive amination to enantiopure 1,3-dideoxynojirimycin (7) in high diastereoselectivity.

An aza analogue of iso-levoglucosenone: Synthesis and application of a new building block for imino sugars

The aza analogue 3 of iso-levoglucosenone, which is easily accessible from furylglycine, was used as a flexible building block for the synthesis of various imino sugars. Enantiomerically pure products are available starting from optically active furylglycine derivatives. ( Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003).