127801-86-9Relevant articles and documents
Synthesis and fungistatic activity of bicyclic lactones and lactams against Botrytis cinerea, Penicillium citrinum, and Aspergillus glaucus
Walczak, Paulina,Pannek, Jakub,Boratyński, Filip,Janik-Polanowicz, Agata,Olejniczak, Teresa
, p. 8571 - 8578 (2014)
Six analogues of natural trans-4-butyl-cis-3-oxabicyclo[4.3.0]nonan-2-one (3) and three derivatives, 11, 12, and 13, of Vince lactam (10) were synthesized and tested as fungistatic agents against Botrytis cinerea AM235, Penicillium citrinum AM354, and six
2-azabicyclo[2.2.1]hept-5-en-3-one epoxide: A versatile intermediate for the synthesis of cyclopentyl carbocyclic 2-deoxy-, 3-deoxy- and ara- ribonucleoside analogues.
Dominguez, Belen M.,Cullis, Paul M.
, p. 5783 - 5786 (2007/10/03)
5,6-Epoxy-exo-2-azabicyclo[2.2.1]heptan-3-one has been used as a versatile intermediate in the synthesis of 2-deoxy-, 3-deoxy- and ara- cyclopentyl carbocyclic nucleosides. An efficient, short synthesis of the (+) carbocyclic thymidine 13 is reported.
Epoxidation of 2-Azabicyclohept-5-en-3-one
Legraverend, Michel,Bisagni, Emile,Huel, Christiane
, p. 1881 (2007/10/02)
Epoxidation of 2-azabicyclohept-5-en-3-one has been performed in high yield with potassium hydrogen persulfate at pH 6, 1H nmr data indicate an exo stereoconfiguration of the epoxide.