Search results for "Heptane"
showing 3 items of 103 documents
Stereoselective synthesis of 7,11-guaien-8,12-olides from santonin. Synthesis of podoandin and (+)-zedolactone A.
2000
Photochemical rearrangement of hydroxy ester 2, easily obtained from santonin (1), afforded butenolide 4, a good starting material for the synthesis of 7,11-guaien-8,12-olides. Compound 4 has been transformed into compound 10, which has been used for the synthesis of podoandin (5) and (+)-zedolactone A (ent-6). Regioselective elimination of the acetyl group on C10 afforded directly podoandin (5). For the synthesis of ent-6, a hydroxyl group has been regio- and stereoselectively introduced at the 4alpha-position through the 3alpha,4alpha-epoxide 15. The basic hydrolysis of the 10-acetyl group in compound 18 took place with concomitant intramolecular conjugated addition of the alkoxide to the…
Polymer ester von sären des phosphors, 7. Polymerisation des 1-oxo-2,6,7-trioxa-1-phosphabicyclo[2.2.1]heptans
1981
1-Oxo-2,6,7-trioxa-1-phosphabicyclo[2.2.1]heptane is transformed in situ (prepared from trimethyl phosphite and glycerol) at −78°C in the presence of a trace of water into a crosslinked polymer containing constitutional repeating units with 5- and 6-membered rings. The reaction with reagents containing hydroxyl groups (water, acetic acid, alcohol) leads to the degradation of the network with the formation of soluble fragments with Pn = 35–50. This reactivity and the possibility to obtain other derivatives from the fragments make this polymer a carrier for pharmacologically active polymers with the advantage of decomposing only into the innocuous components phosphoric acid and glycerol.
CCDC 245603: Experimental Crystal Structure Determination
2004
Related Article: R.Herchel, R.Boca, M.Gembicky, J.Kozisek, F.Renz|2004|Inorg.Chem.|43|4103|doi:10.1021/ic035374i