3613-30-7Relevant articles and documents
Quistad et al.
, p. 299,300 (1975)
Universal approach to the synthesis of juvenoid hydroprene and methoprene from 4-methyltetrahydropyran
Ishmuratov,Yakovleva,Galyautdinova,Faifer,Kharisov,Zorin,Tolstikov
, p. 486 - 489 (2007/10/03)
A universal approach to the synthesis of juvenoid hydroprene and methoprene was developed on the basis of monoalkylation of acetoacetate by 1-acetoxy-5-bromo-3-methylpentane, the product of acidic decyclization of 4-methyltetrahydropyran.
PREPARATION OF DERIVATIVES OF CITRONELLAL
Koertvelyessy, Gyula
, p. 347 - 354 (2007/10/02)
The hydrogenation of citronellal and citral, if not separated from ethereal oils, leads regioselectively to dihydrocitronellal and citronellal, respectively.The reaction of citral with (+)-ephedrin or L-aspartic acid, followed by hydrogenation and deblocking the aldehyde function, yields optically active citronellal.Reacting the aldehyde function of citronellal with diethanolamine, piperidine or morpholine, the alcohol addition to the 6,7-double bond results in 7-alkoxy substituted citronellals with acceptable yield.The formation of 7-hydroxy-6,7-dihydrocitronellal during this reaction has been proved and the effect of reaction parameters on the yield have been discussed.
Cob(I)alamine as catalyst. I. Communication. Reduction of saturated nitriles in aqueous solution
Fischli
, p. 2560 - 2578 (2007/10/08)
-