1029612-16-5Relevant articles and documents
Stereoselective total syntheses of insect juvenile hormones JH 0 and JH i
Manabe, Atsushi,Ohfune, Yasufumi,Shinada, Tetsuro
experimental part, p. 1213 - 1216 (2012/07/03)
Total syntheses of juvenile hormones JH 0 and JH I have been achieved by a new iterative enol tosylate homologation strategy. Georg Thieme Verlag Stuttgart · New York.
General, robust, and stereocomplementary preparation of β-ketoester enol tosylates as cross-coupling partners utilizing TsCl-N-methylimidazole agents
Nakatsuji, Hidefumi,Ueno, Kanako,Misaki, Tomonori,Tanabe, Yoo
supporting information; body text, p. 2131 - 2134 (2009/05/26)
(Chemical Equation Presented) We have developed a general, robust, and cost-effective method for the (E)- or (Z)-stereocomplementary enol tosylation of β-ketoesters using TsCl-N-methylimidazole (NMI)-Et3N or LiOH. TsCl coupled with NMI formed a