107553-97-9Relevant academic research and scientific papers
Synthesis of Macrocyclic Terpenoids by Intramolecular Cyclization. 12. Total Synthesis of Methyl Ceriferate I, a 14-Membered Ring Sesterterpene from Scale Insects
Kodama, Mitsuaki,Shiobara, Yoshinori,Sumitomo, Hisako,Fukuzumi, Kazuyoshi,Minami, Hiroyuki,Miyamoto, Yasuko
, p. 1437 - 1441 (2007/10/02)
Total synthesis of (+/-)-methyl ceriferate I (6), the methyl ester of a cembrane-type sesterterpene isolated from the wax of scale insects, was achieved by means of Wadsworth-Emmons olefination as key step.Three segments, 9, 10, and 11, were connected to
SYNTHESIS OF MACROCYCLIC TERPENOIDS BY INTRAMOLECULAR CYCLIZATION X. TOTAL SYNTHESIS OF METHYL CERIFERATE-I
Kodama, Mitsuaki,Shiobara, Yoshinori,Sumitomo, Hisako,Fukuzumi, Kazuyoshi,Minami, Hiroyuki,Miyamoto, Yasuko
, p. 2157 - 2160 (2007/10/02)
The methyl ester of (+/-)-ceriferic acid-I, a 14-membered ring sesterterpene isolated from the wax of the scale insect Ceroplastes ceriferus, was synthesized by means of an intramolecular Wittig-type reaction.
