95531-99-0Relevant academic research and scientific papers
Synthesis of the C17-C25 subunit of lasonolide A utilizing a Tsuchihashi-Yamamoto type rearrangement
Sawant, Kailas B.,Ding, Fei,Jennings, Michael P.
, p. 5177 - 5180 (2008/02/08)
An efficient synthesis of the C17-C25 subunit resident in (-)-lasonolide A is reported herein. The key reaction features that were utilized include a Tsuchihashi-Yamamoto type rearrangement and Molander-Reformatsky SmI2 me
Synthesis of (+)-prelactone B
Chakraborty, Tushar K.,Tapadar, Subhasish
, p. 2541 - 2543 (2007/10/03)
Radical-mediated opening of a trisubstituted epoxy alcohol using cp2TiCl was followed by diastereoselective reduction of the resulting product with a centrally located methylene group, flanked on both sides by two chiral hydroxyl-bearing carbon
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.
