377751-09-2Relevant articles and documents
Total synthesis of macquarimicins using an intramolecular Diels-Alder approach inspired by a biosynthetic pathway
Munakata, Ryosuke,Katakai, Hironori,Ueki, Tatsuo,Kurosaka, Jun,Takao, Ken-Ichi,Tadano, Kin-Ichi
, p. 11254 - 11267 (2007/10/03)
A total synthesis of the macquarimicins A-C (1-3), novel natural products with intriguing tetra- or pentacyclic frameworks, has been achieved. The synthesis features an extensive investigation of the biosynthesis-based intramolecular Diels-Alder (IMDA) re
Synthetic study of macquarimicins: Highly stereoselective construction of the AB-ring system
Munakata, Ryosuke,Ueki, Tatsuo,Katakai, Hironori,Takao, Ken-Ichi,Tadano, Kin-Ichi
, p. 3029 - 3032 (2007/10/03)
matrix presented The highly stereoselective synthesis of the AB-ring system of macquarimicins, a novel class of microbial metabolites with inhibitory activity for neutral sphingomyelinase, has been achieved. The present synthesis features the highly stere