113219-30-0Relevant articles and documents
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 highly substituted tetrahydropyrans: Preparation of the C20-C28 moiety of phorboxazoles
Chakraborty, Tushar K.,Reddy, V. Ramakrishna,Reddy, T. Jagadeshwar
, p. 8613 - 8622 (2007/10/03)
A propionate-derived polyketide building block A whose 2-methyl-1,3-diol moiety was built by a Ti(III)-mediated ring opening reaction of a trisubstituted 2,3-epoxy alcohol precursor was employed as a common starting material for the syntheses of highly su