1035455-36-7Relevant academic research and scientific papers
A concise stereoselective formal total synthesis of the cytotoxic macrolide (+)-Neopeltolide via Prins cyclization
Yadav, Jhillu Singh,Krishana, Gunda Gopala,Kumar, Satya Narayana
experimental part, p. 480 - 487 (2010/03/03)
A convergent and highly stereoselective formal total synthesis of the naturally occurring, cytotoxic 14-membered macrolide neopeltolide has been achieved via two Prins cyclizations.
Total synthesis of (+)-neopeltolide by a Prins macrocyclization
Woo, Sang Kook,Kwon, Min Sang,Lee, Eun
, p. 3242 - 3244 (2008/12/23)
(Chemical Equation Presented) Rings within rings: The total synthesis of (+)-neopeltolide was accomplished by employing an intramolecular Prins macrocyclization of an aldehydic homoallylic alcohol intermediate (see scheme).
