1165-60-2Relevant academic research and scientific papers
The absolute configuration of angular 3′-acyloxypyranocoumarins by vibrational circular dichroism exciton chirality
Buenda-Trujillo, Abigail I.,Torrres-Valencia, J. Martn,Joseph-Nathan, Pedro,Burgueo-Tapia, Eleuterio
, p. 1418 - 1423 (2015/02/02)
A complex mixture of lomatin C-3′ esters and (-)-O-angeloyllomatin 1 was isolated from the seeds of Prionosciadium thapsoides. Since a literature search revealed that some lomatin C-3′ monoesters have positive specific rotations, while others had negative values, the absolute configuration of all of the molecules was determined to be (R) by exciton chirality in the infrared region, and by chemical correlation. A single crystal X-ray study of acetyllomatin 3, using the Flack and Hooft parameters, independently confirmed this absolute configuration.
Semisynthesis of ingenol 3-angelate (PEP005): Efficient stereoconservative angeloylation of alcohols
Liang, Xifu,Grue-Sorensen, Gunnar,Petersen, Anders Klarskov,H?gberg, Thomas
, p. 2647 - 2652 (2013/01/15)
A high-yielding method was developed for the preparation of ingenol 3-angelate (PEP005, ingenol mebutate) via the corresponding 5,20-acetonide without concomitant isomerization of the angelate (Z-form) to the corresponding tiglate (E-form). The general sc
