107673-74-5Relevant articles and documents
Stereocontrolled photooxygenations - A valuable synthetic tool
Adam, Waldemar,Saha-Moeller, Chantu R.,Schambony, Simon B.,Schmid, Katharina S.,Wirth, Thomas
, p. 476 - 483 (2007/10/03)
The stereochemical course of the singlet-oxygen ene reaction with acyclic olefins may be controlled if in the substrate conformational fixation (1,3-allylic strain) an allylic substituent for interaction with the attacking oxygen enophile aligns. Various
Synthesis and Structure Elucidation of Merucathine and Pseudomerucathine. Two Constituents of Catha edulis FORSK.
Wolf, Jean-Pierre,Pfander, Hanspeter
, p. 918 - 926 (2007/10/02)
Starting from L-alanine, two constituents of Catha edulis FORSK. (3R,4S)-4-amino-1-phenyl-1-penten-3-ol ((3R,4S)-4, merucathine) and (3S,4S)-4-amino-1-phenyl-1-penten-3-ol ((3S,4S)-4, pseudomerucathine) were synthesized.