133095-58-6Relevant academic research and scientific papers
Palladium catalyzed cyclizations of enantiomerically pure acyclic 4-acetoxy-2,8-nonadienes: Efficient chirality transfer
Oppolzer, Wolfgang,Birkinshaw, Timothy N.,Bernardinelli, Gerald
, p. 6995 - 6998 (1990)
S-4-Acetoxy-6-aza-2,8-nonadienes 9 and 11 were subjected to Pd(0)-catalyzed cyclizations. The S,E-acetate 9 gave exclusively S,E-pyrrolidine 12, whereas the antipodal product R,E-12 was formed from the S,Z-precursor 11 (Scheme 3). X-ray-diffraction analys
First total synthesis of the marine illudalane sesquiterpenoid alcyopterosin E.
Witulski, Bernhard,Zimmermann, Axel,Gowans, Nicholas D
, p. 2984 - 2985 (2007/10/03)
The first synthesis of the marine illudalane sesquiterpenoid alcyopterosin E was accomplished through a concise ABC ring-formation strategy using a rhodium(I)-catalysed intramolecular alkyne cyclotrimerisation as key connection.
