548483-78-9Relevant academic research and scientific papers
Efficient asymmetric syntheses of (+)-strictifolione
Enders, Dieter,Lenzen, Achim,Müller, Michael
, p. 1486 - 1496 (2007/10/03)
The asymmetric synthesis and a formal asymmetric synthesis of (+)-strictifolione are described. As key step in both approaches the Julia-Kocienski olefination to create an E-configured alkene was used. The anti-1,3-diol moiety was synthesized by employing
Total synthesis of (+)-strictifolione.
BouzBouz, Samir,Cossy, Janine
, p. 1995 - 1997 (2007/10/03)
[reaction: see text] The synthesis of (+)-strictifolione was achieved from 3-phenylproprionaldehyde by using enantioselective allyltitanations to control the stereogenic centers at C6, C4', and C6' and a cross-methathesis to control the configuration of t
