112494-44-7Relevant academic research and scientific papers
An Efficient Stereoselective Total Synthesis of Bioactive (3R,5R)-1-(4-Hydroxyphenyl)-7-phenylheptane-3,5-diol via Asymmetric Aldol Reaction
Ramesh, Perla,Raju, Atla,Fadnavis, Nitin W.
, p. 70 - 72 (2016/01/26)
An efficient stereoselective total synthesis of (3R,5R)-1-(4-hydroxyphenyl)-7-phenylheptane-3,5-diol (1) is reported based on the Mukaiyama aldol reaction. The total synthesis of compound 1 was accomplished with 30% overall yield in simple eight steps from commercially available trans-cinnamaldehyde.
The first stereoselective total synthesis of naturally occurring, bioactive (3R,5R)-1-(4-hydroxyphenyl)-7-phenylheptane-3,5-diol and the synthesis of its enantiomer
Reddy, Parigi Raghavendar,Sudhakar, Chithaluri,Kumar, Jayprakash Narayan,Das, Biswanath
, p. 289 - 295 (2013/03/28)
The first stereoselective total synthesis of the naturally occurring anti-emetic diarylheptanoid (3R,5R)-1-(4-hydroxyphenyl)-7-phenylheptane-3,5-diol (1) was accomplished starting from 4-hydroxybenzaldehyde and involving a Sharpless kinetic resolution and
