191212-52-9Relevant academic research and scientific papers
Total synthesis of (-)-sporochnol A, the fish deterrent, from a chiral malonate
Fadel, Antoine,Vandromme, Lucie
, p. 1153 - 1162 (2007/10/03)
From a single chiron, the homochiral benzylic malonic acid ester (R)- (+)-2 available with high enantiomeric excess by enzymatic hydrolysis (PLE acetonic powder), enantiomerically pure (-)-sporochnol A 1 was prepared. This versatile method allows preparation of sporochnol 1, via aldehydes 7 and 15, in good overall yield.
The absolute configuration of (+)-sporochnol A, the fish deterrent from the Caribbean marine alga Sporochnus bolleanus
Takahashi, Michiyasu,Shioura, Yoko,Murakami, Taku,Ogasawara, Kunio
, p. 1235 - 1242 (2007/10/03)
The absolute configuration of (+)-sporochnol A, the fish deterrent from the Caribbean marine alga Sporochnus bolleanus, has been established as S based on the stereocontrolled synthesis of its (R)-(-)-enantiomer from (S)-epichlorohydrin.
