671798-21-3Relevant articles and documents
Stereoselective total synthesis of Oxylipins: (6S,7E,9R,10S)-6,9,10- trihydroxyoctadec-7-enoic acid and (6z,8r,9r,10s)-8,9,10-trihydroxyoctadec-6- enoic acid
Singh Yadav, Jhillu,Shiva Shankar, Kattela,Srinivas Reddy, Anugu,Subba Reddy, Basi V.
, p. 546 - 555 (2014/05/06)
The stereoselective total syntheses of oxylipins 1b and 1c are described starting from readily accessible natural sugars via the Grubbs cross-metathesis, Wittig olefination, and Zn-mediated reductive elimination as key steps. Copyright
Synthesis of fused bicyclic glutarimides
Chang, Meng-Yang,Chen, Chung-Yi,Chen, Shui-Tein,Chang, Nein-Chen
, p. 7547 - 7553 (2007/10/03)
We describe an efficient route towards the synthesis of fused bicyclic glutarimides using facile [3+3] reaction of α-sulfonylacetamides with different α,β-unsaturated esters as the key step. Intramolecular cyclization of 4-substituted 3-sulfonylglutarimide to form 5,6-, 6,6- or 6,7-fused bicyclic glutarimides was accomplished via alkylation, oxidative cyclization or ring-closing metathesis in modest yield.