224636-41-3Relevant academic research and scientific papers
Establishment of absolute stereostructure of falcarindiol, algicidal principle against Heterocapsa circularisquama from Notopterygii Rhizoma
Tamura, Satoru,Ohno, Tomomichi,Hattori, Yuuhi,Murakami, Nobutoshi
scheme or table, p. 1523 - 1525 (2010/04/29)
Falcarindiol (1) was isolated as an algicidal principle against the harmful red tide dinoflagellate, Heterocapsa circularisquama, from Notopterygii Rhizoma through bioassay-guided separation. In order to determine the ambiguous absolute structure of this
Stereoselective total synthesis of (3R,8S)-falcarindiol, a common polyacetylenic compound from umbellifers
Zheng, Guangrong,Lu, Wei,Cai, Junchao
, p. 626 - 628 (2007/10/03)
The first stereoselective total synthesis of (3R,8S)-falcarindiol (1) from L-tartaric acid and D-xylose is reported, via the Cadiot-Chodkiczwicz reaction, to couple 1-bromoalkyne (2) with 3(R)-(tert-butyldiphenylsilyloxy)- 1-penten-4-yne (3).
