700367-90-4Relevant academic research and scientific papers
Total synthesis of haliclamide
Gahalawat, Suraksha,Pandey, Satyendra Kumar
supporting information, p. 9287 - 9293 (2016/10/13)
A stereoselective approach for the synthesis of haliclamide 1, a marine natural product, has been developed. The notable features of our synthesis include MacMillan cross aldol, Mitsunobu inversion, Yamaguchi-Hirao alkylation, Steglich esterification and
An unprecedented silver salt effect switches the facial selectivity in the vinylogous mukaiyama aldol reaction
Liang, Yufan,Wang, Lin,Zhu, Rong,Deng, Lujiang,Yang, Yunfang,Quan, Junmin,Chen, Jiahua,Yang, Zhen
supporting information; experimental part, p. 2387 - 2393 (2011/02/22)
Silver hexafluroantimonate was identified as a highly efficient agent to reverse the facial selectivity of the titanium chloride-mediated vinylogous Mukaiyama aldol reaction (VMAR), and this unprecedented reaction provides a concise, diastereoselective sy
TOTAL SYNTHESIS OF ( plus )-PHYLLANTHOCIN.
Williams,Sit
, p. 2949 - 2954 (2007/12/18)
Investigations culminating in the total synthesis of ( plus )-phyllanthocin via a highly convergent route beginning with natural tartaric acid are reported. The stereochemical consequences of internal spiroketalization with protic acid and Lewis acid chel
