146983-20-2Relevant academic research and scientific papers
Diastereoselective synthesis of the top half of kijanolide
Roush,Brown
, p. 7309 - 7312 (1989)
A highly diastereoselective synthesis of the top half (4) of kijanolide is described. The key step is the exo and diastereoface selective Diels-Alder reaction of triene 6 and chiral dienophile 6.
Indium-mediated allylation of carbonyl compounds with an allylic bromide in aqueous media: Anomalous syn-diastereoselectivity regardless of allylic bromide geometry
Loh, Teck-Peng,Yin, Zheng,Song, Hong-Yan,Tan, Kee-Leng
, p. 911 - 914 (2007/10/03)
Anomalous syn-diastereoselectivity of indium-mediated coupling of aldehydes with bromides Z-3b and E-3b is reported. The reaction afforded high syn selectivity regardless of the allylic bromide geometry. Preliminary studies on the enantioselective indium-mediated allylation were attempted and found to give the desired products in moderate yield with high syn selectivity and enantioselectivity.
A Highly Diastereo- and Enantioselective Synthesis of the Top Half of Kijanolide
Roush, William R.,Brown, Bradley B.
, p. 2151 - 2161 (2007/10/02)
A highly diastereo- and enantioselective synthesis of spirotetronate 4 corresponding to the top half of kijanolide is reported.This synthesis features the novel exo-selective Diels-Alder reaction of triene 6 and the chiral, nonracemic dienophiles (R)-7 an
