Chemistry Letters p. 845 - 846 (1997)
Update date:2022-08-03
Topics:
Oishi, Tohru
Shoji, Mitsuru
Kumahara, Naomi
Hirama, Masahiro
Stereoselective synthesis of the LM ring moiety of ciguatoxin was achieved from (R)-(E)-1-benzyloxy-2-hydroxy-3-pentene via Ireland-Claisen rearrangement, iodolactonization, and reagent-controlled asymmetric dihydroxylation.
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Doi:10.1016/S0040-4020(97)00545-0
(1997)Doi:10.1080/07328309808002333
(1998)Doi:10.1021/ja01040a025
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(2021)Doi:10.1021/jo9709615
(1997)Doi:10.1055/s-1997-983
(1997)
