Tetrahedron

Synthesis of both enantiomers of hiburipyranone

K Uchida, H Watanabe, T Kitahara

Index: Uchida, Kanako; Watanabe, Hidenori; Kitahara, Takeshi Tetrahedron, 1998 , vol. 54, # 31 p. 8975 - 8984

Full Text: HTML

Citation Number: 26

Abstract

Download full text in PDF Opens in a new window. Article suggestions will be shown in a dialog on return to ScienceDirect. ... Please enable JavaScript to use all the features on this page. ... Both enentiomers of hiburipyranone, a cytotoxic metabolite of marine sponge, was synthesized employing Sharpless' asymmetric dihydroxylation as a key step and absolute configuration of the natural compound at C-3 position was determined to be R. ... Both enantiomers of ...

 Related Synthetic Route
N/A Structure

212757-55-6

N/A

~0%

1,3-Dimethoxy-5-pentylbenzene Structure

22976-40-5

1,3-Dimethoxy-5...

N/A Structure

212757-56-7

N/A

(4R,5R)-4-(3,5-dimethoxyphenyl)-5-propyl-1,3-dioxolane-2-thione Structure

212757-44-3

(4R,5R)-4-(3,5-...

~0%

1,3-Dimethoxy-5-pentylbenzene Structure

22976-40-5

1,3-Dimethoxy-5...

(R)-1-(3,5-dimethoxyphenyl)-2-pentanol Structure

212757-45-4

(R)-1-(3,5-dime...


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