1-Arylnaphthalene lignan lactones were synthesized in good yields from O-(tert-butyldimethylsilyl)cyanohydrins in two steps based on a conjugate addition-aldol reaction, followed by acid-catalyzed closure to form the naphthalene ring. 4-Hydroxy-1-arylnaphthalene lignan lactones were also synthesized by conjugate addition-aldol reaction, followed by aromatization-lactonization.
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TAISHO PHARMACEUT CO LTD, RES CTR, DEPT PHARMACOL, OMIYA, SAITAMA 330, JAPANTAISHO PHARMACEUT CO LTD, RES CTR, DEPT PHARMACOL, OMIYA, SAITAMA 330, JAPAN
HIBINO, S
SUGINO, E
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TAISHO PHARMACEUT CO LTD, RES CTR, DEPT PHARMACOL, OMIYA, SAITAMA 330, JAPANTAISHO PHARMACEUT CO LTD, RES CTR, DEPT PHARMACOL, OMIYA, SAITAMA 330, JAPAN
SUGINO, E
YAMOCHI, T
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TAISHO PHARMACEUT CO LTD, RES CTR, DEPT PHARMACOL, OMIYA, SAITAMA 330, JAPANTAISHO PHARMACEUT CO LTD, RES CTR, DEPT PHARMACOL, OMIYA, SAITAMA 330, JAPAN
YAMOCHI, T
KUWATA, M
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TAISHO PHARMACEUT CO LTD, RES CTR, DEPT PHARMACOL, OMIYA, SAITAMA 330, JAPANTAISHO PHARMACEUT CO LTD, RES CTR, DEPT PHARMACOL, OMIYA, SAITAMA 330, JAPAN
KUWATA, M
HASHIMOTO, H
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TAISHO PHARMACEUT CO LTD, RES CTR, DEPT PHARMACOL, OMIYA, SAITAMA 330, JAPANTAISHO PHARMACEUT CO LTD, RES CTR, DEPT PHARMACOL, OMIYA, SAITAMA 330, JAPAN
HASHIMOTO, H
SATO, K
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TAISHO PHARMACEUT CO LTD, RES CTR, DEPT PHARMACOL, OMIYA, SAITAMA 330, JAPANTAISHO PHARMACEUT CO LTD, RES CTR, DEPT PHARMACOL, OMIYA, SAITAMA 330, JAPAN
SATO, K
AMANUMA, F
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TAISHO PHARMACEUT CO LTD, RES CTR, DEPT PHARMACOL, OMIYA, SAITAMA 330, JAPANTAISHO PHARMACEUT CO LTD, RES CTR, DEPT PHARMACOL, OMIYA, SAITAMA 330, JAPAN
AMANUMA, F
KARASAWA, Y
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TAISHO PHARMACEUT CO LTD, RES CTR, DEPT PHARMACOL, OMIYA, SAITAMA 330, JAPANTAISHO PHARMACEUT CO LTD, RES CTR, DEPT PHARMACOL, OMIYA, SAITAMA 330, JAPAN