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Results: 1-12 |
Results: 12
Use of odorless thiols: Formal asymmetric Michael addition of hydrogen sulfide to alpha-substituted alpha,beta-unsaturated carbonyl compounds
Authors: Nishide, K Ohsugi, S Shiraki, H Tamakita, H Node, M
Citation: K. Nishide et al., Use of odorless thiols: Formal asymmetric Michael addition of hydrogen sulfide to alpha-substituted alpha,beta-unsaturated carbonyl compounds, ORG LETT, 3(20), 2001, pp. 3121-3124
An efficient synthesis of (+/-)-narwedine and (+/-)-galanthamine by an improved phenolic oxidative coupling
Authors: Node, M Kodama, S Hamashima, Y Baba, T Hamamichi, N Nishide, K
Citation: M. Node et al., An efficient synthesis of (+/-)-narwedine and (+/-)-galanthamine by an improved phenolic oxidative coupling, ANGEW CHEM, 40(16), 2001, pp. 3060-3062
A novel intramolecular through-space interaction between F and CN: a strategy for the conformational control of an acyclic system
Authors: Nishide, K Hagimoto, Y Hasegawa, H Shiro, M Node, M
Citation: K. Nishide et al., A novel intramolecular through-space interaction between F and CN: a strategy for the conformational control of an acyclic system, CHEM COMMUN, (22), 2001, pp. 2394-2395
A species-selective allelopathic substance from germinating sunflower (Helianthus annuus L.) seeds
Authors: Ohno, S Tomita-Yokotani, K Kosemura, S Node, M Suzuki, T Amano, M Yasui, K Goto, T Yamamura, S Hasegawa, K
Citation: S. Ohno et al., A species-selective allelopathic substance from germinating sunflower (Helianthus annuus L.) seeds, PHYTOCHEM, 56(6), 2001, pp. 577-581
An asymmetric total synthesis of a potent immunosuppressant, mycestericinsD and F, through an aldol reaction using L-threonine aldolase
Authors: Nishide, K Shibata, K Fujita, T Kajimoto, T Wong, CH Node, M
Citation: K. Nishide et al., An asymmetric total synthesis of a potent immunosuppressant, mycestericinsD and F, through an aldol reaction using L-threonine aldolase, HETEROCYCLE, 52(3), 2000, pp. 1191
A novel tandem [4(+)+2] cycloaddition-elimination reaction of 4,4-dimethyl-2-styryl-1,3-oxathianes with olefins
Authors: Nishide, K Ohsugi, S Node, M
Citation: K. Nishide et al., A novel tandem [4(+)+2] cycloaddition-elimination reaction of 4,4-dimethyl-2-styryl-1,3-oxathianes with olefins, TETRAHEDR L, 41(3), 2000, pp. 371-375
Highly enantioselective synthesis of 1,3-mercapto alcohols from alpha,beta-unsaturated ketones: asymmetric bifunctional group exchange reaction
Authors: Shiraki, H Nishide, K Node, M
Citation: H. Shiraki et al., Highly enantioselective synthesis of 1,3-mercapto alcohols from alpha,beta-unsaturated ketones: asymmetric bifunctional group exchange reaction, TETRAHEDR L, 41(18), 2000, pp. 3437-3441
Hinokitiol, a selective inhibitor of the platelet-type isozyme of arachidonate 12-lipoxygenase
Authors: Suzuki, H Ueda, T Juranek, I Yamamoto, S Katoh, T Node, M Suzuki, T
Citation: H. Suzuki et al., Hinokitiol, a selective inhibitor of the platelet-type isozyme of arachidonate 12-lipoxygenase, BIOC BIOP R, 275(3), 2000, pp. 885-889
A novel tandem Michael addition/Meerwein-Ponndorf-Verley reduction: Asymmetric reduction of acyclic alpha,beta-unsaturated ketones using a chiral mercapto alcohol
Authors: Node, M Nishide, K Shigeta, Y Shiraki, H Obata, K
Citation: M. Node et al., A novel tandem Michael addition/Meerwein-Ponndorf-Verley reduction: Asymmetric reduction of acyclic alpha,beta-unsaturated ketones using a chiral mercapto alcohol, J AM CHEM S, 122(9), 2000, pp. 1927-1936
A new divergent asymmetric synthesis of (+)- and (-)-ethosuximides and their anti-convulsant activities
Authors: Katoh, T Nishide, K Node, M Ogura, H
Citation: T. Katoh et al., A new divergent asymmetric synthesis of (+)- and (-)-ethosuximides and their anti-convulsant activities, HETEROCYCLE, 50(2), 1999, pp. 833-841
Synthesis and anti-influenza virus activity of novel pyrimidine derivatives
Authors: Hisaki, M Imabori, H Azuma, M Suzutani, T Iwakura, F Ohta, Y Kawanishi, K Ichigobara, Y Node, M Nishide, K Yoshida, I Ogasawara, M
Citation: M. Hisaki et al., Synthesis and anti-influenza virus activity of novel pyrimidine derivatives, ANTIVIR RES, 42(2), 1999, pp. 121-137
Novel asymmetric dealkoxycarbonylation of 3-oxo-8-azabicyclo[3.2.1]octane-2,4-dicarboxylates using porcine liver esterase: A new route to (-)-anhydroecgonine methyl ester
Authors: Node, M Nakamura, S Nakamura, D Katoh, T Nishide, K
Citation: M. Node et al., Novel asymmetric dealkoxycarbonylation of 3-oxo-8-azabicyclo[3.2.1]octane-2,4-dicarboxylates using porcine liver esterase: A new route to (-)-anhydroecgonine methyl ester, TETRAHEDR L, 40(29), 1999, pp. 5357-5360
Risultati: 1-12 |