-
3
-
-
0005756906
-
Diterpenoid total synthesis. VIII. (±)-Kaur-16-en-19-oic acid, (±)-kaur-16-en-19-ol, (±)-monogynol and some oxygenated kauranes
-
Mori K, Matsui M,. Diterpenoid total synthesis. VIII. (±)-Kaur-16-en-19-oic acid, (±)-kaur-16-en-19-ol, (±)-monogynol and some oxygenated kauranes. Tetrahedron 1968; 24: 3095-3111.
-
(1968)
Tetrahedron
, vol.24
, pp. 3095-3111
-
-
Mori, K.1
Matsui, M.2
-
4
-
-
1842482394
-
18-Ceropia juvenile hormone
-
18-Ceropia juvenile hormone. Tetrahedron 1972; 28: 3747-3756.
-
(1972)
Tetrahedron
, vol.28
, pp. 3747-3756
-
-
Mori, K.1
-
5
-
-
0007692388
-
Synthesis of compounds with juvenile hormone activity. I. (±)-Juvabione (methyl (±)-todomatuate)
-
Mori K, Matsui M,. Synthesis of compounds with juvenile hormone activity. I. (±)-Juvabione (methyl (±)-todomatuate). Tetrahedron 1968; 24: 3127-3138.
-
(1968)
Tetrahedron
, vol.24
, pp. 3127-3138
-
-
Mori, K.1
Matsui, M.2
-
6
-
-
0001176010
-
Synthesis of optically active grasshopper ketone and dehydrovomifoliol as a synthetic support for the revised absolute configuration of (+)-abscisic acid
-
Mori K,. Synthesis of optically active grasshopper ketone and dehydrovomifoliol as a synthetic support for the revised absolute configuration of (+)-abscisic acid. Tetrahedron 1974; 30: 1065-1072.
-
(1974)
Tetrahedron
, vol.30
, pp. 1065-1072
-
-
Mori, K.1
-
7
-
-
0015886063
-
Absolute configuration of (-)-14-methyl-cis-8-hexadecen-1-ol and methyl (-)-14-methyl-cis-8-hexadecenoate, the sex attractant of female dermestid beetle, Trogoderma inclusum le Conte
-
(full paper: Tetrahedron 1974;30:3817-3820).
-
Mori K,. Absolute configuration of (-)-14-methyl-cis-8-hexadecen-1-ol and methyl (-)-14-methyl-cis-8-hexadecenoate, the sex attractant of female dermestid beetle, Trogoderma inclusum Le Conte. Tetrahedron Lett 1973; 3869-3872 (full paper: Tetrahedron 1974;30:3817-3820).
-
(1973)
Tetrahedron Lett
, pp. 3869-3872
-
-
Mori, K.1
-
8
-
-
0000098071
-
Synthesis of exo-brevicomin, the pheromone of western pine beetle, to obtain optically active forms of known absolute configuration
-
Mori K,. Synthesis of exo-brevicomin, the pheromone of western pine beetle, to obtain optically active forms of known absolute configuration. Tetrahedron 1974; 30: 4223-4227.
-
(1974)
Tetrahedron
, vol.30
, pp. 4223-4227
-
-
Mori, K.1
-
9
-
-
0017115027
-
Western pine beetle: Specificity among enantiomers of male and female components of an attractant pheromone
-
Wood DL, Browne LE, Ewing B, Lindahl K, Bedard WD, Tilden PE, Mori K, Pitman GB, Hughes PR,. Western pine beetle: specificity among enantiomers of male and female components of an attractant pheromone. Science 1976; 192: 896-898.
-
(1976)
Science
, vol.192
, pp. 896-898
-
-
Wood, D.L.1
Browne, L.E.2
Ewing, B.3
Lindahl, K.4
Bedard, W.D.5
Tilden, P.E.6
Mori, K.7
Pitman, G.B.8
Hughes, P.R.9
-
10
-
-
0001603822
-
Synthesis of (1S,5R)-karahana ether and (1S,5R)-karahana lactone, the optically active forms of unique monoterpenes with a 6-oxabicyclo[3.2.1]octane ring system
-
Mori K, Mori H,. Synthesis of (1S,5R)-karahana ether and (1S,5R)-karahana lactone, the optically active forms of unique monoterpenes with a 6-oxabicyclo[3.2.1]octane ring system. Tetrahedron 1985; 41: 5487-5493.
-
(1985)
Tetrahedron
, vol.41
, pp. 5487-5493
-
-
Mori, K.1
Mori, H.2
-
11
-
-
0000570612
-
Synthesis of both the enantiomers of dihydroactinidiolide, a pheromone component of the red imported fire ant
-
Mori K, Nakazono Y,. Synthesis of both the enantiomers of dihydroactinidiolide, a pheromone component of the red imported fire ant. Tetrahedron 1986; 42: 283-290.
-
(1986)
Tetrahedron
, vol.42
, pp. 283-290
-
-
Mori, K.1
Nakazono, Y.2
-
12
-
-
0009487356
-
A natural product was shown to be of low optical purity: Synthesis of (2S,5R,6E,8E)-2,5-epoxy-6,8-megastigmadiene, its (6Z,8E)-isomer and (2S,6R,7S,8E)-2,7-epoxy-4,8-megastigmadiene, the constituents of Osmanthus absolute
-
Mori K, Tamura H,. A natural product was shown to be of low optical purity: synthesis of (2S,5R,6E,8E)-2,5-epoxy-6,8-megastigmadiene, its (6Z,8E)-isomer and (2S,6R,7S,8E)-2,7-epoxy-4,8-megastigmadiene, the constituents of Osmanthus absolute. Tetrahedron 1986; 42: 2643-2646.
-
(1986)
Tetrahedron
, vol.42
, pp. 2643-2646
-
-
Mori, K.1
Tamura, H.2
-
13
-
-
37049067095
-
Triterpenoid total synthesis. III. Synthesis of meso- and (±)-limatulone, defensive metabolites of the limpet Collisella limatula
-
Mori K, Takikawa H, Kido M,. Triterpenoid total synthesis. III. Synthesis of meso- and (±)-limatulone, defensive metabolites of the limpet Collisella limatula. J Chem Soc Perkin Trans 1 1993; 169-179.
-
(1993)
J Chem Soc Perkin Trans 1
, pp. 169-179
-
-
Mori, K.1
Takikawa, H.2
Kido, M.3
-
14
-
-
0000211760
-
Synthesis of (6S,1′S)-(+)-hernandulcin, a sweetener, and its stereoisomers
-
Mori K, Kato M,. Synthesis of (6S,1′S)-(+)-hernandulcin, a sweetener, and its stereoisomers. Tetrahedron 1986; 21: 5895-5900.
-
(1986)
Tetrahedron
, vol.21
, pp. 5895-5900
-
-
Mori, K.1
Kato, M.2
-
15
-
-
0025058527
-
Biological activity of enantiomerically pure forms of insect juvenile hormone i and III in Bombyx mori
-
Sakurai S, Ohtaki T, Mori H, Fujiwhara M, Mori K,. Biological activity of enantiomerically pure forms of insect juvenile hormone I and III in Bombyx mori. Experientia 1990; 46: 220-221.
-
(1990)
Experientia
, vol.46
, pp. 220-221
-
-
Sakurai, S.1
Ohtaki, T.2
Mori, H.3
Fujiwhara, M.4
Mori, K.5
-
16
-
-
0342848627
-
Relationship between the absolute configuration and the biological activity of juvenile hormone III
-
Kindle H, Winistarfer M, Lanzrein B, Mori K,. Relationship between the absolute configuration and the biological activity of juvenile hormone III. Experientia 1989; 45: 356-360.
-
(1989)
Experientia
, vol.45
, pp. 356-360
-
-
Kindle, H.1
Winistarfer, M.2
Lanzrein, B.3
Mori, K.4
-
17
-
-
0016620990
-
Synthesis of optically active forms of sulcatol, the aggregation pheromone in the scolytid beetle Gnathotrichus sulcatus
-
Mori K,. Synthesis of optically active forms of sulcatol, the aggregation pheromone in the scolytid beetle Gnathotrichus sulcatus. Tetrahedron 1975; 31: 3011-3012.
-
(1975)
Tetrahedron
, vol.31
, pp. 3011-3012
-
-
Mori, K.1
-
18
-
-
0017065990
-
Gnathotrichus sulcatus: Synergistic response to enantiomers of the aggregation pheromone sulcatol
-
Borden JH, Chong L, McLean JA, Slessor KN, Mori K,. Gnathotrichus sulcatus: synergistic response to enantiomers of the aggregation pheromone sulcatol. Science 1976; 192: 894-896.
-
(1976)
Science
, vol.192
, pp. 894-896
-
-
Borden, J.H.1
Chong, L.2
McLean, J.A.3
Slessor, K.N.4
Mori, K.5
-
19
-
-
0017191869
-
Stereoselective synthesis of optically active disparlure, the pheromone of the gypsy moth
-
(full paper: Tetrahedron 1979;35:833-837).
-
Mori K, Takigawa T, Matsui M,. Stereoselective synthesis of optically active disparlure, the pheromone of the gypsy moth. Tetrahedron Lett 1976: 3953-3956 (full paper: Tetrahedron 1979;35:833-837).
-
(1976)
Tetrahedron Lett
, pp. 3953-3956
-
-
Mori, K.1
Takigawa, T.2
Matsui, M.3
-
20
-
-
0017088938
-
Chirality of insect pheromones: Response interruption by inactive antipode
-
Vité JP, Klimetzek D, Loskant G, Hedden R, Mori K,. Chirality of insect pheromones: response interruption by inactive antipode. Naturwissenschaften 1976; 63: 582-583.
-
(1976)
Naturwissenschaften
, vol.63
, pp. 582-583
-
-
Vité, J.P.1
Klimetzek, D.2
Loskant, G.3
Hedden, R.4
Mori, K.5
-
21
-
-
0001144298
-
Gypsy moth field trapping and electroantennogram studies with pheromone enantiomers
-
Miller JG, Mori K, Roelofs WL,. Gypsy moth field trapping and electroantennogram studies with pheromone enantiomers. J Insect Physiol 1977; 23: 1447-1454.
-
(1977)
J Insect Physiol
, vol.23
, pp. 1447-1454
-
-
Miller, J.G.1
Mori, K.2
Roelofs, W.L.3
-
22
-
-
0019418795
-
Stereocontrolled synthesis of all of the possible stereoisomers of 3,11-dimethylnonacosan-2-one and 29-hydroxy-3,11-dimethylnonacosan-2-one. The female sex pheromone of the German cockroach
-
DOI 10.1016/S0040-4020(01)92448-2
-
Mori K, Masuda S, Suguro T,. Stereocontrolled synthesis of all of the possible stereoisomers of 3,11-dimethylnonacosan-2-one and 29-hydroxy-3,11- dimethylnonacosan-2-one, the female sex pheromone of the German cockroach. Tetrahedron 1981; 37: 1329-1340. (Pubitemid 11075833)
-
(1981)
Tetrahedron
, vol.37
, Issue.7
, pp. 1329-1340
-
-
Mori, K.1
Masuda, S.2
Suguro, T.3
-
23
-
-
0010561144
-
A new synthesis of the four stereoisomers of 3,11-dimethyl-2- nonacosanone, the female-produced sex pheromone of the German cockroach
-
Mori K, Takikawa H,. A new synthesis of the four stereoisomers of 3,11-dimethyl-2-nonacosanone, the female-produced sex pheromone of the German cockroach. Tetrahedron 1990; 46: 4473-4486.
-
(1990)
Tetrahedron
, vol.46
, pp. 4473-4486
-
-
Mori, K.1
Takikawa, H.2
-
24
-
-
40849094155
-
Synthesis of all the six components of the female-produced contact sex pheromone of the German cockroach, Blattella germanica (L)
-
Mori K,. Synthesis of all the six components of the female-produced contact sex pheromone of the German cockroach, Blattella germanica (L). Tetrahedron 2008; 64: 4060-4071.
-
(2008)
Tetrahedron
, vol.64
, pp. 4060-4071
-
-
Mori, K.1
-
25
-
-
4844223258
-
Behavioral activity of stereoisomers and a new component of the contact sex pheromone of female german cockroach, Blattella germanica
-
DOI 10.1023/B:JOEC.0000042405.05895.3a
-
Eliyahu D, Mori K, Takikawa H, Leal WS, Schal C,. Behavioral activity of stereoisomers and new component of the contact sex pheromone of female German cockroach, Blattella germanica. J Chem Ecol 2004; 30: 1839-1848. (Pubitemid 39318597)
-
(2004)
Journal of Chemical Ecology
, vol.30
, Issue.9
, pp. 1839-1848
-
-
Eliyahu, D.1
Mori, K.2
Takikawa, H.3
Leal, W.S.4
Schal, C.5
-
26
-
-
0001683960
-
Synthesis of the optically active forms of 4,10-dihydroxy-1,7- dioxaspiro[5.5]undecane and their conversion to the enantiomers of 1,7-dioxaspiro[5.5]undecane, the olive fruit fly pheromone
-
Mori K, Uematsu T, Yanagi K, Minobe M,. Synthesis of the optically active forms of 4,10-dihydroxy-1,7-dioxaspiro[5.5]undecane and their conversion to the enantiomers of 1,7-dioxaspiro[5.5]undecane, the olive fruit fly pheromone. Tetrahedron 1985; 41: 2751-2758.
-
(1985)
Tetrahedron
, vol.41
, pp. 2751-2758
-
-
Mori, K.1
Uematsu, T.2
Yanagi, K.3
Minobe, M.4
-
27
-
-
0000730590
-
Synthesis of the enantiomers of 1,7-dioxaspiro[5.5]undecane, 4-hydroxy-1,7-dioxaspiro[5.5]undecane and 3-hydroxy-1,7-dioxaspiro[5.5]undecane, the components of the olive fruit fly pheromone
-
Mori K, Watanabe H, Yanagi K, Minobe M,. Synthesis of the enantiomers of 1,7-dioxaspiro[5.5]undecane, 4-hydroxy-1,7-dioxaspiro[5.5]undecane and 3-hydroxy-1,7-dioxaspiro[5.5]undecane, the components of the olive fruit fly pheromone. Tetrahedron 1985; 41: 3663-3672.
-
(1985)
Tetrahedron
, vol.41
, pp. 3663-3672
-
-
Mori, K.1
Watanabe, H.2
Yanagi, K.3
Minobe, M.4
-
28
-
-
0000757387
-
Sex-specific activity of (R)-(-)- and (S)-(+)-1,7-dioxaspiro[5.5] undecane, 4-hydroxy-1,7-dioxaspiro[5.5]undecane and 3-hydroxy-1,7-dioxaspiro[5. 5]undecane, the major pheromone of Dacus oleae
-
Haniotakis G, Francke W, Mori K, Redlich H, Schurig V,. Sex-specific activity of (R)-(-)- and (S)-(+)-1,7-dioxaspiro[5.5]undecane, 4-hydroxy-1,7-dioxaspiro[5.5]undecane and 3-hydroxy-1,7-dioxaspiro[5.5]undecane, the major pheromone of Dacus oleae. J Chem Ecol 1986; 12: 1559-1568.
-
(1986)
J Chem Ecol
, vol.12
, pp. 1559-1568
-
-
Haniotakis, G.1
Francke, W.2
Mori, K.3
Redlich, H.4
Schurig, V.5
-
29
-
-
85055474993
-
Chemoenzymatic preparation of enantiopure building blocks of synthetic utility
-
In: Patel R.N., editor. Boca Raton: CRC Press;. p.
-
Mori K,. Chemoenzymatic preparation of enantiopure building blocks of synthetic utility. In:, Patel RN, editor. Biocatalysis in the pharmaceutical and biotechnology industries. Boca Raton: CRC Press; 2007. p 563-589.
-
(2007)
Biocatalysis in the Pharmaceutical and Biotechnology Industries
, pp. 563-589
-
-
Mori, K.1
-
30
-
-
0012355554
-
Yeast reduction of 2,2-dimethylcyclohexane-1,3-dione: (S)-3-hydroxy-2,2-dimethylcyclohexanone
-
Mori K, Mori H,. Yeast reduction of 2,2-dimethylcyclohexane-1,3-dione: (S)-3-hydroxy-2,2-dimethylcyclohexanone. Org Synth Coll Vol. 1993; 8: 312-315.
-
(1993)
Org Synth Coll Vol.
, vol.8
, pp. 312-315
-
-
Mori, K.1
Mori, H.2
-
31
-
-
0026673473
-
Enzymatic preparation of (2S,3R)-4-acetoxy-2,3-epoxybutan-1-ol and its conversion to the epoxy pheromones of the gypsy moth and the ruby tiger moth
-
Brevet J-L, Mori K,. Enzymatic preparation of (2S,3R)-4-acetoxy-2,3- epoxybutan-1-ol and its conversion to the epoxy pheromones of the gypsy moth and the ruby tiger moth. Synthesis 1992; 1007-1012.
-
(1992)
Synthesis
, pp. 1007-1012
-
-
Brevet, J.-L.1
Mori, K.2
-
32
-
-
0037395147
-
Synthesis of all four stereoisomers of leucomalure, components of the female sex pheromone of the satin moth, Leucoma salicis
-
Muto S, Mori K,. Synthesis of all four stereoisomers of leucomalure, components of the female sex pheromone of the satin moth, Leucoma salicis. Eur J Org Chem 2003; 1300-1307.
-
(2003)
Eur J Org Chem
, pp. 1300-1307
-
-
Muto, S.1
Mori, K.2
-
33
-
-
77649192025
-
Pheromone synthesis, Part 243: Synthesis and biological evaluation of (3R,13R,1′S)-1′-ethyl-2′-methylpropyl 3,13- dimethylpentadecanoate, the major component of the sex pheromone of Paulownia bagworm, Clania variegata, and its stereoisomers
-
Mori K, Tashiro T, Zhao B, Suckling DM, El-Sayed AM,. Pheromone synthesis, Part 243: synthesis and biological evaluation of (3R,13R,1′S)- 1′-ethyl-2′-methylpropyl 3,13-dimethylpentadecanoate, the major component of the sex pheromone of Paulownia bagworm, Clania variegata, and its stereoisomers. Tetrahedron 2010; 66: 2642-2653.
-
(2010)
Tetrahedron
, vol.66
, pp. 2642-2653
-
-
Mori, K.1
Tashiro, T.2
Zhao, B.3
Suckling, D.M.4
El-Sayed, A.M.5
-
34
-
-
77955432325
-
Pheromone synthesis, Part 244: Synthesis of the racemate and enantiomers of (11Z,19Z)-CH503 (3-acetoxy-11,19-octacosadien-1-ol), a new sex pheromone of male Drosophila melanogaster to show its (S)-isomer and racemate as bioactive
-
Mori K, Shikichi Y, Shankar S, Yew JY,. Pheromone synthesis, Part 244: synthesis of the racemate and enantiomers of (11Z,19Z)-CH503 (3-acetoxy-11,19-octacosadien-1-ol), a new sex pheromone of male Drosophila melanogaster to show its (S)-isomer and racemate as bioactive. Tetrahedron 2010; 66: 7161-7168.
-
(2010)
Tetrahedron
, vol.66
, pp. 7161-7168
-
-
Mori, K.1
Shikichi, Y.2
Shankar, S.3
Yew, J.Y.4
-
35
-
-
35348815718
-
Significance of chirality in pheromone science
-
DOI 10.1016/j.bmc.2007.08.040, PII S0968089607007432
-
Mori K,. Significance of chirality in pheromone science. Bioorg Med Chem 2007; 15: 7505-7523. (Pubitemid 47575904)
-
(2007)
Bioorganic and Medicinal Chemistry
, vol.15
, Issue.24
, pp. 7505-7523
-
-
Mori, K.1
|