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| Mori, 1981f | Mori, K., H. Nomi, T. Chuman, M. Kohno, K. Kato and M. Noguchi, 1981f. Determination of the absolute configuration at C-6 and C-7 of serricornin (4,6-dimethyl-7-hydroxy-3-nonanone), the sex pheromone of the cigarette beetle. Tetrahedron Lett., 22: 1127–1130. |
| Mori, 1982a | Mori, K. , S. Kuwahara, H. Z. Levinson and A. R. Levinson, 1982a. Synthesis and biological activity of both (E)- and (Z)- isomers of optically pure (S)-14-methyl-8-hexadecenal (trogodermal), the antipodes of the pheromone of the Khapra Beetle. Tetrahedron, 38: 2291–2297. |
| Mori, 1982b | Mori, K. , T. Uematsu, M. Minobe and K. Yanagi, 1982b Synthesis and absolute configuration of (+)-lineatin, the pheromone of Tripodendron lineatum. Tetrahedron Lett. , 23: 1921–1924. |
| Mori, 1982c | Mori, K. and S. Kuwahara, 1982c. Synthesis of optically active forms of (E)-6-isopropyl-3, 9-dimethyl-5, 8-decadienyl acetate, the pheromone of the yellow scale. Tetrahedron, 38: 521–525. |
| Mori, 1982d | Mori, K., H. Nomi, T. Chuman, M. Kohno, K. Kato and M. Noguchi, 1982d. Synthesis and absolute stereochemistry of serricornin [(4S,6S,7S)-4,6-dimethyl-7-hydroxy-3-nonanone], the sex pheromone of the cigarette beetle. Tetrahedron, 38: 3705–3711. |
| Mori, 1983a | Mori, K. , S. Kuwahara and H. Ueda, 1983a. Synthesis of all of the four possible stereoisomers of 4, 8-dimethyldecanal, the aggregation pheromone of the flour beetles. Tetrahedron, 39: 2439–2444. |
| Mori, 1983b | Mori, K. and T. Otsuka, 1983b. Synthesis of both the enantiomers of erythro-6-acetoxy-5-hexadecanolide. Tetrahedron, 39: 3267–3269. |
| Mori, 1984 | Mori, K. and H. Watanabe, 1984. Synthesis of the propionoates of (2R, 8R)- and (2S, 8R)-8-methyl-2-decanol, the pheromone of the western corn rootworm, employing chiral compounds of microbial origin as starting materials. Tetrahedron, 40: 299–303. |
| Mori, 1985a | Mori, K. , M. Kato and S. Kuwahara, 1985a. Pheromone syntheses. LXXIII. New synthesis of (4R, 8R)-4, 8-dimethyldecanal, the aggregation pheromone of Tribolium castaneum, and its (4R, 8S)-isomer. Liebigs Ann. Chem. , 1985: 861–865. |
| Mori, 1985b | Mori, K. and T. Otsuka, 1985b. Synthesis of (2S,3S)-2,3-octanediol and (S)-2-hydroxy-3-octanone, the male sex pheromone of the grape borer Xylotrechus pyrrhoderus. Tetrahedron, 41: 553–556. |
| Mori, 1985c | Mori, K., T. Uematsu, K. Yanagi and M. Minobe, 1985c. 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 fly pheromone. Tetrahedron, 41: 2751–2758. |
| Mori, 1985d | Mori, K., H. Watanabe, K. Yanagi and M. Minobe, 1985d. 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, 41: 3663–3672. |
| Mori, 1985e | Mori, K. and M. Kato, 1985e. New synthesis of the enantiomers of 14-methyl-1-octadecene, the pheromone of Lyonetia clerkella L. Liebigs Ann. Chem., 2083–2087. |
| Mori, 1985f | Mori, K. and H. Watanabe, 1985f. A new synthesis of serricornin [(4S,6S,7S)-7-hydroxy-4,6-dimethyl-3-nonanone], the sex pheromone of the cigarette beetle. Tetrahedron, 41: 3423–3428. |
| Mori, 1986a | Mori, K. and S. Kuwahara, 1986a. Synthesis of both enantiomers of lardolure, the aggregation pheromone of the acarid mite, Lardoglyphus konoi. Tetrahedron, 42: 5539–5544. |
| Mori, 1986b | Mori, K. and S. Kuwahara, 1986b. Stereochemistry of lardolure. The aggregation pheromone of the acarid mite, Lardoglyphus konoi. Tetrahedron, 42: 5545–5550. |
| Mori, 1986c | Mori, K. and T. Ebata, 1986c. Synthesis of all of the four possible stereoisomers of 5-hydroxy-4-methyl-3-heptanone (sitophilure), the aggregation pheromone of the rice weevil and the maize weevil. Tetrahedron, 42: 4421–4426. |
| Mori, 1986d | Mori, K. and Y. Nakazono, 1986d. Synthesis of both the enantiomers of invictolide, a pheromone component of the red imported fire ant. Tetrahedron, 42: 6459–6464. |
| Mori, 1986e | Mori, K. and T. Ebata, 1986e. Synthesis of (2S, 3R, 1'S, 2'S)-stegobiol, a new component of the drugstore beetle pheromone. Tetrahedron, 42: 4685–4689. |
| Mori, 1986f | Mori, K. and Kisida, H. 1986f. Synthesis of both enantiomers of the heterocyclic pheromones isolated from the male swift moth Hepialus hecta L. Tetrahedron, 42: 5281–5290. |
| Mori, 1986g | Mori, K. and H. Watanabe, 1986g. Enhancement of optical purity of a product by removing unwanted diastereomers in the course of a chiral synthesis: new synthesis of the stereoisomers of 2,8-dimethyl-1,7-dioxaspiro[5,5]undecane, the pheromone of Andrena wilkella. Tetrahedron, 42: 295–304. |
| Mori, 1988a | Mori, K. and Y. Igarashi, 1988a. Synthesis of the four stereoisomers of 6, 12-dimethyl-2-pentadecanone, the sex pheromone of Diabrotica balteata LeConte. Liebigs Ann. Chem. , 1988: 717–720. |
| Mori, 1988b | Mori, K. , T. Yoshimura and T. Sugai, 1988b. Synthesis of (4S, 5R)-5-hydroxy-4-methyl-3-heptanone (sitophilure), the aggregation pheromone of Sitophilus oryzae and S. zeamais. Liebigs Ann. Chem. , 1988: 899–902. |
| Mori, 1988c | Mori, K. and P. Puapoomchareon, 1988c. Synthesis of all of the four stereoisomers of tetrahydro-2,2,6-trimethyl-2H-pyran-3-ol, a volatile compound from the elm bark beetle Pteleobius vittatus. Liebigs Ann. Chem., 175–177. |
| Mori, 1989 | Mori, K. and M. Ishikura, 1989. Synthesis of stiphilate, the aggregation pheromone of Sitophilus granarius L. , and its antipode. Liebigs Ann. Chem. , 1989: 1263–1265. |
| Mori, 1990a | Mori, K. , M. Itou and R. Brossut, 1990. Synthesis of (4R*, 5R*, 6S*, 7E, 9E)-4, 6, 8-trimethyl-7, 9-undecadien-5-ol and its isomers to determine the relative stereochemistry of the female specific compound of the woodroach Cryptocercus punctulatus. Liebigs Ann. Chem. , 1990: 1249–1255. |
| Mori, 1990b | Mori, K. and H. Takikawa, 1990b. A new synthesis of the four stereoisomers of 3,11-dimethyl-2-nonacosanone, the female-produced sex pheromone of the German cockroach. Tetrahedron, 46: 4473–4486. |
| Mori, 1991a | Mori, K. and J. Wu, 1991a. Synthesis of the (5S, 9S)-isomers of 5, 9-dimethylheptadecane and 5, 9-dimethyloctadecane, the major and the minor components of the sex pheromone of Leucoptera malifoliella Costa. Liebigs Ann. Chem. , 1991: 439–443. |
| Mori, 1991b | Mori, K. , H. Harada, P. Zagatti, A. Cork and D. R. Hall, 1991b. Synthesis and biological activity of four stereoisomers of 6, 10, 14-trimethyl-2-pentadecanol, the female-produced sex pheromone of rice moth (Corcyra cephalonica). Liebigs Ann. Chem. , 1991: 259–267. |
| Mori, 1992a | Mori, K. , 1992a. Total Synth. Nat. Prod. , 9: 1–521, DOI: 10. 1002/9780470129722. ch1. |
| Mori, 1992b | Mori, K., M. Amaike and J. E. Oliver, 1992b. Synthesis and absolute configuration of the hemiacetal pheromone of the spined citrus bug Biprorutus bibax. Liebigs Ann. Chem., 1185–1190. |
| Mori, 1992c | Mori, K. and K. Ishigami. 1992c. Synthesis of the enantiomers of rhynchophorol [(E)-6-methyl-2-hepten-4-ol], the male-produced aggregation pheromone of the American palm weevil, Rhynchophorus palmarum. Liebigs Ann. Chem., 11: 1195–1198. |
| Mori, 1993a | Mori, K. , H. Kiyota and D. Rochat, 1993a. Synthesis of the stereoisomers of 3-methyl-4-octanol to determine the absolute configuration of the naturally occurring (3S, 4S)-isomer isolated as the male-produced aggregation pheromone of the African palm weevil, Rhynchophorus phoenics. Liebigs Ann. Chem. , 1993: 865–870. |
| Mori, 1993b | Mori, K. , H. Kiyota, C. Malosse and D. Rochat, 1993b. Synthesis of the enantiomers of syn-4-methyl-5-nonanol to determine the absolute configuration of the naturally occurring (4S, 5S) isomer isolated as the male-produced pheromone compound of Rynchophorus vulneratus and Metamasius hemipterus. Liebigs Ann. Chem. , 1993: 1201–1204. |
| Mori, 1993c | Mori, K. and S. Harashima, 1993c. Synthesis of (2E, 4E, 6R, 10S)-4, 6, 10-trimethyl-2, 4-dodecadiene-7-one – the major component of the sex pheromone of the maritime pine scale (Matsucoccus feytaudi) – and its three stereoisomers. Liebigs Ann. Chem. , 1993: 391–401. |
| Mori, 1993d | Mori, K. and S. Harashima, 1993d. Synthesis of (2E, 4E, 6R, 10R)-4, 6, 10, 12- tetramethyl-2, 4-tridecadien-7-one (matsuone) - the primary component of the sex pheromone of three Matsucoccus pine bast scales – and its antipode. Liebigs Ann. Chem. , 1993: 993–1001. |
| Mori, 1993e | Mori, K., M. Amaike and H. Watanabe, 1993e. New synthesis and revision of the absolute configuration of the hemiacetal pheromone of the spined citrus bug Biprorulus bibax. Liebigs Ann. Chem., 1287–1294. |
| Mori, 1994a | Mori, K., T. Furuuchi and H. Kiyota, 1994a. Pheromone synthesis, CLXV. A new synthesis of (3S,7R,8E,10E)-3,7,9-trimethyl-8,10-dodecadien-6-one, the major component of the sex pheromone of the maritime pine scale. Liebigs Ann. Chem., 971–974. |
| Mori, 1994b | Mori, K. and N. Murata, 1994b. Synthesis of all of the eight stereoisomers of methyl 2, 6, 10-trimethyltridecanoate, the male-produced pheromone of the stink bugs, Euschistus heros and E. obscurus. Liebigs Ann. Chem. , 1994: 1153–1160. |
| Mori, 1994c | Mori, K. and M. Amaike, 1994c. Pheromone synthesis. Part 166. Synthesis of (2E,5R,6E,8E)-5,7-dimethyldeca-2,6,8-trien-4-one, the major component of the sex pheromone of the Israeli pine bast scale, and its antipode. J. Chem. Soc., Perkin Trans. I, 2727–2733. |
| Mori, 1994d | Mori, N., Y. Kuwahara, T. Yoshida and R. Nishida, 1994d. Identification of benzaldehyde, phenol and mandelonitrile from Epanerchodus japonicus Carl (Polydesmida: Polydesmidae) as possible defense substances. Appl. Entomol. Zool., 29: 517–522. |
| Mori, 1995a | Mori, K. and N. Murata, 1995a. A new synthesis of faranal [(3S, 4R, 6E, 10Z)-3, 4, 7, 11-tetramethyl-6, 10-tridecadienal], the trail pheromone of the Pharaoh's ant, Monomorium pharaonis. Liebigs Ann. Chem. , 1995: 2089–2092. |
| Mori, 1995b | Mori, K., T. Furuuchi and K. Matsuyama, 1995b. A new synthesis of (2E,4E,6R,10R)-4,6,10,12-tetramethyl-2,4-tridecadien-7-one (matsuone), the primary component of the sex pheromone of three Matsucoccus pine bast scales. Liebigs Ann. Chem., 2093–2099. |
| Mori, 1995c | Mori, N., Y. Kuwahara, T. Yoshida and R. Nishida, 1995c. Major defensive cyanogen from Parafontaria laminata armigera Verhoeff (Xystodesmidae: Polydesmida). Appl. Entomol. Zool., 30: 197–202. |
| Mori, 1995d | Mori, N., Y. Kuwahara, K. Kurosa, R. Nishida and T. Fukushima, 1995d. Chemical ecology of astigmatid mites XLI. Undecane: the sex pheromone of the acarid mite Caloglyphus rodriguezi Samsinak (Acarina: Acaridae). Appl. Entomol. Zool., 30: 415–423. |
| Mori, 1996a | Mori, K. and H. Horikiri, 1996a. Synthesis of (5R, 11S)-5, 11-dimethylheptadecane and (S)-2, 5-dimethylheptadecane, the major and the minor components of the sex pheromone of the Geometrid moth, Lambdina fiscellaria lugubrosa. Liebigs Ann. Chem. , 1996: 501–505. |
| Mori, 1996b | Mori, K. , T. Nakayama and H. Takikawa, 1996b. Synthesis and absolute configuration of sordidin, the male-produced aggregation pheromone of the banana weevil, Cosmopolites sordidus. Tetrahedron Lett. , 37: 3741–3744. |
| Mori, 1996c | Mori, N., Y. Kuwahara and K. Kurosa, 1996c. Chemical ecology of astigmatid mites XLV. (2R,3R)-Epoxyneral: sex pheromone of the acarid mite Caloglyphus sp. (Acarina: Acaridae). Bioorg. Med. Chem., 4: 289–295. |
| Mori, 1998 | Mori, N., Y. Kuwahara and K. Kurosa, 1998. Rosefuran: the sex pheromone of an acarid mite, Caloglyphus sp. J. Chem. Ecol., 24: 1771–1779. |
| Mori, 2000a | Mori, K. and Y. Takagi, 2000. Enantioselective synthesis of polyzonimine and nitropolyzonamine, spirocyclic compounds from the defensive glands of a millipede, Polyzonium rosalbum. Tetrahedron Lett., 41: 6623–6625. |
| Mori, 2000b | Mori, K., T. Tashiro and S. Sano, 2000b. Enantioselective synthesis of (1S,3S,7R)-3-methyl-α-himachalene, the sex pheromone of the sandfly Lutzomyia longipalpis from Jacobina, Brazil. Tetrahedron Lett., 41: 5243–5247. |
| Mori, 2004a | Mori, K. , T. Ohtaki, H. Ohrui, D. R. Berkebile and D. A. Carlson, 2004a. Synthesis of the four stereoisomers of 6-acetoxy-19-methylnonacosane, the most potent component of the female sex pheromone of the new world screwworm fly, with special emphasis on partial racemization in the course of catalytic hydrogenation. Eur. J. Org. Chem., 1089–1096. |
| Mori, 2004b | Mori, K. , T. Ohtaki, H. Ohrui, D. R. Berkebile and D. A. Carlson, 2004b. Synthesis of the four stereoisomers of 7-acetoxy-15-methylnonacosane, a component of the female sex pheromone of the screwworm fly, Cochliomyia hominivorax. Biosci. Biotechnol. Biochem. , 68: 1768–1778. |
| Mori, 2005 | Mori, K., 2005. Synthesis of (R)-ar-turmerone and its conversion to (R)-ar-himachalene, a pheromone component of the flea beetle: (R)-ar-himachalene is dextrorotatory in hexane, while levorotatory in chloroform. Tetrahedron: Asymmetry, 16: 685–692. |
| Mori, 2006 | Mori, K., 2006. Synthesis of (1S,4R)-4-isopropyl-1-methyl-2-cyclohexen-1-ol, the aggregation pheromone of the ambrosia beetle Platypus quercivorus, its racemate, (1R,4R)- and (1S,4S)-isomers. Tetrahedron: Asymmetry, 17: 2133–2142. |
| Mori, 2007 | Mori, K., 2007. Absolute configuration of gomadalactones A, B and C, the components of the contact sex pheromone of Anoplophora malasiaca. Tetrahedron Lett., 48: 5609–5611. |
| Mori, 2008a | Mori, K., 2008a. Synthesis of the (5S, 9R)-isomer of 5, 9-dimethylpentadecane, the major component of the female sex pheromone of the coffee leaf miner moth, Leucoptera coffeella. Tetrahedron: Asymmetry, 19: 857–861. |
| Mori, 2008b | Mori, K., 2008b. Synthesis of all the six components of the female-produced contact sex pheromone of the German cockroach, Blattella germanica (L. ). Tetrahedron, 64: 4060–4071. |
| Mori, 2008c | Mori, K., T. Tashiro, T. Yoshimura, M. Takita, J. Tabata, S. Hiradate and H. Sugie, 2008c. Determination of the absolute configuration of the male aggregation pheromone, 2-methyl-6-(4'-methylenebicyclo[3.1.0]hexyl)hept-2-en-1-ol, of the stink bug Eysarcoris lewisi (Distant) as 2Z,6R,1'S,5'S by its synthesis. Tetrahedron Lett., 49: 354–357. |
| Mori, 2009a | Mori, K. , 2009a. Synthesis of. all the stereoisomers of 6-methyl-2-octadecanone, 6, 14-diemthyl-2-octadecanone, and 14-methyl2-octadecanone, the components of the female-produced sex pheromone of a moth, Lyclene dharma dharma. Tetrahedron, 65: 2798–2805. |
| Mori, 2009b | Mori, K. and T. Tashiro, 2009b. Synthesis of all the four stereoisomers of (1'S)-1-ethyl-2-methylpropyl 3, 13-dimethylpentadecanoate, the major component of the sex pheromone of Paulownia bagworm, Clania variegate. Tetrahedron Lett. , 50: 3266–3269. |
| Mori, 2010a | Mori, K. , T. Tashiro, B. Zhao, D. M. Suckling and A. M. El-Sayed, 2010. 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 variegate, and its stereoisomer. Tetrahedron, 66: 2642–2653. |
| Mori, 2010b | Mori, K., Y. Shikichi, S. Shankar and J. Y. Yew, 2010b. 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, 66:7161–7168. |
| Mori, 2010c | Mori, K., 2010c. New syntheses of 1,7-dimethylnonyl propanoate, the western corn rootworm pheromone, in four different ways via cross metathesis, alkylation and coupling reactions. Biosci. Biotechnol. Biochem., 74: 595–600. |
| Mori, 2011 | Mori, K., 2011. Pheromone synthesis. Part 247: new synthesis of the enantiomers of 13-methylheptacosane, the female sex pheromone of pear psylla, Cacopsylla pyricola. Tetrahedron: Asymmetry, 22: 1006–1010. |
| Mori, 2012 | Mori, K., 2012. Syntheses of methyl (R,E)-2,4,5-tetradecatrienoate and methyl (2E,4Z)-2,4-decadienoate, the pheromone components of the male dried bean beetle, Acanthoscelides obtectus (Say). Tetrahedron, 68: 1936–1946. |
| Mori, 2015a | Mori, K. and K. Akasaka, 2015a. Pheromone synthesis. Part 256: Synthesis of the four stereoisomers of 5,11-dimethylpentacosane, a new sex pheromone component of the male Galleria mellonella (L.), with high stereochemical purities as determined by the derivatization-HPLC analysis of the eight stereoisomers of 5,11-dimethyl-8-pentacosanol. Tetrahedron, 71: 4102–4115. |
| Mori, 2015b | Mori, K., 2015b. Pheromone synthesis. Part 257: Synthesis of methyl (2E,4Z,7Z)-2,4,7-decatrienoate and methyl (E)-2,4,5-tetradecatrienoate, the pheromone components of the male dried bean beetle, Acanthoscelides obtectus (Say). Tetrahedron, 71: 5589–5596. |
| Mori, 2016a | Mori, K. and C. Y. Yang, 2016a. Pheromone synthesis. Part 259: Synthesis of seven methyl-branched hydrocarbons as the pheromone candidates for female Korean apricot wasp, Eurytoma maslovskiiq. Tetrahedron, 72: 4593-4603. |
| Mori, 2016b | Mori, K. and K. Akasaka, 2016b. Pheromone synthesis. Part 258. Synthesis of the enantiomers of the beetle pheromones ethyl 4-methylheptanoate, 4-methyloctanoic acid and 4-methyl-1-nonanol, and HPLC analysis of their derivatives to determine their enantiomeric purities. Tetrahedron: Asymmetry, 27: 182–187. |
| Mori, 2016c | Mori, K., 2016c. Pheromone synthesis. Part 260: synthesis of (±)-(anti-1,2-dimethyl-3-methylenecyclopentyl) acetaldehyde, the racemate of the female-produced sex pheromone of the pineapple mealybug (Dysmicoccus brevipes), and its syn-isomer. Tetrahedron, 72: 6578–6588. |
| Mori, 2017a | Mori, K. , 2017a. Pheromone synthesis. Part 262: Determination of the absolute configuration of the female sex pheromone [(1S, 2S)-(−)-(1, 2-dimethyl-3-methylenecyclopentyl)acetaldehyde] of the pineapple mealybug (Dysmicoccus brevipes) by synthesis coupled with X-ray analysis. Tetrahedron, 73: 6530–6541. |
| Mori, 2017b | Mori, K. and C. Y. Yang, 2017b. Pheromone synthesis. Part 261: Synthesis of four pyrazines produced by females of the Korean apricot wasp, Eurytoma maslovskii. Tetrahedron, 73: 4766–4769. |
| Mori, 2018 | Mori, K., 2018. Pheromone synthesis. Part 263: synthesis of the racemate and the enantiomers of (E)-cis-6,7-epoxy-2-nonenal, the male-produced pheromone of the red-necked longhorn beetle, Aromia bungii. Tetrahedron, 74: 1444–1448. |
| Mori, 2019 | Mori, K., 2019. Pheromone synthesis. Part 264: Synthesis of the core 3-oxabicyclo[3.3.0]octane structures of gomadalactones A, B and C, the components of the contact sex pheromone of the white-spotted longicorn beetle, Anoplophora malasiaca. Tetrahedron, 75: 3387–3398. |
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