Impact of Viewing vs. Not Viewing a Real Forest on Physiological and Psychological Responses in the Same Setting

Autor: Haruo Saito, Norio Nishiyama, Junko Endo, Norimasa Takayama, Akio Fujiwara, Kazutaka Murase, Masahiro Horiuchi

Publikováno v: International Journal of Environmental Research and Public Health, Vol 11, Iss 10, Pp 10883-10901 (2014)
International Journal of Environmental Research and Public Health
Volume 11
Issue 10
Pages 10883-10901

We investigated the impact of viewing versus not viewing a real forest on human subjects’ physiological and psychological responses in the same setting. Fifteen healthy volunteers (11 males, four females, mean age 36 years) participated. Each parti

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::255494a9aa35b4d323501cc9fe3c8264
http://www.mdpi.com/1660-4601/11/10/10883

Diastereoface-differentiating oxidation of 1-cyclohexenyl ether using a 2,4-pentanediol tether

Autor: Norio Nishiyama, Takashi Sugimura, Akira Tai, Rumiko Tsuchida, Hiromitsu Iguchi, Tadao Hakushi

Publikováno v: Tetrahedron: Asymmetry. 9:1007-1013

Diastereoface-differentiating oxidation of the chiral enol ether prepared from cyclohexanone and optically active 2,4-pentanediol gave a diastereomeric mixture of the corresponding 2-hydroxycyclohexanone acetal. The diastereomeric excess of the produ

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::db645cacbd7e04265c56538f8e3c3369
https://doi.org/10.1016/s0957-4166(98)00046-9

Regio- and diastereo-chemically controlled photocycloaddition of an arene and an alkene linked by a chiral auxiliary

Autor: Akira Tai, Tadao Hakushi, Norio Nishiyama, Takashi Sugimura

Publikováno v: Tetrahedron: Asymmetry. 5:1163-1166

Intramolecular meta -arene-alkene photocycloaddition of 1b , the substrate having a chiral auxiliary as a linking bridge between the arene and the alkene, resulted in high diastereofacial differentiation of the alkene at the addition step and suffici

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::305c0316d15bd059fa3417b958f83df9
https://doi.org/10.1016/0957-4166(94)80147-9

ChemInform Abstract: Enantiospecific Preparation of gem-Dimethylcyclopropane Fused Cycloheptanes via Valence Tautomerization of 3,4-Homotropilidene under Thermodynamic and Kinetic Control

Autor: Norio Nishiyama, Akira Tai, Toshifumi Katagiri, Takashi Sugimura, Tohru Futagawa

Publikováno v: ChemInform. 28

3,4-Homotropilidene derivatives were obtained as a stable compound by regioselective dichlorocarbene addition to 4-alkoxy-8,8-dimethylcycloheptatrienes. Substitution of chlorine atomes to hydrogens in them by reduction with sodium affords rearranged

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::6f77a76652a4d563a0c4c72fb6886843
https://doi.org/10.1002/chin.199702078

Diastereoface differentiating peracid oxidation of the enol ether derived from cyclohexanone and 2,4-pentanediol: Preparation of optically pure 2-hydroxycyclohexanone acetal

Autor: Norio Nishiyama, Tadao Hakushi, Takashi Sugimura, Akira Tai

Publikováno v: Tetrahedron: Asymmetry. 4:43-44

Diastereoface differentiating m-chloroperbenzoic acid oxidation of the chiral enol ether prepared from cyclohexanone and optically active 2,4-pentanediol proceeded from −72 to 39 °C to give a diastereomeric mixture of the corresponding 2-hydroxycy

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::06467819a4a9ed4825530631df5be0d6
https://doi.org/10.1016/s0957-4166(00)86013-9