Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Liangyou He"'
Autor:
Hiroshi Sakamaki, T. Tomoyoshi Takahashi, C. Akira Horiuchi, Yoshikazu Saitoh, Masatoshi Matsushita, Kenji Funayama, Ken-ichi Itoh, Chikao Hashimoto, Miyuki Kanamori, Takashi Sugiyama, Liangyou He, Takamitsu Utsukihara
Publikováno v:
Applied Organometallic Chemistry. 21:1029-1032
The reaction of α,β-unsaturated ketones with cerium (IV) sulfate tetrahydrate [Ce(SO4)2·4H2O, CS] in acetic acid gave the corresponding β-acetoxy ketones. In the case of 2-cyclohexen-1-one with CS in acetic acid, benzobicyclo[2.2.2]octen-2-one wa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0747621aeb11bf37c1b91b4b78358091
https://doi.org/10.1002/aoc.1326
https://doi.org/10.1002/aoc.1326
Autor:
Liangyou He, Shigeo Takahashi, Sukekatsu Nozaki, C. Akira Horiuchi, Masatoshi Matsushita, Takamitsu Utsukihara, Takashi Sugiyama, Chikao Hashimoto, Yoshikazu Saitoh, T. Tomoyoshi Takahashi
Publikováno v:
Applied Organometallic Chemistry. 20:663-668
Reaction of α,β-unsaturated ketones with cerium(IV) salts or lanthanide triflates in alcohols gave good yields of the corresponding β-alkoxy compounds. In the case of 2-cyclopentenone and 2-cyclohexenone, the 1,1,3-trialkoxy acetal derivatives wer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eafde6d3eb0f8db848bc385753dfc2eb
https://doi.org/10.1002/aoc.1096
https://doi.org/10.1002/aoc.1096
Autor:
C. Akira Horiuchi, Liangyou He
Publikováno v:
Bulletin of the Chemical Society of Japan. 72:2515-2521
The reaction of 2-substituted cycloalkanones with cerium(IV) sulfate tetrahydrate (CS) in alcohols and acetic acid gave the corresponding alkyl esters of oxo acids (80—96%) and oxo acids (78—96%), respectively, by oxidative cleavage of the C(R)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0c27261033e6db32746fccf17cc4a26e
https://doi.org/10.1246/bcsj.72.2515
https://doi.org/10.1246/bcsj.72.2515
Publikováno v:
ChemInform. 30
The reaction of 2-alkylcycloalkanones with iodine–cerium(IV) salts in alcohols (methanol, ethanol, propan-1-ol or propan-2-ol) gave the respective oxo ester in 28–98% yields.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3377e6134b0140da350ab814e8326135
https://doi.org/10.1002/chin.199931096
https://doi.org/10.1002/chin.199931096
Autor:
Liangyou He, C. Akira Horiuchi
Publikováno v:
ChemInform. 31
The reaction of 2-substituted cycloalkanones with cerium(IV) sulfate tetrahydrate (CS) in alcohols and acetic acid gave the corresponding alkyl esters of oxo acids (80—96%) and oxo acids (78—96%), respectively, by oxidative cleavage of the C(R)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0e9a428521404ed3dc4778ff0cad9b73
https://doi.org/10.1002/chin.200006076
https://doi.org/10.1002/chin.200006076
Autor:
Liangyou He, C. Akira Horiuchi
Publikováno v:
Applied Organometallic Chemistry. 13:867-869
A new method for the direct conversion of oximes into aldehydes and ketones by treatment with cerium(IV) salts is described. Cerium(IV) salts can be used as an effective and mild oxidizing agent for the regeneration of carbonyl compounds from oximes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c32ead5b3bfe7f0ac78cd53f6ef8a46b
https://doi.org/10.1002/(sici)1099-0739(199912)13:12<867::aid-aoc928>3.0.co
https://doi.org/10.1002/(sici)1099-0739(199912)13:12<867::aid-aoc928>3.0.co
Autor:
C. Akira Horiuchi, Liangyou He
Publikováno v:
ChemInform. 31
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1bef962b15c854efbdd59fbf23c5a6f0
https://doi.org/10.1002/chin.200040035
https://doi.org/10.1002/chin.200040035
Autor:
C. Akira Horiuchi, Liangyou He
Publikováno v:
Journal of Chemical Research. 2000:172-173
The reaction of 1-phenylcycloalkenes and derivatives of styrene with cerium(IV) sulfate tetrahydrate in methanol leads to the formation of 1,2-dimethoxy compounds (54–89%).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::28c98188f70ebdb852358447097a074d
https://doi.org/10.3184/030823400103167039
https://doi.org/10.3184/030823400103167039
Publikováno v:
Journal of Chemical Research. 23:122-123
The reaction of 2-alkylcycloalkanones with iodine–cerium(IV) salts in alcohols (methanol, ethanol, propan-1-ol or propan-2-ol) gave the respective oxo ester in 28–98% yields.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f5bb3f84edac9efcf017c2c1b379398
https://doi.org/10.1177/174751989902300228
https://doi.org/10.1177/174751989902300228