Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Min Sup Park"'
Publikováno v:
Polymer Korea. 44:132-138
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9575d70fdba653747cdab00bd4f799da
https://doi.org/10.7317/pk.2020.44.2.132
https://doi.org/10.7317/pk.2020.44.2.132
Autor:
Kim，Young Wun, Jeongkwon Kim, Jae Hee Song, Jisoo Hong, Joon Ho Kim, Kim， Yeong Joon, Min Sup Park
Publikováno v:
Polymer Korea. 43:394-400
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::09344a38b7cb8fc89aa842c931f2abcb
https://doi.org/10.7317/pk.2019.43.3.394
https://doi.org/10.7317/pk.2019.43.3.394
Publikováno v:
Bulletin of the Korean Chemical Society. 23:1830-1832
Bio-Organic Science Division, Korea Research Institute of Chemical Technology, P.O. Box 107, Yusong, Daejon 305-600, KoreaReceived June 24, 2002Key Words : Ruthenium tetroxide, Quinoline, Isoquinoline, Pyridinedicarboxylic acidThe chloropyridine moie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f93ee9d897da0df7b399fce34bb1ac33
https://doi.org/10.5012/bkcs.2002.23.12.1830
https://doi.org/10.5012/bkcs.2002.23.12.1830
Publikováno v:
ChemInform. 30
Acid-catalyzed benzidine rearrangements of new unsymmetrical diazanes 1-3, prepared from the reduction of corresponding diazenes 4-6, were carried out in ethanolic solutions. The results are as follows; rearrangement of (3-carbomethoxyphenyl)(3-metho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::68546f02699609fc802fe7d4c69574f7
https://doi.org/10.1002/chin.199910047
https://doi.org/10.1002/chin.199910047
Publikováno v:
ChemInform. 35
The nucleophilic aromatic substitution on 5‐chloropyrazoles activated by the electron‐withdrawing formyl group offers a useful method to introduce a wide range of N‐containing heterocycles into them. The rate of reaction was greatly affected by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4ff40bebafa989db5ef034a0928d9dc2
https://doi.org/10.1002/chin.200439108
https://doi.org/10.1002/chin.200439108