Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Lin-Feng Cun"'
Publikováno v:
Journal of Applied Polymer Science. 65:1883-1887
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0ca6f080260ad82ae7a11e633f9be3ed
https://doi.org/10.1002/(sici)1097-4628(19970906)65:10<1883::aid-app4>3.0.co
https://doi.org/10.1002/(sici)1097-4628(19970906)65:10<1883::aid-app4>3.0.co
Publikováno v:
Journal of Applied Polymer Science. 64:1719-1723
Copolymerizations of 1,3-pentadiene (PD) with 1,3-cyclopentadiene (CPD) initiated by aluminium trichloride were carried out in toluene. The addition of CPD in the PD polymerization system does not affect the molecular weight but greatly increases the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1dfd9c99f52fe23d14013b60b8aa5446
https://doi.org/10.1002/(sici)1097-4628(19970531)64:9<1719::aid-app7>3.0.co
https://doi.org/10.1002/(sici)1097-4628(19970531)64:9<1719::aid-app7>3.0.co
Publikováno v:
Journal of Polymer Science Part A: Polymer Chemistry. 34:3527-3530
endo-Dicyclopentadiene (DCPD) was polymerized by various cationic initiating systems in different solvents. IR and 1H NMR results show that four types of structural units are formed due to the corresponding addition modes: the addition on the norborn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f27169042db9f14a8c63c0ba8f98c43b
https://doi.org/10.1002/(sici)1099-0518(199612)34:17<3527::aid-pola6>3.0.co
https://doi.org/10.1002/(sici)1099-0518(199612)34:17<3527::aid-pola6>3.0.co
Publikováno v:
Polymer. 37:3979-3982
The polymerizations of 2-methyl-2-butene (2M2B) were carried out by various cationic initiators in different media at 30°C. All these polymerizations generate oily oligomers of rather low degrees of polymerization (3–5). Evidences from i.r. and 1H
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::104cbeda8ee2bc18844d56244c8d4b02
https://doi.org/10.1016/0032-3861(96)00200-5
https://doi.org/10.1016/0032-3861(96)00200-5
Publikováno v:
Journal of Polymer Science Part A: Polymer Chemistry. 34:903-906
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::907626358bc529fa3bc6981c4a288954
https://doi.org/10.1002/(sici)1099-0518(19960415)34:5<903::aid-pola19>3.0.co
https://doi.org/10.1002/(sici)1099-0518(19960415)34:5<903::aid-pola19>3.0.co
Publikováno v:
The Journal of organic chemistry. 72(26)
A variety of organocatalysts for the asymmetric direct aldol reactions of ketones with alpha-keto acids were designed on the basis of molecular recognition and prepared from proline and aminopyridines. The organic molecule 8e, derived from proline an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da060734950abc9c4b78a5fd85c7f078
https://pubmed.ncbi.nlm.nih.gov/18004868
https://pubmed.ncbi.nlm.nih.gov/18004868
Publikováno v:
ChemInform. 38
Direct aldol reactions of aldehydes with methylthio- and fluoroacetone catalyzed by proline amides have been investigated. l -Prolinamide 5e was found to be the best catalyst. Under the optimized reaction conditions, a series of aromatic and aliphati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d1352d4a539123c8b8c3aa46fd2e3ea5
https://doi.org/10.1002/chin.200727032
https://doi.org/10.1002/chin.200727032
Autor:
Zhuo, Tang, Zhi-Hua, Yang, Xiao-Hua, Chen, Lin-Feng, Cun, Ai-Qiao, Mi, Yao-Zhong, Jiang, Liu-Zhu, Gong
Publikováno v:
Journal of the American Chemical Society. 127(25)
L-proline amides derived from various chiral beta-amino alcohols that bear substituents with various electron natures at their stereogenic centers are prepared and evaluated for catalyzing the direct Aldol reaction of 4-nitrobenzaldehyde with acetone
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3e5f6ca167204f3465d4314035106488
https://pubmed.ncbi.nlm.nih.gov/15969611
https://pubmed.ncbi.nlm.nih.gov/15969611
Autor:
Quan-Zhong, Liu, Nan-Sheng, Xie, Zhi-Bin, Luo, Xin, Cui, Lin-Feng, Cun, Liu-Zhu, Gong, Ai-Qiao, Mi, Yao-Zhong, Jiang
Publikováno v:
The Journal of organic chemistry. 68(20)
A family of optically pure 7,7'-disubsituted-2,2'-dihydroxy-1,1'-dinaphthyls have been conveniently prepared from easily accessible 7-alloxyl-2-naphthol by reaction sequences beginning with the asymmetric oxidative coupling and followed by key synthe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7fda0722dbe7b7441588d0ed8898f775
https://pubmed.ncbi.nlm.nih.gov/14510582
https://pubmed.ncbi.nlm.nih.gov/14510582
Publikováno v:
Organic Letters; May2011, Vol. 13 Issue 9, p2472-2475, 4p