Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Yao-Zhong Jiang"'
Publikováno v:
Journal of Materials Science Letters. 16:747-751
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3a9526dfa8fbbe3df71f5eee78746552
https://doi.org/10.1023/a:1018589316233
https://doi.org/10.1023/a:1018589316233
Publikováno v:
Tetrahedron Letters. 37:4537-4540
The Diels-Alder reactions of N-phenylmaleimide and new chiral 2-sulfinylbutadienes, which were prepared from MerCO[(1R, 2S, 3R)-3-mercaptocamphan-2-ol], produced cycloadducts up to 99% d.e. in the presence of LiClO4 at ambient temperature. On the oth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ff3252d457aa3f3c455ad9d13d7a4231
https://doi.org/10.1016/0040-4039(96)00897-0
https://doi.org/10.1016/0040-4039(96)00897-0
Publikováno v:
Tetrahedron: Asymmetry. 7:57-60
The Diels-Alder reaction of cyclopentadiene with a new chiral α-sulfinylacrylate, which was prepared from MerCO[1R, 2S, 3R)-3- mer capto c amphan-2- o l] at −78°C in the presence of ZnCl2 produced an endo-cycloadduct with 99.4% d.e. in 84% yield.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::10a2f1a54eedcdc0b2329bd36e3e58d4
https://doi.org/10.1016/0957-4166(95)00420-3
https://doi.org/10.1016/0957-4166(95)00420-3
Publikováno v:
ChemInform. 27
The Diels-Alder reaction of cyclopentadiene with a new chiral α-sulfinylacrylate, which was prepared from MerCO[1R, 2S, 3R)-3- mer capto c amphan-2- o l] at −78°C in the presence of ZnCl2 produced an endo-cycloadduct with 99.4% d.e. in 84% yield.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e39b429b23fdb2943d3b6fb595265333
https://doi.org/10.1002/chin.199621035
https://doi.org/10.1002/chin.199621035
Autor:
Masakatsu Shibasaki, Shigeki Matsunaga, Naoya Kumagai, Zhuo Tang, Liu-Zhu Gong, Ai-Qiao Mi, Yao-Zhong Jiang, Masahito Watanabe, Kunihiko Murata, Takao Ikariya
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4a6761024da61d3bf3e6bc8c1f802bf7
https://doi.org/10.1002/0470862017.ch11
https://doi.org/10.1002/0470862017.ch11
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
Publikováno v:
Acta Crystallographica Section C Crystal Structure Communications. 51:2085-2087
The crystal structure of N 2 H 5 + .C 4 H 5 O 6 - consists of infinite chains of tartrate anions linked head-to-tail by O-H...O hydrogen bonds. Two such chains are cross-connected by O-H...O hydrogen bonds to form dimeric chains. The hydrazinium cati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7dd34c42eba111a6fcad70b44ac1c269
https://doi.org/10.1107/s0108270195005488
https://doi.org/10.1107/s0108270195005488
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
Autor:
Xiao-Hua Chen, Shi-Wei Luo, Zhuo Tang, Lin-Feng Cun, Ai-Qiao Mi, Yao-Zhong Jiang, Liu-Zhu Gong
Publikováno v:
Chemistry - A European Journal; Jan2007, Vol. 13 Issue 2, p689-701, 13p
Publikováno v:
Journal of Organic Chemistry; 2/4/2005, Vol. 70 Issue 3, p1006-1010, 5p, 5 Charts