Zobrazeno 1 - 10
of 126
pro vyhledávání: '"Zhang-Pei Chen"'
Autor:
Chen-Chen Li, Haining Wang, Malcolm M. Sim, Zihang Qiu, Zhang-Pei Chen, Rustam Z. Khaliullin, Chao-Jun Li
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-9 (2020)
Alcohols are more naturally abundant than carbonyl compounds, which in turn are well known for their reactivity in Grignard reactions. Here, the authors showcase a distinct Grignard-like reactivity by using alcohols as coupling partners with hydrazon
Externí odkaz:
https://doaj.org/article/c45718de9c8b46ddba7d11418ba37090
Autor:
Zhou, Yang-Yang, Du, Xiao-Jing, Zhang, Chi-Hao, Aparicio, Thomas, Zaanan, Aziz, Afchain, Pauline, Chen, Li-Ping, Hu, Sun-Kuan, Zhang, Pei-Chen, Wu, Ming, Zhang, Qing-Wei, Wang, Hong
Publikováno v:
In EBioMedicine March 2019 41:276-285
Autor:
Tuan-Yu Guo, Zhang-Pei Chen, Jiao-Fen Lin, Zhen-Zhen Cai, Hong-Lu Xie, Aikebaier Reheman, Ying-Gang Jia
Publikováno v:
Journal of Molecular Structure. 1283:135282
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3dc097b5733762c2b965433bbe0f2ab8
https://doi.org/10.1016/j.molstruc.2023.135282
https://doi.org/10.1016/j.molstruc.2023.135282
Publikováno v:
Nanomaterials, Vol 7, Iss 7, p 169 (2017)
The morphological control of polymer micellar aggregates is an important issue in applications such as nanomedicine and material science. Stimuli responsive soft materials have attracted significant attention for their well-controlled morphologies. H
Externí odkaz:
https://doaj.org/article/30554284baf44baab98a4eca190b4197
Autor:
Han, Shao-Liang, Zhou, Hong-Zhong, Cheng, Jun, Lan, Sheng-Hong, Zhang, Pei-Chen, Chen, Zhe-Jing, Zeng, Qi-Qiang
Publikováno v:
In Asian Journal of Surgery 2009 32(1):1-6
Publikováno v:
Advanced Synthesis & Catalysis. 359:2762-2767
An enantioselective iridium-catalyzed direct hydrogenation of heteroaromatics containing two nitrogen atoms, 3-substituted pyrrolo[1,2-a]pyrazines, has been successfully achieved, providing a facile synthesis of optically active 1,2,3,4-tetrahydropyr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f1a0650bc8e31cddf4e465e14ca6b4fa
https://doi.org/10.1002/adsc.201700431
https://doi.org/10.1002/adsc.201700431
Publikováno v:
Organic Letters. 18:4650-4653
A highly enantioselective synthesis of chiral fluorinated propargylamines was developed through phosphoric acid and ruthenium-catalyzed chemoselective biomimetic hydrogenation of the carbon-nitrogen double bond of fluorinated alkynyl ketimines in the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b2aa2dc9c8408c283573135ff214ff5
https://doi.org/10.1021/acs.orglett.6b02283
https://doi.org/10.1021/acs.orglett.6b02283
Publikováno v:
Organic Letters. 18:2676-2679
An enantioselective hydrogenation of fluorinated hydrazones has been achieved by employing [Pd(R)-DTBM-SegPhos(OCOCF3)2] as the catalyst, providing a general and convenient method toward chiral fluorinated hydrazines. A broad substrate scope includin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8543f67a04bd87766d1c60d08f2e04f8
https://doi.org/10.1021/acs.orglett.6b01118
https://doi.org/10.1021/acs.orglett.6b01118
Autor:
Zhang-Pei Chen, Yong-Gui Zhou
Publikováno v:
Synthesis. 48:1769-1781
Enantiopure heterocyclic architectures containing two or more heteroatoms in the ring system have attracted considerable attraction due to this motif playing a role of great importance in asymmetric synthesis and the pharmaceutical chemistry. This re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::47506d85e72522af2ff00fe0900032f4
https://doi.org/10.1055/s-0035-1561622
https://doi.org/10.1055/s-0035-1561622
Publikováno v:
ACS Catalysis. 5:6086-6089
An efficient approach toward the synthesis of cyclic and linear chiral trifluoromethyl substituted hydrazines was developed by Pd-catalyzed asymmetric hydrogenation of both N-acyl and N-aryl hydrazones in excellent yields and up to 97% ee. A successf
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2311d66b51c4b6c30b666371e4939a2e
https://doi.org/10.1021/acscatal.5b01641
https://doi.org/10.1021/acscatal.5b01641