Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Xudong Geng"'
Autor:
Xudong Geng, Xuancheng Du, Weijie Wang, Chengmei Zhang, Xiangdong Liu, Yuanyuan Qu, Mingwen Zhao, Weifeng Li, Mingzhen Zhang, Kangsheng Tu, Yong-Qiang Li
Publikováno v:
ACS Nano. 17:7443-7455
Autor:
Jianlong Jin, Xudong Geng, Qunxing Huang, Ya Yuan, Jian Dong, Chengqian Lin, Bo Li, Luwei Yang
Publikováno v:
Drying Technology. :1-15
Publikováno v:
International Journal of Hydrogen Energy.
Publikováno v:
Applied Thermal Engineering. 218:119377
Publikováno v:
Energy. 239:122651
To achieve efficient and reliable heating in severe cold regions below −20 °C, this paper investigates a R134a/CO2 cascade air source heat pump system (ASHP). Firstly, a simulation model is constructed and used for energy performance analysis. The
Autor:
Ilaria Zanardi, Jon Mallen-St. Clair, Iwao Ojima, Susan Band Horwitz, Shujun Xia, Xianrui Zhao, Dafna Bar-Sagi, David Gallager, Jin Chen, Tao Wang, Xudong Geng, Michael L. Miller, Ralph J. Bernacki, Larisa V. Kuznetsova, Songnian Lin, Jean M. Veith, Jennifer L. Guerriero, Chuanxing Qu, Liang Sun, Christopher P. Borella, Paula Pera
Publikováno v:
Journal of Medicinal Chemistry. 51:3203-3221
Novel second-generation taxoids with systematic modifications at the C2, C10, and C3'N positions were synthesized and their structure-activity relationships studied. A number of these taxoids exhibited exceptionally high potency against multidrug-res
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 14:3491-3494
Based on a common pharmacophore model and the hypothesis that the baccatin core of taxoids is a scaffold securing the proper orientation of the side chains, a bicyclic alkaloid scaffold was designed as a baccatin surrogate. Using this scaffold, two n
Publikováno v:
Angewandte Chemie. 116:2616-2619
Publikováno v:
Angewandte Chemie. 116:2611-2615
Autor:
Xudong Geng, Samuel J. Danishefsky
Publikováno v:
Organic Letters. 6:413-416
[reaction: see text] The first total synthesis of resorcinylic macrolide aigialomycin D was described. The resorcinylic moiety was constructed by a highly efficient Diels-Alder reaction using a disiloxydiene and a 14-membered "ynolide" as the dienoph