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- Design, synthesis, and structure–activity relationships of 1,3,4-oxadiazol-2(3H)-ones as novel FAAH inhibitors. László E. Kiss, Humberto S. Ferreira, Alexandre Beliaev, Leonel Torrão, Maria João Bonifácio, David A. Learmonth
, Med. Chem. Commun.
, 2011
, 2
, 889
- Recent advances in chemistry and therapeutic potential of functionalized quinoline motifs – a review. Olayinka O. Ajani, King T. Iyaye, Olabisi T. Ademosun
, RSC Adv.
, 2022
, 12
, 18594
- Palladium-catalyzed direct ortho-ethoxycarbonylation of azobenzenes and azoxybenzenes with diethyl azodicarboxylate. Ning Xu, Dengke Li, Yicheng Zhang, Lei Wang
, Org. Biomol. Chem.
, 2015
, 13
, 9083
- Metal-free, efficient hydrazination of imidazo[1,2-a]pyridine with diethyl azodicarboxylate in neutral media. Yuanxiang Wang, Brendan Frett, Nick McConnell, Hong-yu Li
, Org. Biomol. Chem.
, 2015
, 13
, 2958
- Highly stereoselective synthesis of cis-β-enaminones mediated by diethyl azodicarboxylate. Xiaoliang Xu, Ping Du, Dongping Cheng, Hong Wang, Xiaonian Li
, Chem. Commun.
, 2012
, 48
, 1811
- Versatile and highly efficient oxidative C(sp3)–H bond functionalization of tetrahydroisoquinoline promoted by bifunctional diethyl azodicarboxylate (DEAD): scope and mechanistic insights. Takuya Suga, Sunao Iizuka, Takahiko Akiyama
, Org. Chem. Front.
, 2016
, 3
, 1259
- Palladium-catalyzed direct C–H ethoxycarbonylation of 2-aryl-1,2,3-triazoles and efficient synthesis of suvorexant. Rui Sang, Yang Zheng, Hailong Zhang, Xiaohua Wu, Qiantao Wang, Li Hai, Yong Wu
, Org. Chem. Front.
, 2018
, 5
, 648
- Advances and mechanistic insight on the catalytic Mitsunobu reaction using recyclable azo reagents. Daisuke Hirose, Martin Gazvoda, Janez Košmrlj, Tsuyoshi Taniguchi
, Chem. Sci.
, 2016
, 7
, 5148
- Glycosylation with ulosonates under Mitsunobu conditions: scope and limitations. Nándor Kánya, Sándor Kun, Gyula Batta, László Somsák
, New J. Chem.
, 2020
, 44
, 14463
- Study of short-lived and early reaction intermediates in organocatalytic asymmetric amination reactions by ion-mobility mass spectrometry. Jun-Ting Zhang, Hao-Yang Wang, Xiang Zhang, Fang Zhang, Yin-Long Guo
, Catal. Sci. Technol.
, 2016
, 6
, 6637