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- Facile synthesis of 4- and 7-azaindoles from the corresponding imines by palladium-catalyzed cascade C–C and C–N coupling. Ngo Nghia Pham, Thanh Tuan Dang, Ngoc Thang Ngo, Alexander Villinger, Peter Ehlers, Peter Langer
, Org. Biomol. Chem.
, 2015
, 13
, 6047
- Introducing nitrogen atoms to amidoalkylindoles: potent and selective cannabinoid type 2 receptor agonists with improved aqueous solubility. Yue-Yang Ji, Zhi-Long Wang, Fang-Ning Pei, Jun-Jie Shi, Jiao-Jiao Li, Hendra Gunosewoyo, Fan Yang, Jie Tang, Xin Xie, Li-Fang Yu
, Med. Chem. Commun.
, 2019
, 10
, 2131
- Mild one-pot Horner–Wadsworth–Emmons olefination and intramolecular N-arylation for the syntheses of indoles, all regio-isomeric azaindoles, and thienopyrroles. Ji Hye Choi, Hwan Jung Lim
, Org. Biomol. Chem.
, 2015
, 13
, 5131
- Synthetic strategies for aryl/heterocyclic selenides and tellurides under transition-metal-catalyst free conditions. Debasish Kundu
, RSC Adv.
, 2021
, 11
, 6682
- Fragment optimization and elaboration strategies – the discovery of two lead series of PRMT5/MTA inhibitors from five fragment hits. Christopher R. Smith, Svitlana Kulyk, Misbha Ud Din Ahmad, Valentina Arkhipova, James G. Christensen, Robin J. Gunn, Anthony Ivetac, John M. Ketcham, Jon Kuehler, J. David Lawson, Nicole C. Thomas, Xiaolun Wang, Matthew A. Marx
, RSC Med. Chem.
, 2022
, 13
, 1549
- Transition-metal mediated carbon–sulfur bond activation and transformations: an update. Jiang Lou, Quannan Wang, Ping Wu, Hongmei Wang, Yong-Gui Zhou, Zhengkun Yu
, Chem. Soc. Rev.
, 2020
, 49
, 4307
- Visible-light-induced synthesis of N-disulfanyl indoles, pyrroles or carbazoles via the construction of stable S–S–N bonds. Tianfeng Lao, Jianxin Chen, Xianhang Zhou, Ziwu Zhang, Gao Cao, Zhengquan Su, Yue Yu, Hua Cao
, Chem. Commun.
, 2023
, 59
, 458
- Coexistence of an antiferromagnetically coupled dimer and isolated paramagnetic spin in 4-azaindol-2-yl nitronyl nitroxide crystal. Hideaki Nagashima, Noriko Hashimoto, Hidenari Inoue, Naoki Yoshioka
, New J. Chem.
, 2003
, 27
, 805
- Synthesis and biological evaluation of 2,3-bis(het)aryl-4-azaindole derivatives as protein kinase inhibitors. Frédéric Pin, Frédéric Buron, Fabienne Saab, Lionel Colliandre, Stéphane Bourg, Françoise Schoentgen, Remy Le Guevel, Christiane Guillouzo, Sylvain Routier
, Med. Chem. Commun.
, 2011
, 2
, 899
- Recent developments in the synthesis of azaindoles from pyridine and pyrrole building blocks. Damoder Reddy Motati, Radhika Amaradhi, Thota Ganesh
, Org. Chem. Front.
, 2021
, 8
, 466