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- Managing the retro-pathway in direct catalytic asymmetric aldol reactions of thioamides. Youmei Bao, Naoya Kumagai, Masakatsu Shibasaki
, Chem. Sci.
, 2015
, 6
, 6124
- Elemental sulfur-promoted one-pot synthesis of 2-(2,2,2-trifluoroethyl)benzoxazoles and their derivatives. Zhengyu Li, Jingnan Dong, Junwen Wang, Ding-Yah Yang, Zhiqiang Weng
, Chem. Commun.
, 2019
, 55
, 13132
- Microplastic emerging pollutants – impact on microbiological diversity, diarrhea, antibiotic resistance, and bioremediation. Karupanagounder Thangaraj Uthra, Vellapandian Chitra, Narayanasamy Damodharan, Anitha Devadoss, Moritz Kuehnel, Antonio Jose Exposito, Sanjay Nagarajan, Sudhagar Pitchaimuthu, Gururaja Perumal Pazhani
, Environ. Sci.: Adv.
, 2023
, 2
, 1469
- Facile access to 3,5-symmetrically disubstituted 1,2,4-thiadiazoles through phosphovanadomolybdic acid catalyzed aerobic oxidative dimerization of primary thioamides. Kazuhisa Yajima, Kazuya Yamaguchi, Noritaka Mizuno
, Chem. Commun.
, 2014
, 50
, 6748
- Access to thiazoline and spiro[indoline-3,3′-thiophene] scaffolds via a formal [3 + 2] annulation reaction of crotonate-derived sulfur ylides and β-ketothioamides. Jing Zheng, Hong Gu, Qinfang Chen, Weiran Yang
, Org. Biomol. Chem.
, 2023
, 21
, 2069
- Second generation of thiazolylmannosides, FimH antagonists for E. coli-induced Crohn's disease. T. Chalopin, D. Alvarez Dorta, A. Sivignon, M. Caudan, T. I. Dumych, R. O. Bilyy, D. Deniaud, N. Barnich, J. Bouckaert, S. G. Gouin
, Org. Biomol. Chem.
, 2016
, 14
, 3913
- One-pot two-component tandem multiple transformations in the synthesis of N,4-diaryl-2,3-dihydropyrrolo[3,4-c]quinolin-1,3-diones and their 3-thioxo-analogues under neat conditions. Sreenivas Avula, Satish Koppireddi, Jayaram Reddy Komsani, Jagadeesh Babu Nanubolu, Rambabu Yadla
, RSC Adv.
, 2013
, 3
, 20990
- Catalytic enantioselective aldol reactions. Yasuhiro Yamashita, Tomohiro Yasukawa, Woo-Jin Yoo, Taku Kitanosono, Shū Kobayashi
, Chem. Soc. Rev.
, 2018
, 47
, 4388
- One-pot method for the synthesis of 1-aryl-2-aminoalkanol derivatives from the corresponding amides or nitriles. Jan Otevrel, David Svestka, Pavel Bobal
, RSC Adv.
, 2020
, 10
, 25029
- Ketoximes to N-substituted thioamides via
PSCl3
mediated Beckmann rearrangement. Uma Pathak, Lokesh Kumar Pandey, Sweta Mathur, M. V. S. Suryanarayana
, Chem. Commun.
, 2009
, 5409