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- Gold(i)-catalyzed addition of carboxylic acids to internal alkynes in aqueous medium. Pedro J. González-Liste, Sergio E. García-Garrido, Victorio Cadierno
, Org. Biomol. Chem.
, 2017
, 15
, 1670
- Electro-organic synthesis: an environmentally benign alternative for heterocycle synthesis. Suman Devi, Jyoti, Kiran, Deepak Wadhwa, Jayant Sindhu
, Org. Biomol. Chem.
, 2022
, 20
, 5163
- An investigation of 1,4,7-tri(4-alkynyl)-1,4,7-triazacyclononanes: ligand synthesis and metal co-ordination chemistry . Murray V. Baker, David H. Brown, Brian W. Skelton, Allan H. White
, J. Chem. Soc., Dalton Trans.
, 2000
, 4607
- Alkyne insertion into Cu–Al bonds and selective functionalization to form copper acyl compounds. Caitilín McManus, Agamemnon E. Crumpton, Simon Aldridge
, Chem. Commun.
, 2022
, 58
, 8274
- Copper-catalyzed regioselective trans-silaboration of internal arylalkynes with stereochemical switch to cis-addition mode. Toshimichi Ohmura, Yuta Takaoka, Michinori Suginome
, Chem. Commun.
, 2021
, 57
, 4670
- One-pot, two-step conversion of alkynes to α-amino (α,α-diamino) ketones with a DMF-activated N-bromoimide strategy. Mengru Li, Luyan Zhang, Baozhong Zhao, Fushun Liang
, RSC Adv.
, 2016
, 6
, 93325
- Synthesis of indoles from aroyloxycarbamates with alkynes via decarboxylation/cyclization. Nuannuan Ma, Peihe Li, Zheng Wang, Qipu Dai, Changwen Hu
, Org. Biomol. Chem.
, 2018
, 16
, 2421
- Palladium-catalyzed hydroboration reaction of unactivated alkynes with bis (pinacolato) diboron in water. Ming Yang, Yunzi Yu, Wenxia Ma, Yuqin Feng, Gang Zhang, Yaqi Wu, Fanyu Zhou, Yongsheng Yang, Dezheng Liu
, RSC Adv.
, 2022
, 12
, 9815
- Cp*Co(iii)-catalyzed vinylic C–H bond activation under mild conditions: expedient pyrrole synthesis via (3 + 2) annulation of enamides and alkynes. Dhanaji M. Lade, Amit B. Pawar
, Org. Chem. Front.
, 2016
, 3
, 836
- Recent developments in the control of selectivity in hydrogenation reactions by confined metal functionalities. Moussa Zaarour, Jurjen Cazemier, Javier Ruiz-Martínez
, Catal. Sci. Technol.
, 2020
, 10
, 8140