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- Recent advances in the transition metal catalyzed carbonylation of alkynes, arenes and aryl halides using CO surrogates. Prashant Gautam, Bhalchandra M. Bhanage
, Catal. Sci. Technol.
, 2015
, 5
, 4663
- Palladium-catalysed carbonylative α-arylation of nitromethane. Zhong Lian, Stig D. Friis, Troels Skrydstrup
, Chem. Commun.
, 2015
, 51
, 3600
- Carbonylative Suzuki–Miyaura couplings of sterically hindered aryl halides: synthesis of 2-aroylbenzoate derivatives. Aya Ismael, Troels Skrydstrup, Annette Bayer
, Org. Biomol. Chem.
, 2020
, 18
, 1754
- Effect of an aromatic ester conjugate base on E1cB ester hydrolysis. Alkaline hydrolysis of fluorene-9-carboxylate esters. Manoochehr Alborz, Kenneth T. Douglas
, J. Chem. Soc., Perkin Trans. 2
, 1982
, 331
- Pd-Catalysed carbonylative Suzuki–Miyaura cross-couplings using Fe(CO)5 under mild conditions: generation of a highly active, recyclable and scalable ‘Pd–Fe’ nanocatalyst. Zhuangli Zhu, Zhenhua Wang, Yajun Jian, Huaming Sun, Guofang Zhang, Jason M. Lynam, C. Robert McElroy, Thomas J. Burden, Rebecca L. Inight, Ian J. S. Fairlamb, Weiqiang Zhang, Ziwei Gao
, Green Chem.
, 2021
, 23
, 920
- A facile and efficient method for the synthesis of alkynone by carbonylative Sonogashira coupling using CHCl3 as the CO source. Guanglong Sun, Min Lei, Lihong Hu
, RSC Adv.
, 2016
, 6
, 28442
- Synthesis of α,β-alkynyl ketones via the nickel catalysed carbonylative Sonogashira reaction using oxalic acid as a sustainable C1 source. Shaifali, Shankar Ram, Vandna Thakur, Pralay Das
, Org. Biomol. Chem.
, 2019
, 17
, 7036
- Carbonylative synthesis of heterocycles involving diverse CO surrogates. Zhengkai Chen, Le-Cheng Wang, Xiao-Feng Wu
, Chem. Commun.
, 2020
, 56
, 6016
- Iron-catalyzed carbonylation of aryl halides with arylborons using stoichiometric chloroform as the carbon monoxide source. Hongyuan Zhao, Hongyan Du, Xiaorong Yuan, Tianjiao Wang, Wei Han
, Green Chem.
, 2016
, 18
, 5782
- Hydroformylation of olefins and reductive carbonylation of aryl halides with syngas formed ex situ from dehydrogenative decarbonylation of hexane-1,6-diol. Stig Holden Christensen, Esben P. K. Olsen, Jascha Rosenbaum, Robert Madsen
, Org. Biomol. Chem.
, 2015
, 13
, 938