Computational insight into the mechanism of the Pd(0)–Brønsted acid cooperatively catalysed head-to-tail dimerization of terminal alkynes

RSC Advances ◽  
2015 ◽  
Vol 5 (103) ◽  
pp. 84636-84642 ◽  
Author(s):  
Hao Zhang ◽  
Xiaoguang Bao

The Pd(0)–Brønsted acid cooperatively catalysed head-to-tail dimerization of terminal alkynes was computationally studied to gain a mechanistic insight.

ChemCatChem ◽  
2018 ◽  
Vol 10 (11) ◽  
pp. 2442-2449 ◽  
Author(s):  
Pietro Giacinto ◽  
Andrea Bottoni ◽  
Andrea Garelli ◽  
Gian Pietro Miscione ◽  
Marco Bandini

2020 ◽  
Vol 16 ◽  
pp. 88-105
Author(s):  
Katarzyna Włodarczyk ◽  
Piotr Borowski ◽  
Marek Stankevič

β-Hydroxyalkylphosphine sulfides undergo [1,3]- or [1,4]-sulfur atom phosphorus-to-carbon migration in the presence of Lewis or Brønsted acids. The direction of sulfur atom migration depends on the type of acid used for the reaction. In the presence of a Brønsted acid, mainly [1,3]-rearrangement is observed, whereas a Lewis acid catalyzes the [1,4]-sulfur migration. To gain insight into the mechanism of these transformations, the stereochemistry of these rearrangements have been tested, along with the conduction of some control experiments and DFT calculations.


2014 ◽  
Vol 1 (10) ◽  
pp. 1197-1200 ◽  
Author(s):  
Qingjiang Li ◽  
Xiao-Shui Peng ◽  
Henry N. C. Wong

A simple and efficient approach for the synthesis of disubstituted carbazoles has been developed from o-haloanilines and terminal alkynes using a two-step strategy, namely, Sonogashira coupling and intramolecular cyclization.


2017 ◽  
Vol 54 (1) ◽  
pp. 54-63 ◽  
Author(s):  
Xu Li ◽  
Lan Wu ◽  
Qiong Tang ◽  
Jinxiang Dong

Author(s):  
Mizzanoor Rahaman ◽  
M. Shahnawaz Ali ◽  
Khorshada Jahan ◽  
Damon Hinz ◽  
Jawad Bin Belayet ◽  
...  

2021 ◽  
Author(s):  
Sergio Rojas-Buzo ◽  
Benjamin Bohigues ◽  
Christian W. Lopes ◽  
Débora M. Meira ◽  
Mercedes Boronat ◽  
...  

The Brønsted/Lewis acid properties of Hf-MOF-808 can be tuned by simply controlling the solvent employed in its synthesis, with direct catalytic implications on the activity and selectivity of organic reactions sensitive to the active site nature.


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