Efficient synthesis of pyrrolo[1,2-a]quinoxalines catalyzed by a Brønsted acid through cleavage of C–C bonds

2016 ◽  
Vol 14 (36) ◽  
pp. 8529-8535 ◽  
Author(s):  
Caixia Xie ◽  
Lei Feng ◽  
Wanli Li ◽  
Xiaojun Ma ◽  
Xinkun Ma ◽  
...  

An efficient and convenient one-pot domino reaction for the direct synthesis of pyrrolo[1,2-a]quinoxalines has been developed. β-Diketones and β-keto esters are well tolerated to give the corresponding products in moderate to excellent yields.

2017 ◽  
Vol 6 (6) ◽  
pp. 746-750 ◽  
Author(s):  
Yi-Bi Xie ◽  
Si-Pei Ye ◽  
Wei-Feng Chen ◽  
Yu-Lin Hu ◽  
De-Jiang Li ◽  
...  

2015 ◽  
Vol 51 (39) ◽  
pp. 8330-8333 ◽  
Author(s):  
Youqiang Lin ◽  
Limin Yang ◽  
Yue Deng ◽  
Guofu Zhong

A chiral cooperative catalysis of NHC and Brønsted acid for a formal [4+2] reaction of unprotected isatins and enals was developed for the direct synthesis of unprotected spiro[indoline-3,2′-pyran]-2,6′(3′H)-diones in good to excellent yields (up to 95%) with high enantioselectivities (up to >93% ee).


ARKIVOC ◽  
2017 ◽  
Vol 2018 (2) ◽  
pp. 81-89
Author(s):  
Abhijeet Srivastava ◽  
Gaurav Shukla ◽  
Dhananjay Yadav ◽  
Maya Shankar Singh

Synthesis ◽  
2018 ◽  
Vol 50 (12) ◽  
pp. 2416-2422 ◽  
Author(s):  
Man-Su Tu ◽  
Guang-Jian Mei ◽  
Feng Shi ◽  
Si-Jia Liu ◽  
Xiao-Li Jiang ◽  
...  

An efficient approach for the synthesis of chromene derivatives from vinyl o-quinone methides was established via a Brønsted acid catalyzed electrocyclization. By using this methodology, a series of structurally diversified chromenes was synthesized in a highly atom-economic and environmentally benign manner with generally good to excellent yields (up to 98% yield). This reaction will not only provide an efficient method for the construction of chromene scaffolds, but also enrich the research area of o-quinone methides.


2018 ◽  
Vol 5 (19) ◽  
pp. 2805-2809 ◽  
Author(s):  
Chang-Bin Yu ◽  
Jie Wang ◽  
Yong-Gui Zhou

A concise synthesis of chiral indolines has been developed through intramolecular condensation, deprotection and palladium-catalyzed asymmetric hydrogenation in a one-pot process with up to 96% ee. A strong Brønsted acid played an important role in both the formation of indoles and asymmetric hydrogenation process.


ACS Omega ◽  
2019 ◽  
Vol 4 (5) ◽  
pp. 9316-9323 ◽  
Author(s):  
Fengbing Liang ◽  
Dawei Chen ◽  
Huizhou Liu ◽  
Weimin Liu ◽  
Mo Xian ◽  
...  

2018 ◽  
Vol 42 (9) ◽  
pp. 463-466 ◽  
Author(s):  
Hao Dong ◽  
Qing Liu ◽  
Yuanyu Tian ◽  
Yingyun Qiao

Tartaric acid–zinc nitrate has been found to be an efficient Brønsted acid-assisted Lewis acid catalytic system for the facile synthesis of β-amino carbonyl compounds through the one-pot Mannich reaction of aldehydes, aromatic amines and ketones in ethanol at room temperature. Remarkable enhancement of reactivity by tartaric acid (Brønsted acid) was observed in these reactions in the presence of anhydrous zinc nitrate (Lewis acid), due to coordination of the tartaric acid ligand to zinc ions increasing the acidity of the system. This procedure shows some advantages such as mild reaction conditions, short reaction times and high yields.


2010 ◽  
Vol 352 (17) ◽  
pp. 2881-2886 ◽  
Author(s):  
Alice Devineau ◽  
Guillaume Pousse ◽  
Catherine Taillier ◽  
Jérôme Blanchet ◽  
Jacques Rouden ◽  
...  

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