Diastereoselective Synthesis oftrans-2,3-Dihydrofurans with Pyridinium Ylide Assisted Tandem Reaction

2009 ◽  
Vol 74 (19) ◽  
pp. 7403-7406 ◽  
Author(s):  
Qi-Fang Wang ◽  
Hong Hou ◽  
Li Hui ◽  
Chao-Guo Yan
Keyword(s):  
Tandem Reaction ◽  
Diastereoselective Synthesis ◽  
Pyridinium Ylide

Diastereoselective Synthesis of N-Aryl Tetrahydroquinolines and N-Aryl Indolines by the Tandem Reaction of Arynes

2014 ◽  
Vol 79 (12) ◽  
pp. 5820-5826 ◽  
Author(s):  
Ji-Xin Pian ◽  
Lin He ◽  
Guang-Fen Du ◽  
Hao Guo ◽  
Bin Dai
Keyword(s):  
Tandem Reaction ◽  
Diastereoselective Synthesis

Theophylline as the catalyst for the diastereoselective synthesis of trans-1,2-dihydrobenzo[a]furo[2,3-c]phenazines in water

RSC Advances ◽  
2016 ◽  
Vol 6 (87) ◽  
pp. 84326-84333 ◽  
Author(s):  
Afshin Yazdani-Elah-Abadi ◽  
Razieh Mohebat ◽  
Malek-Taher Maghsoodlou
Keyword(s):  
Environmentally Benign ◽  
Domino Reaction ◽  
Diastereoselective Synthesis ◽  
Reaction In Water ◽  
Pyridinium Ylide

Theophylline-catalyzed efficient and environmentally benign procedure for the diastereoselective synthesis of trans-1,2-dihydrobenzo[a]furo[2,3-c]phenazines with pyridinium ylide assisted domino reaction in water.

ChemInform Abstract: Diastereoselective Synthesis of N-Aryl Tetrahydroquinolines and N-Aryl Indolines by the Tandem Reaction of Arynes.

ChemInform ◽  
2014 ◽  
Vol 45 (50) ◽  
pp. no-no
Author(s):  
Ji-Xin Pian ◽  
Lin He ◽  
Guang-Fen Du ◽  
Hao Guo ◽  
Bin Dai
Keyword(s):  
Tandem Reaction ◽  
Diastereoselective Synthesis

Efficiently diastereoselective synthesis of functionalized hydro-carbazoles by base-mediated tandem annulation of 1-(2-amino-aryl)prop-2-en-1-ones and sulfur ylide

2020 ◽  
Vol 7 (12) ◽  
pp. 1469-1473 ◽  
Author(s):  
Chengyuan Wang ◽  
Jiong Zhang ◽  
Zheyuan Wang ◽  
Xin-Ping Hui
Keyword(s):  
Tandem Reaction ◽  
Diastereoselective Synthesis ◽  
Unsaturated Ketones ◽  
Sulfur Ylide

The base-promoted [3 + 3]/[1 + 4] tandem reaction of tosyl-protected o-amino α,β-unsaturated ketones and crotonate-derived sulfur ylide is developed for efficiently diastereoselective synthesis of functionalized hydrocarbazoles.

A Brønsted acid catalyzed tandem reaction for the diastereoselective synthesis of cyclobuta-fused tetrahydroquinoline carboxylic esters

2021 ◽  
Author(s):  
Valentina Marras ◽  
Pierluigi Caboni ◽  
Francesco Secci ◽  
Régis Guillot ◽  
David J. Aitken ◽  
...  
Keyword(s):  
Michael Addition ◽  
Tandem Reaction ◽  
Bronsted Acid ◽  
Brønsted Acid ◽  
Diastereoselective Synthesis ◽  
Cyclization Process ◽  
Brönsted Acid ◽  
Acid Catalyzed ◽  
Carboxylic Esters

We have established a Brønsted acid catalyzed diastereoselective synthesis of diversely substituted cyclobuta-fused tetrahydroquinoline carboxylic esters through a new tandem aza-Michael addition-aza-Friedel–Crafts cyclization process.

Diastereoselective synthesis ofcis-1,3-disubstituted isoindolinesviaa highly site-selective tandem cyclization reaction

2018 ◽  
Vol 5 (12) ◽  
pp. 1950-1956 ◽  
Author(s):  
Siyang Xing ◽  
Hong Cui ◽  
Jiajing Qin ◽  
Nan Gu ◽  
Bowei Zhang ◽  
...  
Keyword(s):  
Michael Addition ◽  
Ring Opening ◽  
Cyclization Reaction ◽  
Tandem Reaction ◽  
Diastereoselective Synthesis ◽  
Tandem Cyclization ◽  
Site Selective

A highly site-selective tandem reaction involving regioselective ring opening of aziridines and Michael addition of electron-deficient alkenes has been described.

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