Metal-Free Stereoselective Synthesis of (E)- and (Z)-N-Monosubstituted β-Aminoacrylates via Condensation Reactions of Carbamates

Author(s):  
Scott R. Pollack ◽  
Amélie Dion
Synlett ◽  
2021 ◽  
Author(s):  
Yuling Mei ◽  
nan jiang ◽  
Yu Yang ◽  
Wan Zhang ◽  
Saifeng Qiu ◽  
...  

A convenient protocol for β-stereoselective synthesis of 2-deoxy-C-aryl glycosides has been developed. This reaction takes place in one step by using I2/Et3SiH to activate glycosyl acetate to generate glycosyl iodide intermediate in situ, which was captured by naphthol followed by Fries-like O- → C-glycoside rearrangement to selectively afford β-C-aryl glycoside. The approach is applicable to a wide range of naphthol modules, and its utility was demonstrated in the synthesis of 5-aza analogues of Aquayamycin.


Molecules ◽  
2019 ◽  
Vol 24 (12) ◽  
pp. 2260
Author(s):  
Margherita Pirola ◽  
Alessandra Puglisi ◽  
Laura Raimondi ◽  
Alessandra Forni ◽  
Maurizio Benaglia

A stereoselective synthetic strategy for the preparation of trifluoromethylamine mimics of retro-thiorphan, involving a diastereoselective, metal-free catalytic step, has been studied in batch and afforded the target molecule in good yields and high diastereoselectivity. A crucial point of the synthetic sequence was the catalytic reduction of a fluorinated enamine with trichlorosilane as reducing agent in the presence of a chiral Lewis base. The absolute configuration of the key intermediate was unambiguously assigned by X-ray analysis. The synthesis was also investigated exploiting continuous flow reactions; that is, an advanced intermediate of the target molecule was synthesized in only two in-flow synthetic modules, avoiding isolation and purifications of intermediates, leading to the isolation of the target chiral fluorinated amine in up to an 87:13 diastereoisomeric ratio.


2020 ◽  
Vol 9 (7) ◽  
pp. 1040-1044 ◽  
Author(s):  
Ya‐Nan Wu ◽  
Tian‐Shu Zhang ◽  
Wen‐Juan Hao ◽  
Shu‐Jiang Tu ◽  
Bo Jiang

Molecules ◽  
2019 ◽  
Vol 24 (19) ◽  
pp. 3594 ◽  
Author(s):  
Muzalevskiy ◽  
Sizova ◽  
Belyaeva ◽  
Trofimov ◽  
Nenajdenko

The reaction of pyridines with trifluoroacetylated acetylenes was investigated. It was found that the reaction of various pyridines with two molecules of CF3CO-acetylenes proceeds under mild metal-free conditions. As a result, efficient stereoselective synthesis of 3-arylethynyl-3-trifluoromethyl-1,3-oxazinopyridines was elaborated. Target heterocycles can be prepared in up to quantitative yields.


2017 ◽  
Vol 58 (31) ◽  
pp. 3003-3007 ◽  
Author(s):  
Xufeng Nie ◽  
Yachuan Wang ◽  
Lijun Yang ◽  
Zaijun Yang ◽  
Tairan Kang

2019 ◽  
Vol 10 (1) ◽  
Author(s):  
Bo Zhou ◽  
Ying-Qi Zhang ◽  
Kairui Zhang ◽  
Ming-Yang Yang ◽  
Yang-Bo Chen ◽  
...  

2019 ◽  
Vol 58 (26) ◽  
pp. 8779-8783 ◽  
Author(s):  
Mindaugas Šiaučiulis ◽  
Nanna Ahlsten ◽  
Alexander P. Pulis ◽  
David J. Procter

2021 ◽  
Vol 57 (75) ◽  
pp. 9542-9545
Author(s):  
Budaganaboyina Prasad ◽  
Mandalaparthi Phanindrudu ◽  
Jagadeesh Babu Nanubolu ◽  
Ahmed Kamal ◽  
Dharmendra Kumar Tiwari

We report herein our observation of an unprecedented stereoselective synthesis of 2H-isoindolin-1,3-ylidenes from 2-formylphenyl acrylates and phenacylazide in the presence of piperidine.


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