scholarly journals "It’s a (Kinetic) Trap!" – Selectively Differentiating Allylic Azide Isomers

Synlett ◽  
2018 ◽  
Vol 29 (12) ◽  
pp. 1537-1542 ◽  
Author(s):  
Joseph Topczewski ◽  
Matthew Porter

Allylic azides are known to undergo the Winstein rearrangement and are often isolated as an equilibrating mixture of isomers. While this process has been known for almost 60 years, very few synthetic applications of this process have been reported. The absence of methods exploiting these intermediates likely stems from a paucity of approaches for gaining the required selectivity to differentiate the isomers. Our lab has made some progress in leveraging this unusual reaction into practical synthetic methodology. Presented herein is a summary of our lab’s recent accomplishments in selectively trapping allylic azides.1 Introduction2 Background: Allylic Azides3 Dynamic Cyclization of Imidates4 Summary and Outlook

2020 ◽  
Vol 24 (18) ◽  
pp. 2181-2191
Author(s):  
Li Wang ◽  
Ziyi Li ◽  
Jiang Liu ◽  
Jianlin Han ◽  
Hiroki Moriwaki ◽  
...  

The development of an efficient and mild synthetic methodology for the construction of bioactive fluorine-containing molecules represents one of the hot research topics in general synthetic organic chemistry. In this review, some recent progresses achieved in the development of detrifluoroacetylatively generated mono-fluorinated enolates via CC bond cleavage and their asymmetric nucleophilic reactions for assembly of chiral quaternary C-F center containing compounds.


2021 ◽  
Author(s):  
Hui-Min Wu ◽  
Zongpeng Zhang ◽  
Liang Wei ◽  
Xiu-Qin Dong ◽  
Chun-Jiang Wang

An efficient synthetic methodology to access biologically important and synthetically useful α-quaternary cysteine derivatives via asymmetric catalytic α-allylation of readily available 2-thiazoline-4-carboxylates was successfully developed through the synergistic Cu/Pd catalytic...


Synthesis ◽  
2020 ◽  
Author(s):  
Peter Ehlers ◽  
Peter Langer ◽  
Marian Blanco Ponce ◽  
Silvio Parpart ◽  
Alexander Villinger ◽  
...  

AbstractA concise and modular synthesis of pyrrolo[1,2-a][1,6]- and [1,8]naphthyridines by a one-pot two-step reaction consisting of electrophilic acylation followed by an alkyne-carbonyl-metathesis reaction as the final cyclization step is reported. This developed synthetic methodology allows the facile synthesis of these heterocyclic core structures in mainly high overall yields under metal-free conditions. Reaction conditions are carefully optimized and display a novel supplement to access these tricyclic heterocyclic compounds.


Catalysts ◽  
2021 ◽  
Vol 11 (5) ◽  
pp. 646
Author(s):  
Victorio Cadierno

The use of organometallic compounds in organic chemistry is one of the cornerstones of the modern synthetic methodology for the activation and generation of new bonds in a molecule [...]


ChemInform ◽  
1990 ◽  
Vol 21 (23) ◽  
Author(s):  
R. W. CARLING ◽  
N. R. CURTIS ◽  
A. B. HOLMES

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