A Facile Synthesis of Lentiginosine Analogues Based on a Highly Regio- and Diastereoselective Allylic Amination Using Chlorosulfonyl Isocyanate

2010 ◽  
Vol 2010 (8) ◽  
pp. 1569-1573 ◽  
Author(s):  
In Su Kim ◽  
Qing Ri Li ◽  
Guang Ri Dong ◽  
Yoo Chang Kim ◽  
Yeon Ju Hong ◽  
...  
2013 ◽  
Vol 2013 (20) ◽  
pp. 4427-4433 ◽  
Author(s):  
Qing Ri Li ◽  
Guang Ri Dong ◽  
Sook Jin Park ◽  
Yong Rae Hong ◽  
In Su Kim ◽  
...  

2011 ◽  
Vol 52 (16) ◽  
pp. 1901-1904 ◽  
Author(s):  
Sang Hwi Lee ◽  
In Su Kim ◽  
Qing Ri Li ◽  
Guang Ri Dong ◽  
Young Hoon Jung

ChemInform ◽  
2011 ◽  
Vol 42 (30) ◽  
pp. no-no
Author(s):  
Sang Hwi Lee ◽  
In Su Kim ◽  
Qing Ri Li ◽  
Guang Ri Dong ◽  
Young Hoon Jung

Tetrahedron ◽  
2013 ◽  
Vol 69 (48) ◽  
pp. 10384-10390 ◽  
Author(s):  
Qing Ri Li ◽  
Seung In Kim ◽  
Sook Jin Park ◽  
Hye Ran Yang ◽  
A Reum Baek ◽  
...  

2019 ◽  
Vol 14 (8) ◽  
pp. 828-830 ◽  
Author(s):  
Weihua Meng ◽  
Weihong Wu ◽  
Weiwei Zhang ◽  
Luyao Cheng ◽  
Yunhong Jiao ◽  
...  

Synlett ◽  
1991 ◽  
Vol 1991 (09) ◽  
pp. 725-727 ◽  
Author(s):  
Takeshi Shimizu ◽  
Sayoko Hiranuma ◽  
Zhao-hui Qian ◽  
Hirosuke Yoshioka

2015 ◽  
Vol 12 (1) ◽  
pp. 3910-3918 ◽  
Author(s):  
Dr Remon M Zaki ◽  
Prof Adel M. Kamal El-Dean ◽  
Dr Nermin A Marzouk ◽  
Prof Jehan A Micky ◽  
Mrs Rasha H Ahmed

 Incorporating selenium metal bonded to the pyridine nucleus was achieved by the reaction of selenium metal with 2-chloropyridine carbonitrile 1 in the presence of sodium borohydride as reducing agent. The resulting non isolated selanyl sodium salt was subjected to react with various α-halogenated carbonyl compounds to afford the selenyl pyridine derivatives 3a-f  which compounds 3a-d underwent Thorpe-Ziegler cyclization to give 1-amino-2-substitutedselenolo[2,3-b]pyridine compounds 4a-d, while the other compounds 3e,f failed to be cyclized. Basic hydrolysis of amino selenolo[2,3-b]pyridine carboxylate 4a followed by decarboxylation furnished the corresponding amino selenolopyridine compound 6 which was used as a versatile precursor for synthesis of other heterocyclic compound 7-16. All the newly synthesized compounds were established by elemental and spectral analysis (IR, 1H NMR) in addition to mass spectra for some of them hoping these compounds afforded high biological activity.


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