Synthesis of Chiral Acyclic Nucleosides by Sharpless Asymmetric Dihydroxylation: Access to Cidofovir and Buciclovir

2018 ◽  
Vol 83 (24) ◽  
pp. 15512-15523 ◽  
Author(s):  
Tao Qin ◽  
Jian-Ping Li ◽  
Ming-Sheng Xie ◽  
Gui-Rong Qu ◽  
Hai-Ming Guo
2020 ◽  
Author(s):  
Hui Zhao ◽  
Kai Gao ◽  
Haichen Ma ◽  
Tsz Chun Yip ◽  
Wei-Min Dai

The C19–C30 bis-THF fragment of the proposed structure of iriomoteolide-13a has been synthesized. The w-mesyloxy-substituted stereotetrad possessing three continuous hydroxy groups was generated by <i>anti</i>-aldol reaction and asymmetric dihydroxylation (AD). Upon heating in pyridine the stereotetrad underwent an S<sub>N</sub>2 cyclization to form the C19–C22 THF ring. It was followed by an intramolecular <i>syn</i>-oxypalladation of the C28 chiral allylic alcohol to give the C23–C26 THF ring.


2015 ◽  
Vol 12 (9) ◽  
pp. 1603-1612 ◽  
Author(s):  
Mohammad Navid Soltani Rad ◽  
Somayeh Behrouz ◽  
Elham Zarenezhad ◽  
Narjes Kaviani

1992 ◽  
Vol 33 (43) ◽  
pp. 6411-6414 ◽  
Author(s):  
Ehud Keinan ◽  
Subhash C. Sinha ◽  
Anjana Sinha-Bagchi ◽  
Wang Zhi-Min ◽  
Zhang Xiu-Lian ◽  
...  

ChemInform ◽  
2010 ◽  
Vol 33 (4) ◽  
pp. no-no
Author(s):  
Boyapati M. Choudary ◽  
Naidu S. Chowdari ◽  
Mannepalli L. Kantam ◽  
Kondapuram V. Raghavan

ChemInform ◽  
2010 ◽  
Vol 25 (33) ◽  
pp. no-no
Author(s):  
A. R. BASSINDALE ◽  
P. G. TAYLOR ◽  
Y. XU

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