Total Synthesis ofent-Lycoricidineviaa Thiyl Radical Addition−Cyclization Sequence†

1996 ◽  
Vol 61 (24) ◽  
pp. 8366-8367 ◽  
Author(s):  
Gary E. Keck ◽  
Travis T. Wager
Author(s):  
R. G. Gasanov ◽  
R. G. Petrova ◽  
I. O. Bragina ◽  
R. Kh. Freidlina

2019 ◽  
Vol 84 (24) ◽  
pp. 15958-15971
Author(s):  
Pengpeng Zhang ◽  
Yuanhe Li ◽  
Zhiming Yan ◽  
Jianxian Gong ◽  
Zhen Yang

2003 ◽  
Vol 14 (19) ◽  
pp. 2853-2856 ◽  
Author(s):  
Gregory K. Friestad ◽  
Tao Jiang ◽  
Gina M. Fioroni

2008 ◽  
Vol 73 (12) ◽  
pp. 4464-4475 ◽  
Author(s):  
Atsushi Shirai ◽  
Okiko Miyata ◽  
Norimitsu Tohnai ◽  
Mikiji Miyata ◽  
David J. Procter ◽  
...  

2020 ◽  
Vol 142 (30) ◽  
pp. 13227-13234 ◽  
Author(s):  
Haruka Fujino ◽  
Takumi Fukuda ◽  
Masanori Nagatomo ◽  
Masayuki Inoue

2008 ◽  
Vol 80 (4) ◽  
pp. 717-726 ◽  
Author(s):  
Takeaki Naito

A novel synthetic method for the preparation of nitrogen-containing heterocycles via the route involving domino-type radical addition/cyclization reaction of oxime ethers is described. Alkyl radical addition/cyclization of oxime ethers carrying an appropriate leaving group proceeded smoothly to form the alkylated nitrogen-containing heterocyclic compounds. Additionally, tin-mediated radical addition/cyclization/elimination (RACE) reaction of oxime ethers is newly found and successfully applied to an asymmetric total synthesis of (-)-martinellic acid.


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