scholarly journals Artificial Erythrina Alkaloids from Three Erythrina Plants, E. variegata, E. crista-galli and E. arborescens

2020 ◽  
Vol 10 (2) ◽  
pp. 57-66
Author(s):  
Bing-Jie Zhang ◽  
Jing Wu ◽  
Mei-Fen Bao ◽  
Fang Wang ◽  
Xiang-Hai Cai
Keyword(s):  
Planta Medica ◽  
2013 ◽  
Vol 79 (13) ◽  
Author(s):  
M Soto-Hernandez ◽  
R Garcia-Mateos ◽  
R San Miguel Chavez ◽  
G Kite
Keyword(s):  

1949 ◽  
Vol 71 (3) ◽  
pp. 875-878 ◽  
Author(s):  
Frank. Koniuszy ◽  
Paul F. Wiley ◽  
Karl. Folkers
Keyword(s):  

1942 ◽  
Vol 64 (9) ◽  
pp. 2146-2151 ◽  
Author(s):  
Karl Folkers ◽  
Frank Koniuszy ◽  
John Shavel
Keyword(s):  

1966 ◽  
pp. 142 ◽  
Author(s):  
J. E. Gervay ◽  
F. McCapra ◽  
T. Money ◽  
G. M. Sharma ◽  
A. I. Scott

Synlett ◽  
2020 ◽  
Vol 31 (04) ◽  
pp. 327-333 ◽  
Author(s):  
Jesper L. Kristensen ◽  
Sebastian Clementson ◽  
Mikkel Jessing ◽  
Paulo J. Vital

Erythrina alkaloids were identified at the end of the 19th century and today, more than 100 members of the erythrinane family have been isolated. They are characterized by a unique tetracyclic, α-tertiary spiroamine scaffold. Herein we detail our efforts towards the development of a divergent enantioselective synthesis of (+)-dihydro-β-erythroidine (DHβE) – one of the most prominent members of this intriguing family of natural products.1 Introduction2 Synthetic Strategy2.1 First Generation2.2 Second Generation2.3 Third Generation2.3.1 Radical Endgame2.3.2 Completion of the Total Synthesis3 Conclusion


Synfacts ◽  
2016 ◽  
Vol 12 (08) ◽  
pp. 0777-0777

1971 ◽  
Vol 10 (6) ◽  
pp. 411-412 ◽  
Author(s):  
Burchard Franck ◽  
Volker Teetz

ChemInform ◽  
2007 ◽  
Vol 38 (15) ◽  
Author(s):  
Eberhard Reimann
Keyword(s):  

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