Synthesis, rapid resolution, and determination of absolute configuration of racemic 2,2'-binaphthyldiyl crown ethers and analogs via .beta.-cyclodextrin complexation

1985 ◽  
Vol 50 (26) ◽  
pp. 5556-5559 ◽  
Author(s):  
Daniel W. Armstrong ◽  
Timothy J. Ward ◽  
Anna Czech ◽  
Bronislaw P. Czech ◽  
Richard A. Bartsch
1984 ◽  
Vol 32 (4) ◽  
pp. 1662-1664 ◽  
Author(s):  
Kaneto Uekama ◽  
Teruko Imai ◽  
Fumitoshi Hirayama ◽  
Masaki Otagiri ◽  
Kazuaki Harata

2007 ◽  
Vol 70 (8) ◽  
pp. 1339-1343 ◽  
Author(s):  
Karsten Krohn ◽  
Dietmar Gehle ◽  
Sujit Kumar Dey ◽  
Nilufar Nahar ◽  
Mohammed Mosihuzzaman ◽  
...  

1986 ◽  
Vol 51 (8) ◽  
pp. 1731-1742 ◽  
Author(s):  
Josef Hájíček ◽  
Jan Trojánek

A synthesis of (±)-strempeliopine (II) is described, the key step of which is the stereoselective reductive rearrangement of 18-methylene-1,2-dehydroaspidospermidine (XI). The absolute configuration of the natural (-)-base II was determined as (2S, 7R, 20R, 21R) on the basis of its synthesis from (+)-18-methylenevincadifformine (XVII) the configuration of which was derived from a comparison of circular dichroism properties of bases with a β-anilinoacrylate chromophore. The biogenesis of the alkaloids of the schizozygane type is discussed.


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