Chemistry of phosphodiesters, DNA and models. 5. Microgonotropens and their interactions with DNA. 3. Structural analysis of the 1:1 complex of d(CGCAAATTTGCG)2 and dien-microgonotropen-c by 2D NMR spectroscopy and restrained molecular modeling

1993 ◽  
Vol 115 (16) ◽  
pp. 7080-7092 ◽  
Author(s):  
Andrei Blasko ◽  
Kenneth A. Browne ◽  
Gong Xin He ◽  
Thomas C. Bruice
1991 ◽  
Vol 1991 (12) ◽  
pp. 1337-1341 ◽  
Author(s):  
Horst Kessler ◽  
Siggi Mronga ◽  
Bernhard Kutscher ◽  
Arndt Müller ◽  
William S. Sheldrick

2012 ◽  
Vol 7 (11) ◽  
pp. 1934578X1200701 ◽  
Author(s):  
David Paniagua-Vega ◽  
Carlos M. Cerda-García-Rojas ◽  
Teresa Ponce-Noyola ◽  
Ana C. Ramos-Valdivia

Chemical studies on Hamelia patens (Rubiaceae) micropropagated plantlets allowed production of a new monoterpenoid oxindole alkaloid, named (–)-hameline (7), together with eight known alkaloids, tetrahydroalstonine (1), aricine (2), pteropodine (3), isopteropodine (4), uncarine F (5), speciophylline (6), palmirine (8), and rumberine (9). The structure of the new alkaloid was assigned on the basis of 1D and 2D NMR spectroscopy, mass spectrometry, and molecular modeling.


2018 ◽  
Vol 545 (1-2) ◽  
pp. 357-365 ◽  
Author(s):  
Saugat Adhikari ◽  
Saloni Daftardar ◽  
Filip Fratev ◽  
Miguel Rivera ◽  
Suman Sirimulla ◽  
...  

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