STEREOSPECIFIC SYNTHESIS OF A DIBENZO[a,g]QUINOLIZINE ANALOG OF 18-HYDROXYALLOYOHIMBANE

1965 ◽  
Vol 43 (9) ◽  
pp. 2545-2550
Author(s):  
B. Belleau ◽  
D. Dvornik

Starting from 4-cyclohexene-cis-1,2-dicarboxylic acid, the stereospecific synthesis of the dibenzo[a,g]quinolizine analog IV of epialloyohimbane is described. The synthetic method of approach is outlined in Chart 1. As the trimethoxybenzoic acid ester, the base IV proved to be devoid of significant pharmacological properties.

1977 ◽  
Vol 8 (11) ◽  
pp. no-no
Author(s):  
H. SCHUBERT ◽  
S. HOFFMANN ◽  
V. UHLIG ◽  
H.-E. POLSTER ◽  
P. HELD ◽  
...  

2018 ◽  
Vol 5 (2) ◽  
pp. 170842 ◽  
Author(s):  
Changkuo Zhao ◽  
Xianheng Wang ◽  
Fuhong Yang ◽  
Lei Gao ◽  
Yuhe Wang

A facile synthetic method was developed for a novel acid-sensitive camptothecin norcantharidin acid ester derivative I . The total yield can reach 71%. This method provides several advantages, including high yield and simple working procedure for the synthesis of analogues. The new synthetic compound I has been shown to exhibit better solubility and similar activity against tumour cell lines.


ChemInform ◽  
2003 ◽  
Vol 34 (23) ◽  
Author(s):  
Yasushi Arakawa ◽  
Tomoaki Murakami ◽  
Yukimi Arakawa ◽  
Shigeyuki Yoshifuji

2003 ◽  
Vol 51 (1) ◽  
pp. 96-97 ◽  
Author(s):  
Yasushi Arakawa ◽  
Tomoaki Murakami ◽  
Yukimi Arakawa ◽  
Shigeyuki Yoshifuji

2021 ◽  
Author(s):  
Eszter Fazekas ◽  
David T Jenkins ◽  
Andrew A Forbes ◽  
Brendan Gallagher ◽  
Georgina Rosair ◽  
...  

A series of amine bisphenol (ABP) pro-ligands featuring amino acid ester pendant arms were prepared. Optimisation of the synthetic method allowed the facile incorporation of naturally occurring, chiral amino acids...


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