ChemInform Abstract: Atropisomerism in Natural Products. Absolute Stereochemistry of Biflavone, (-)-4′,4′′′,7,7′′-Tetra-O-methylcupressuflavone, as Determined by the Theoretical Calculation of CD Spectra

ChemInform ◽  
2010 ◽  
Vol 24 (3) ◽  
pp. no-no
Author(s):  
N. HARADA ◽  
H. ONO ◽  
H. UDA ◽  
M. PARVEEN ◽  
N. U.-D. KHAN ◽  
...  
2000 ◽  
Vol 72 (9) ◽  
pp. 1783-1786 ◽  
Author(s):  
Keisuke Suzuki

Strategies and tactics associated with the total synthesis of hybrid natural products are discussed. The target is ravidomycin (2), one of the gilvocarcin-class antitumor antibiotics with an aryl C-glycoside structure. The first total synthesis of 2, which was achieved along similar lines of that of gilvocarcin V (1), served for the determination of the relative as well as the absolute stereochemistry of 2. Also revealed was a limitation of the synthetic scheme so long as the amino sugar congener was concerned. A preliminary result is discussed on the [2+2+2] approach that relies on the ready availability of various benzocyclobutene derivatives via regioselective [2+2] cycloaddition of α-alkoxybenzynes and ketene silyl acetals.


ChemInform ◽  
1987 ◽  
Vol 18 (30) ◽  
Author(s):  
N. HARADA ◽  
H. UDA ◽  
T. NOZOE ◽  
Y. OKAMOTO ◽  
H. WAKABAYASHI ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document