ChemInform Abstract: ABSOLUTE STEREOCHEMISTRY OF (+)-1,8A-DIHYDRO-3,8-DIMETHYLAZULENE, A LABILE BIOSYNTHETIC INTERMEDIATE FOR 1,4-DIMETHYLAZULENE. DETERMINATION BY THEORETICAL CALCULATION OF CD SPECTRA AND VERIFICATION BY SYNTHESIS OF MODEL COMPOUNDS

1985 ◽  
Vol 16 (21) ◽  
Author(s):  
N. HARADA ◽  
J. KOHORI ◽  
H. UDA ◽  
K. NAKANISHI ◽  
R. TAKEDA
ChemInform ◽  
1987 ◽  
Vol 18 (30) ◽  
Author(s):  
N. HARADA ◽  
H. UDA ◽  
T. NOZOE ◽  
Y. OKAMOTO ◽  
H. WAKABAYASHI ◽  
...  

2000 ◽  
Vol 65 (10) ◽  
pp. 1643-1652
Author(s):  
Radek Pohl ◽  
Jan Sýkora ◽  
Petr Maloň ◽  
Stanislav Böhm ◽  
Bohumil Kratochvíl ◽  
...  

The absolute configuration of the atropisomeric (Z)-3-(5-methyl-2-phenylimidazo[1,2-a]pyridin-3-yl)-1,3-diphenylprop-2-en-1-one was evaluated to be R for the dextrorotatory and S for the laevorotatory enantiomers. The assignment is based on their two-step syntheses via atropodiastereoisomeric carbamates prepared from the corresponding atropodiastereoisomeric alcohols with (R)-(+)-α-phenylethyl isocyanate and by a complete X-ray space analysis of the quaternary triiodide obtained from the (R)-(+)-enantiomer. CD spectra and PM3 calculated heats of formation for selected compounds are discussed in relation to the found molecular configurations.


1992 ◽  
Vol 25 (23) ◽  
pp. 6322-6331 ◽  
Author(s):  
Yeong Soo Oh ◽  
Toshimasa Yamazaki ◽  
Murray Goodman

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