ChemInform Abstract: Abnormal Diels-Alder Reaction of Oxazoles with 4-Phenyl-3H-1,2,4- triazole-3,5(4H)-dione and Diethyl Azodicarboxylate, and X-Ray Crystal Structure of an Adduct.

ChemInform ◽  
2010 ◽  
Vol 24 (10) ◽  
pp. no-no
Author(s):  
T. IBATA ◽  
H. SUGA ◽  
Y. ISOGAMI ◽  
H. TAMURA ◽  
X. SHI
ChemInform ◽  
2010 ◽  
Vol 23 (44) ◽  
pp. no-no
Author(s):  
T. IBATA ◽  
Y. ISOGAMI ◽  
H. NAKAWA ◽  
H. TAMURA ◽  
H. SUGA ◽  
...  

2003 ◽  
Vol 81 (11) ◽  
pp. 1180-1186 ◽  
Author(s):  
Laura E Harrington ◽  
James F Britten ◽  
Michael J McGlinchey

3-Ferrocenyl-2,4,5-tri-(β-naphthyl)cyclopentadienone undergoes a Diels–Alder reaction with di-(β-naphthyl) acetylene to yield, after elimination of carbon monoxide, ferrocenyl-penta-(β-naphthyl)benzene (4). 1H and 13C variable-temperature NMR studies on 4 reveal the existence of multiple diastereoisomers at low temperature. These data are interpreted in terms of slowed rotation of the naphthyl groups, and are supported by the X-ray crystal structure of 4, which exhibits disorder at three of the naphthyl sites.Key words: sterically crowded molecules, hindered rotations, crystallography, NMR.


2020 ◽  
Vol 17 (8) ◽  
pp. 624-627
Author(s):  
Sujata V. Bhat ◽  
Rohan S. Pawar ◽  
P. Rajakannu

One-pot tandem oxidation and double Diels-Alder reaction of myrcene or ocimene with in situ generated 1,4-benzoquinone or 1,2-benzoquinone at 0°C for 1.5 h yielded polyalkylated 1,4,4a,5,8,8a,9a,10a-octahydro-9,10-anthracenediones and bis(alkylated) 9,10-phenanthrenedione respectively. The structure of novel bis-adduct from ocimene, (1R,4aR,5S,8aS,9aS,10aR)-rel- 1,4,4a,5,8,8a,9a,10a-octahydro-2,6-dimethyl-1,5-bis(3-methyl-2-buten-1-yl)-9,10-anthracenedione, was elucidated through single crystal X-ray analysis.


1992 ◽  
Vol 65 (7) ◽  
pp. 1771-1778 ◽  
Author(s):  
Toshikazu Ibata ◽  
Yasushi Isogami ◽  
Hiroyuki Nakawa ◽  
Hatsue Tamura ◽  
Hiroyuki Suga ◽  
...  

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