Heterocyclic Synthesis With Azides. II. The Reaction of Azide With Ethoxymethylenemalonate

1992 ◽  
Vol 45 (11) ◽  
pp. 1781 ◽  
Author(s):  
A Donkor ◽  
RH Prager ◽  
MR Taylor ◽  
MJ Thompson

Sodium azide reacts with diethyl ethoxymethylenemalonate in dimethylsulfoxide to give diethyl 2,4-diethoxycarbonylpent-2-enedioate (12%) and diethyl 5-hydroxypyrrole-2,4-dicarboxyiate (60%). The structure of the latter was determined by X-ray crystal structure analysis at 150 K, and both compounds have been independently synthesized.


1999 ◽  
Vol 23 (9) ◽  
pp. 578-579
Author(s):  
Rainer Schobert ◽  
Hermann Pfab ◽  
Jutta Böhmer ◽  
Frank Hampel ◽  
Andreas Werner

Racemates of (η3-allyl)tricarbonyliron lactone complex Fe(CO)3{η1:η3-C(O)XCH2CHCMeCH2} 1a (X = O) and (η3-allyl)tricarbonyliron lactam complex 2a (X = NMe) are resolved on a preparative scale by HPLC on cellulose tris(3,5-dimethylphenyl)carbamate/silica gel RP-8 and the absolute configuration of (-)-2a is determined by X-ray crystal structure analysis.



2005 ◽  
Vol 88 (4) ◽  
pp. 731-750 ◽  
Author(s):  
Stefan Sahli ◽  
Brian Frank ◽  
W. Bernd Schweizer ◽  
François Diederich ◽  
Denise Blum-Kaelin ◽  
...  




ChemInform ◽  
2010 ◽  
Vol 25 (51) ◽  
pp. no-no
Author(s):  
A. FISCHER ◽  
I. NEDA ◽  
T. KAUKORAT ◽  
R. SONNENBURG ◽  
P. G. JONES ◽  
...  


Molecules ◽  
2017 ◽  
Vol 22 (7) ◽  
pp. 1182 ◽  
Author(s):  
Ji-Hun An ◽  
Alice Kiyonga ◽  
Woojin Yoon ◽  
Hyung Ryu ◽  
Jae-Sun Kim ◽  
...  


1994 ◽  
Vol 29 (3) ◽  
pp. 373-378 ◽  
Author(s):  
Vivek K. Gupta ◽  
K. N. Goswami ◽  
K. K. Bhutani


2007 ◽  
Vol 63 (3) ◽  
pp. o1188-o1189 ◽  
Author(s):  
Wei-Jian Xu ◽  
Yang-Ling Zang ◽  
Guo-Liang Wu ◽  
Sheng-Pei Su ◽  
De-Yue Qiu

The title compound, C14H11BrO, was synthesized by the reaction of 4-methylbenzophenone and bromine in carbon tetrachloride. X-ray crystal structure analysis reveals that the benzene and phenyl rings form a dihedral angle of 59.53 (6)°, and the crystal packing is stabilized by intermolecular C—H...π interactions.



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