Molecular and crystal structure of the methyl ester of 2-chloromercuri-3-trifluoroacetoxy-2,3-diphenylcyclopropane-1-carboxylic acid

1988 ◽  
Vol 28 (5) ◽  
pp. 726-730
Author(s):  
L. G. Kuz'mina ◽  
Yu. T. Struchkov ◽  
A. N. Chernov ◽  
V. R. Kartashov ◽  
N. V. Malisova ◽  
...  
2017 ◽  
Vol 232 (3) ◽  
pp. 409-410
Author(s):  
Wen-Jing Hao ◽  
Xiao-Yan Xu ◽  
Dai-Zun Zhang ◽  
Rui Han

AbstractC21H25NO5, monoclinic, P21/n (no. 14) a = 10.4501(19) Å, b = 15.750(3) Å, c = 12.043(2) Å, β = 102.625(3)°, V = 1934.3(6) Å3, Z = 4, Rgt(F) = 0.0406, wRref(F2) = 0.1177, T = 296(2) K.


2013 ◽  
Vol 2013 ◽  
pp. 1-9 ◽  
Author(s):  
Hui-Jing Li ◽  
Jun-Li Wang ◽  
Rui Wang ◽  
Dong-Hui Luo ◽  
Yan-Chao Wu

4H-Chromene-2-carboxylic acid ester derivatives of renieramycin M might be of use for the structural-activity relationship studies of antitumor antibiotic tetrahydroisoquinoline natural products. Accordingly, 6-tert-butyl-4-phenyl-4H-chromene-2-carboxylic acid, one key intermediate, was synthesized via the condensation of (3E)-2-oxo-4-phenylbut-3-enoate methyl ester with 4-tert-butylphenol in the presence of AuCl3/3AgOTf (5 mol%), followed by cyclodehydration and aqueous hydrolysis. The product was unambiguously shown to the 4H-chromene-2-carboxylic acid by spectroscopy and X-ray crystallographic analysis. A packing diagram of the crystal structure shows that aromaticπ-stacking interactions and O–H⋯O hydrogen bond stabilize the structure in the solid.


1998 ◽  
Vol 51 (5) ◽  
pp. 347 ◽  
Author(s):  
Melvyn Gill ◽  
Malcolm S. Buchanan ◽  
Peter J. Steel ◽  
Nives M. Milanovic ◽  
Somphone Phonh-Axa

Clavorubin (1,5,6,8-tetrahydroxy-3-methyl-9,10-dioxoanthracene-2-carboxylic acid) (1), previously known only from the ascomycetious rye fungus Claviceps purpurea (‘ergot’), has been isolated from the fruit bodies of two Australasian basidiomycetes belonging to the genus Cortinarius and characterized by spectroscopic and chemical methods. A single-crystal X-ray structure analysis of the methyl ester (4) of 6-O-methylclavorubin establishes unequivocally, for the first time, the structure of the natural product.


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