Molecular structure of the exo-Diels-Alder-adduct of 5-methoxy-2-methyl-4-(p-nitrophenyl)oxazole with N-methylmaleimide.
スポンサーリンク
概要
- 論文の詳細を見る
The molecular structure of the exo-Diels–Alder adduct of 5-methoxy-2-methyl-4-(<I>p</I>-nitrophenyl)oxazole with <I>N</I>-methylmaleimide was determined by X-ray analysis. The crystals are triclinic, space group <I>P</I>\bar1, with <I>a</I>=9.160(2), <I>b</I>=11.182(2), <I>c</I>=8.816(1) Å, α=92.39(1), β=116.47(1), γ=100.60(1)°, <I>Z</I>=2, <I>D</I><SUB>x</SUB>=1.455 Mg m<SUP>−3</SUP>, <I>D</I><SUB>m</SUB>=1.458 Mg m<SUP>−3</SUP>, μ(Cu <I>K</I>α)=9.76 cm<SUP>−1</SUP>. The configuration of the exo-adduct is consistent with that predicted on the basis of the NMR data.
- 公益社団法人 日本化学会の論文
著者
-
TOYODA Jiro
Institute for Molecular Science
-
Ibata Toshikazu
Institute Of Chemistry College Of General Education Osaka University
-
TAMURA Hatsue
Institute of Chemistry, College of General Education, Osaka University
-
Ogawa Kazuhide
Institute of Chemistry, College of General Education, Osaka University
関連論文
- Dimeric Hydrogen - Bonded Transition Metal Complex Containing Bidentate Mono - deprotonated 2,2'-Biimidazolate Ligand
- Synthesis and Properties of 1,6-Diselenapyrene (DSPY) and Its Methyl Chalcogeno Derivatives
- Hydrogen-bonded Charge-Transfer Complex of Ethylenediaminoglyoxime Transition Metal Complex with Tetracyanoquinodimethane
- Nucleophilic Substitution Reaction of Aromatic Chlorides with Cyclic Tertiary Amines under High Pressure
- Formation and Reaction of Azomethine Ylide by the Reaction of Cu(acac)2-ketocarbenoids with 1,1-Diphenylmethanimine
- X-Ray Molecular Structure of [NBu^n_4]_2[Mo(C_3S_5)_3] and Electrical Conductivities of the Oxidized Species
- Formation and Reaction of Acyl Substituted Nitrile Ylide through the Rh_2(OAc)_4-Catalyzed Reaction of α-Diazocarbonyl Compounds with Benzonitrile
- Molecular structure of the exo-Diels-Alder-adduct of 5-methoxy-2-methyl-4-(p-nitrophenyl)oxazole with N-methylmaleimide.
- Synthesis and molecular structure of the 2:1-cycloadduct of 1-methoxy-2-benzopyrylium-4-olate with acenaphthylene.
- The BF3 catalyzed decomposition of diazo compounds in the presence of carbonyl compounds.
- The reaction of diazo ketones in the presence of metal chelates. VIII. The stereochemistry of the 1,3-dipolar cycloaddition of 1-methoxy-2-benzopyrylium-4-olates to ethylenic dipolarophiles.
- Formation and reaction of oxazoles. Synthesis of N-substituted 2-(aminomethyl)oxazoles.
- Aromatic nucleophilic substitution of halobenzenes with amines under high pressure.
- Reaction of diazo ketones in the presence of metal chelates. VII. 1,3-Dipolar cycloaddition of 1-methoxybenzo[c]pyrylium-4-olate with acetylenic dipolarophiles.
- The acid catalyzed decomposition of diazo compounds. I. Synthesis of oxazoles in the BF3 catalyzed reaction of diazo carbonyl compounds with nitriles.
- Formation of 1,3-oxathiole-2-thione and 1,2,4-trithiolane derivatives by the catalytic reaction of .ALPHA.-diazocarbonyl compounds with carbon disulfide.
- Formation and molecular structure of the 2:1-adducts of 1-alkoxy-2-benzopyrylium-4-olates with carbon disulfide.
- The Diels-Alder reactions of 2-alkyl-5-methoxy-4-(p-nitrophenyl)oxazoles with ethylenic, acetylenic, and azo-type dienophiles.
- The Acid-catalyzed Decomposition of α-Diazo β-Hydroxy Ketones
- Formation and reaction of carbonyl ylides. 1,3-Dipolar cycloaddition of 2-benzopyrylium-4-olates with carbonyl compounds.
- The high pressure Diels-Alder reactions of 5-methoxy-2-methyl-4-(p-nitrophenyl)oxazole with ethylenic dienophiles.
- The acid-catalyzed decomposition of diazo carbonyl compounds. II. Synthesis of 2- or 5-heteroatom-substituted oxazoles.