✦ LIBER ✦

Mass spectra of 4-substituted-1,2,6-trimethyl-3,5-diethoxycarbonyl-1,4-dihydropyridines

✍ Scribed by E. L. Esmans; R. A. Dommisse; F. C. Alderweireldt

Publisher: John Wiley and Sons
Year: 1975
Tongue: English
Weight: 198 KB
Volume: 10
Category: Article
ISSN: 1076-5174
DOI: 10.1002/oms.1210101008

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

The antioxidant acitivity of 2,6-dimethy

The antioxidant acitivity of 2,6-dimethyl-3,5-diethoxycarbonyl-1,4-dihydropyridine in edible oils

✍ Kouřimská, L. ;Pokorný, J. ;Tirzitis, G. 📂 Article 📅 1993 🏛 John Wiley and Sons 🌐 English ⚖ 141 KB

The Molecular Structure of 3,5-Diethoxyc

The Molecular Structure of 3,5-Diethoxycarbonyl-2, 6-Dimethyl-1,4-Dihydropyridine. An X-Ray Study

✍ A. T. H. Lenstra; G. H. Petit; R. A. Dommisse; F. C. Alderweireldt 📂 Article 📅 2010 🏛 Wiley (John Wiley & Sons) ⚖ 477 KB 👁 2 views

Synthesis of Some C-3,4,5-Substituted 2,

Synthesis of Some C-3,4,5-Substituted 2,6-Dimethyl-1,4-dihydropyridines (4-DHPs)

✍ Patricio A. Navarette-Encina; Juan A. Squella; J. Carbajo; B. Conde; Luis J. Nun 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 18 KB 👁 1 views

1-Acetyl-2,4,5-trimethyl-3,6-diazaphenan

1-Acetyl-2,4,5-trimethyl-3,6-diazaphenanthrene

✍ Klaus Gorlitzer; Dietrich Buß 📂 Article 📅 1985 🏛 John Wiley and Sons 🌐 English ⚖ 255 KB 👁 2 views

Mass spectra of some 2-(4′-butyl-3,′5′-d

Mass spectra of some 2-(4′-butyl-3,′5′-dimethylpyrazol-1′-yl)-6-substituted benzothiazoles

✍ Shiv P. Singh; Radhe K. Vaid 📂 Article 📅 1986 🏛 John Wiley and Sons 🌐 English ⚖ 289 KB

Electron-impact mass spectra of substitu

Electron-impact mass spectra of substituted 1-alkyl-2-arylsulphonylamino-1,4,5,6-tetrahydropyrimidines

✍ Vladimir Ovcharenko; Elzbieta Szacon; Tadeusz Tkaczynski; Dariusz Matosiuk; Kale 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 88 KB 👁 1 views

Fragmentation pathways of the title compounds under electron impact were compared to those of their (1aryl)substituted analogs reported earlier. The main fragmentation route of the M Á ions is the sulphamide N-S bond cleavage leading to [M À ArSO 2 ] ions. No loss of the alkyl substituents from the