✦ LIBER ✦

1H-NMR, Ultraviolet and infrared spectra of some (Z)-α-(phenyl)-β-(2-furyl), -(2-pyrrolyl) and -(N-methyl-2-pyrrolyl)acrylonitriles

✍ Scribed by Gaetano Alberghina; Maria Emanuela Amato; Francesco Agatino Bottino; Antonino Corsaro; Salvatore Fisichella

Book ID: 112128421
Publisher: Journal of Heterocyclic Chemistry
Year: 1986
Tongue: English
Weight: 469 KB
Volume: 23
Category: Article
ISSN: 0022-152X
DOI: 10.1002/jhet.5570230629

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Infrared and ultraviolet spectra of some

Infrared and ultraviolet spectra of some (Z)-α-phenyl-β(2-thienyl) acrylonitriles

✍ M.E. Amato; D. Carbone; S. Fisichella; G. Scarlata 📂 Article 📅 1982 🏛 Elsevier Science 🌐 English ⚖ 173 KB

NMR stereospecific long-range coupling a

NMR stereospecific long-range coupling and preferred conformations in some (E)- and (Z)-α-phenyl-β-[2-(N-methyl)nitropyrrolyl] acrylic acids

✍ Francesco A. Bottino; Giovanni Mineri; Domenico Sciotto 📂 Article 📅 1978 🏛 Elsevier Science 🌐 French ⚖ 220 KB

Total assignment of 1H and 13C spectra o

Total assignment of 1H and 13C spectra of the chlorinated triterpenoid (methyl 2α,3β,24-tri-O-acetylolean-12α- chloro-28,13β-olide) by NMR spectroscopy

✍ F. J. Q. Monte; J. P. Kintzinger; R. Braz-Filho 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 185 KB 👁 1 views

The current substantial interest concerning the structure elucidation of new active natural products led to the complete 1H and 13C chemical shift assignment of a triterpenoid derivative, methyl 2a,3b,24-tri-Oacetylolean-12a-chloro-28,13b-olide, obtained after acetylation and methylation of a mixtur

1H n.m.r. spectra of some bicyclic compo

1H n.m.r. spectra of some bicyclic compounds: I—relative configurations of the diastereomeric endo-α-methyl-5-norbornene-2-methanols, the corresponding saturated analogues, and their cyclization ether products

✍ M. Lj. Mihailović; S. Milosavljević; D. Jeremić; J. Milovanović 📂 Article 📅 1977 🏛 John Wiley and Sons 🌐 English ⚖ 553 KB

## Abstract The configurational and conformational relationship at C‐2 and C‐α in the two racemic diastereomeric __endo__‐α‐methyl‐5‐norbornene‐2‐methanols and the corresponding saturated __endo__‐α‐methyl‐2‐norbornanemethanols were determined by first‐order analysis of the ^1^H n.m.r. spectra of t