✦ LIBER ✦

Reaction of the Fischer base with 8-hydroxy-1-naphthaldehydes. Investigation of the reaction products by13C NMR spectroscopy

✍ Scribed by Yu. M. Chunaev; N. M. Przhiyalgovskaya; L. N. Kurkovskaya; M. A. Gal'bershtam

Book ID: 112348981
Publisher: Springer US
Year: 1982
Tongue: English
Weight: 561 KB
Volume: 18
Category: Article
ISSN: 0009-3122
DOI: 10.1007/bf00506365

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

The reaction of azibenzil with sulfur di

The reaction of azibenzil with sulfur dioxide: structural revision and its proof by 13C NMR spectroscopy

✍ J.B. Stothers; L.J. Danks; J.F. King 📂 Article 📅 1971 🏛 Elsevier Science 🌐 French ⚖ 181 KB

It has been reported' that the reaction of azibenxil (1) and sulfur dioxide leads amongst other materials to two new products which were assigned structures 4 and 5. These -W

Products of the Base-catalyzed Reaction

Products of the Base-catalyzed Reaction of Benzophenone with Dimethyl Sulfoxide 1

✍ Walling, Cheves; Bollyky, Laszlo 📂 Article 📅 1963 🏛 American Chemical Society 🌐 English ⚖ 295 KB

Investigation of the structure of the pr

Investigation of the structure of the products from telomerization of ethylene with 1,3-diheterocyclopentanes by the13C NMR method

✍ A. V. Germash; V. I. Dostovalova; V. V. Zorin; A. B. Terent'ev 📂 Article 📅 1983 🏛 Springer 🌐 English ⚖ 375 KB

Identification of structure and study of

Identification of structure and study of configuration of reaction products of endo-dicyclopentadiene with phenols by the1H and13C NMR method

✍ V. P. Lezina; A. U. Stepanyants; A. S. Murakhovskaya; V. R. Melikyan; L. L. Vasi 📂 Article 📅 1974 🏛 Springer 🌐 English ⚖ 211 KB

Reaction of o-phenylenediamine with diac

Reaction of o-phenylenediamine with diacetyl monoxime: characterisation of the product by solid-state 13C and 15N MAS NMR

✍ T. Radhakrishnan; P. Sreekumari Nair; G. A. Kolawole; N. Revaprasadu; G. E. Hawk 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 217 KB

## Abstract 2,3‐Dimethylquinoxaline (DMQ) and dimethylglyoxime (DMGH~2~) form a 1:1 hydrogen‐bonded complex in the solid state, which is completely dissociated in methanol solution. There are small differences in solid‐state ^13^C shifts between the separated components DMQ and DMGH~2~ and the comp

1H and 13C NMR spectral studies of some

1H and 13C NMR spectral studies of some biquinoline derivatives and a re-investigation of the reaction of quinoline with sodium

✍ Alan G. Osborne; Richard Green; Ian H. Sadler; David Reed 📂 Article 📅 1989 🏛 John Wiley and Sons 🌐 English ⚖ 738 KB