✦ LIBER ✦

The influence of cis-groups on the rate of the trans-substitution reaction

✍ Scribed by I. B. Bersuker

Book ID: 104922912
Publisher: SP MAIK Nauka/Interperiodica
Year: 1964
Tongue: English
Weight: 240 KB
Volume: 4
Category: Article
ISSN: 0022-4766
DOI: 10.1007/bf00745553

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Influence of alkyl substitution on the t

Influence of alkyl substitution on the trans .fwdarw. cis photoisomerization of all-trans-retinal and related polyenes

✍ Waddell, Walter H.; Hopkins, Daniel L.; Uemura, Motokazu; West, John L. 📂 Article 📅 1978 🏛 American Chemical Society 🌐 English ⚖ 407 KB

Direct measurement of the reaction rate

Direct measurement of the reaction rate for cis → trans photoisomerization of stilbene

✍ Minoru Sumitani; Nobuaki Nakashima; Keitaro Yoshihara 📂 Article 📅 1979 🏛 Elsevier Science 🌐 English ⚖ 313 KB

The Influence of n-Alkyl Groups on the R

The Influence of n-Alkyl Groups on the Rate of a Cyclization Reaction

✍ Berliner, Ernst 📂 Article 📅 1944 🏛 American Chemical Society 🌐 English ⚖ 387 KB

Cycloadditions of substituted 1,2-dimeth

Cycloadditions of substituted 1,2-dimethylenecyclopentanes. — The influence of methyl groups on the rate of diels-alder reactions

✍ Sustmann, Reiner ;Daute, Peter ;Sauer, Ralf ;Sommer, Angelika ;Trahanovsky, Walt 📂 Article 📅 1989 🏛 Wiley (John Wiley & Sons) 🌐 English ⚖ 836 KB

The preparation of methyl-substituted 1,2-dimethylenecyclopentanes and their reactivity in (4 + 2) cycloadditions with a,&unsaturated carboxylic esters and nitriles is studied. In kinetic measurements the methyl groups show a moderately rate-enhancing effect. The results are compared with those for

The Simmons—Smith Reaction of trans,tran

The Simmons—Smith Reaction of trans,trans,cis-1,5,9-Cyclododecatriene

✍ Nozaki, Hitosi; Kawanisi, M.; Noyori, Ryôzi 📂 Article 📅 1965 🏛 American Chemical Society 🌐 English ⚖ 294 KB

Influence of the stereochemistry on the

Influence of the stereochemistry on the rate of cyclization of cis and trans-o-hydroxyaryl alkenyl ketones. Mechanistic implications

✍ Miguel A. Miranda; Jaime Primo; Rosa Tormos 📂 Article 📅 1987 🏛 Elsevier Science 🌐 French ⚖ 391 KB

Irradiation of the aryl trans-2-butenoates 4b-e affords the corresponding photmes products lb-e, together with their cis isomers 3b-r. After srparatic:l by means ot' HPLC, the Kin&zs of the basic cyclization of the trans and cis-o-hydroxyketones lb-e and 3b-e to the -chromanones Zb-e were studied. T