๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Photochemistry of 2-methylcyclododecanone.

โœ Scribed by David S. Weiss*; Patrick M. Kochanek


Publisher
Elsevier Science
Year
1977
Tongue
French
Weight
250 KB
Volume
18
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

โœฆ Synopsis


The photochemistry of medium ring-cycloalkanones typified by cyclododecan-


๐Ÿ“œ SIMILAR VOLUMES


Photochemistry of 2-cyanofuran
โœ C.J. Samuel; N. Rowlands ๐Ÿ“‚ Article ๐Ÿ“… 1994 ๐Ÿ› Elsevier Science ๐ŸŒ English โš– 291 KB
Photochemistry of 2-methylcycloalkanones
โœ David S. Weiss; Patrick M. Kochanek; James J. Lipka ๐Ÿ“‚ Article ๐Ÿ“… 1977 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 210 KB
Photochemistry of 2-aceto-2-methylmethyl
โœ J.Christopher Dalton; Hak-Foon Chan ๐Ÿ“‚ Article ๐Ÿ“… 1974 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 238 KB

Direct irradiation of B,y-unsaturated ketones with accessible allylic yhydrogens has been reported to yield intramolecular y-hydrogen abstraction,' intramolecular cycloaddition'e and 1,3-acyl shift and a-cleavage processes la,b,f . As part of a study of the effect of stereochemistry on the relative

Photochemistry of Chlorinated 2-Cycloalk
โœ Isabelle Altmeyer; Paul Margaretha ๐Ÿ“‚ Article ๐Ÿ“… 1977 ๐Ÿ› John Wiley and Sons ๐ŸŒ German โš– 400 KB

## Abstract The 6โ€chloroโ€2โ€cyclohexenones **3, 6** and **11**, and the 5โ€chloroโ€2โ€cyclopentenone **15** were newly synthesized. The results obtained with compounds **3** and **15** in photocycloadditions to olefins show that the oxetane __vs.__ cyclobutane product ratio is reduced by the substituti

Photochemistry of 2-(Trifluoromethyl) cy
โœ Christoph Semisch; Paul Margaretha ๐Ÿ“‚ Article ๐Ÿ“… 1984 ๐Ÿ› John Wiley and Sons ๐ŸŒ German โš– 226 KB

## Abstract The photochemical behaviour of the title compound **1a** is compared to that of the nonโ€fluorinated parent ketone 2โ€methylcyclohexanone (**1b**). Substitution of the CH~3~โ€ group on C(2) by a trifluoromethyl group strongly enhances __2H__โ€ and __RH__โ€ reduction product formation in cycl