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Multiple thermal rearrangements. II. Pyrolysis of alkenyl dihydrotropones

โœ Scribed by Cupas, Chris A.; Heyd, William E.; Kong, Ming-Sheng


Book ID
126057086
Publisher
American Chemical Society
Year
1971
Tongue
English
Weight
234 KB
Volume
93
Category
Article
ISSN
0002-7863

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๐Ÿ“œ SIMILAR VOLUMES


Multiple thermal rearrangements. : IV. T
โœ Leonard Hodakowski; Chris A. Cupas ๐Ÿ“‚ Article ๐Ÿ“… 1973 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 162 KB

In previous studies we have shown that the thermal rearrangement of appropriately substituded cycloheptatrienes and dihydrotropones provides a facile synthetic entry to new bridged polycyclic systems. For example, pyrolysis of 7-allyloxycycloheptatriene (lJ produces, in high yield, equal amounts of

Multiple thermal rearrangements. III. Th
โœ C.A. Cupas; M.S. Kong; M. Mullins; W.E. Heyd ๐Ÿ“‚ Article ๐Ÿ“… 1971 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 154 KB

Nechanistic aspects of thermal sigmatropic rearrangements in cycloheptatrienes have been studied extensively.2 In contrast, the synthetic potential of these isomerization reactions has been exploited only recently. For example, a facile entry to tricyclo[4.3.1.03g8]decane (protoadamantane) derivativ

Thermal rearrangement of cyclopropyl and
โœ Wataru Ando ๐Ÿ“‚ Article ๐Ÿ“… 1969 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 143 KB

The thermal rearrangement of cyclopropyl ketones to homoallylic ketones is a efficient process which has recently become well docLmrented(l-3). We nowwishto report the thermal rearrangement of substituted cyclopropyl esters and to supply a new allylic transformation which occurs at higher temperatur

Thermal rearrangements of 1,2-dialkoxybe
โœ Grรถschl, Dieter ;Meier, Herbert ๐Ÿ“‚ Article ๐Ÿ“… 1995 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 133 KB

## Abstract Flash vacuum pyrolysis of 1,2โ€dialkoxybenzenes 1aโ€c leads to the liberation of alkanes from the interacting side chains. A rearrangement of the skeleton yields the __o__โ€hydroxy carbonyl compounds 2 and 4. The generation of phenol 3 can be rationalized by a decarbonylation. The latter r