Thermal migrations of ally1 groups in linearly-conjugated cyclohexadienones (e.g., eq. 1) (1) proceed readily at temperature6 as low as [email protected] The same reactions, as well as a disconcerting
โฆ LIBER โฆ
Mechanisms of thermal migrations of allyl and benzyl groups in methylenecyclohexadienes
โ Scribed by Bernard Miller; Kwo-Hrong Lai
- Publisher
- Elsevier Science
- Year
- 1971
- Tongue
- French
- Weight
- 196 KB
- Volume
- 12
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
AND BENZYL GROUPS and Kwo-Hrong Lai of Massachusetts, INMETRYLENECYCLGNEKADIES Amherst, Mass. 01002 (Received in USA 29 March 1971; received in UK for publication 5 April 1971) Polyhalomethyl Groups at the quaternary carbons of cross-conjugated methylenecyclohexadienes ("semibenzenes" ia) undergo formal 1,5-shifts to the exocyclic methylene groups when heated to temperatures near 100ยฐ (e.g., _ l?r 2).1 _ A methyl group in semibenzene 2 undergoes a similar l.R = H-Cl -
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