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Thermal aliphatic Claisen rearrangement

F. E. Ziegler, The thermal aliphatic Claisen rearrangement, Chem. Rev. 1988,88, 1423. [Pg.475]

Example 1, Tandem Bamford-Stevens/thermal aliphatic Claisen rearrangement... [Pg.16]

The development of a tandem rhodium-catalyzed Bamford-Stevens/thermal aliphatic Claisen rearrangement sequence was elegantly demonstrated by Stoltz. As a general method to prepare non-carbonyl-stabilized diazo compounds in situ, this group chose to investigate the decomposition of //-aziridinyl imines (also known as Eschenmoser hydrazones) 28. ... [Pg.646]

The aliphatic Claisen Rearrangement is a [3,3]-sigmatropic rearrangement in which an allyl vinyl ether is converted thermally to an unsaturated carbonyl compound. [Pg.74]

The thermal rearrangement of allyl phenyl ethers to o-allyl phenol and its mechanism is very well known to organic chemists. Both the aliphatic and aromatic Claisen rearrangements involve a 3,3-sigmatropic shift. There are reviews providing usefulness of this rearrangement reaction. ... [Pg.113]

See other pages where Thermal aliphatic Claisen rearrangement is mentioned: [Pg.776]    [Pg.641]    [Pg.776]    [Pg.854]    [Pg.560]    [Pg.562]    [Pg.934]    [Pg.497]    [Pg.776]    [Pg.641]    [Pg.776]    [Pg.854]    [Pg.560]    [Pg.562]    [Pg.934]    [Pg.497]    [Pg.854]    [Pg.45]    [Pg.861]    [Pg.582]    [Pg.582]    [Pg.850]    [Pg.861]    [Pg.582]    [Pg.227]    [Pg.424]    [Pg.526]    [Pg.589]    [Pg.94]    [Pg.82]   
See also in sourсe #XX -- [ Pg.16 ]

See also in sourсe #XX -- [ Pg.16 ]

See also in sourсe #XX -- [ Pg.16 ]



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Claisen aliphatic

Claisen aliphatic, thermal

Rearrangement thermal

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