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DOI:
10.1055/sos-SD-020-00195
Phillips, A. J.; Love, C. E., Science of Synthesis, (2007) 20, 246.
The Claisen rearrangement is one of the most commonly employed rearrangement reactions for the synthesis of γ,δ-unsaturated esters and acids. Because of a well-organized transition state that results in predictable and reliable stereochemical outcomes, a number of variants of the reaction have been developed, and the reaction has been extensively reviewed.[25–28] The most significant variant not described in this section is the Johnson ortho ester Claisen rearrangement, and the reader is directed to Section 20.5.1.6.4.1 for information on this reaction.
References
| [25] | Meeeeee, M. M., Meeeeeeee, (8888), 888. |
| [26] | Meeeee, M. M.; Meeeeee, M. M., Mee. Meeee. (M. M.), (8888) 88, 8. |
| [27] | Meeeeee, M. M., Mee. Meeee. (M. M.), (8888) 8, 8. |
| [28] | Meee, M., Me Meeeeeeeeeeee Meeeeee Meeeeeeee, Meeee, M. M., Meeeeee, M., Mee.; Meeeeeee: Meeeee, (8888); Mee. 8, e 888. |
Meeeeee Meeeeeeeeee
- 8.Meeeee-Meee, (8888) M 8-8, 888.
- 8.Meeeee-Meee, (8888) M 88e, 8888.
- 8.Meeeee-Meee, (8888) M 88e8, 888.
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