Mislow–Evans rearrangement
The Mislow–Evans rearrangement is a name reaction in organic chemistry. It is named after Kurt Mislow and David A. Evans who discovered this reaction in 1971. The reaction allows the formation of allylic alcohols from allylic sulfoxides in a 2,3-sigmatropic rearrangement.[1]
General reaction scheme[]
The reaction is a powerful way to create particular stereoisomers of the alcohol since it is highly diastereoselective and the chirality at the sulphur atom can be transmitted to the carbon next to the oxygen in the product.
The sulfoxide 1 reagent can be generated easily and enantioselectively from the corresponding sulfide by an oxidation reaction.[2] In this reaction various organic groups can be used, R1 = alkyl, allyl and R2 = alkyl, aryl or benzyl
Mechanism[]
A proposed mechanism is shown below:[2]
The mechanism starts with an allylic sulfoxide 1 which rearranges under heat to a sulfenate ester 2. This can be cleaved using a thiophile, which leaves the allylic alcohol 3 as the product.[3]
Scope[]
The reaction has general application in the preparation of trans-allylic alcohols.[4] Douglass Taber used the Mislow–Evans rearrangement in the synthesis of the hormone Prostaglandin E2.[2]
References[]
- ^ Li, Jie Jack (2006). Name Reaction. Springer. p. 388. doi:10.1007/3-540-30031-7_174. ISBN 978-3-540-30030-4.
- ^ Jump up to: a b c Kürti, László; Czakó, Barbara (2005). Strategic applications of named reactions in Organic Synthesis. Elsevier. p. 292. ISBN 9780124297852.
- ^ Evans, David; Andrews, Glenn (1974). "Allylic sulfoxides. Useful intermediates in organic synthesis". Accounts of Chemical Research. 7 (5): 147–155. doi:10.1021/ar50077a004.
- ^ Zerong Wang (2009), Comprehensive Organic Name Reactions and Reagents (in German), New Jersey: John Wiley & Sons, pp. 1991–1995, ISBN 978-0-471-70450-8
- Name reactions
- Rearrangement reactions