Mislow–Evans rearrangement

The Mislow–Evans rearrangement is a name reaction in organic chemistry. It is named after Kurt Mislow who reported the prototypical reaction in 1966,[1] and David A. Evans who published further developments.[2] The reaction allows the formation of allylic alcohols from allylic sulfoxides in a 2,3-sigmatropic rearrangement.[3]

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.

Mislow-Evans-ÜbersichtsreaktionV2

The sulfoxide 1 reagent can be generated easily and enantioselectively from the corresponding sulfide by an oxidation reaction.[4] 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:[4]

Reaktionsmechanismus Mislow-Evans-Umlagerung

The mechanism starts with an allylic sulfoxide 1 which undergoes a thermal 2,3-sigmatropic rearrangement to give a sulfenate ester 2. This can be cleaved using a thiophile, such as phosphite ester, which leaves the allylic alcohol 3 as the product.[5]

Scope

The reaction has general application in the preparation of trans-allylic alcohols.[6] Douglass Taber used the Mislow–Evans rearrangement in the synthesis of the hormone prostaglandin E2.[4]

References

Mislow, Kurt (1966). "Mechanisms of Thermal Racemization of Sulfoxides". Journal of the American Chemical Society. 88 (13): 3138–3139. doi:10.1021/ja00965a048.
Evans, David A. (1971). "Reversible 1,3 transposition of sulfoxide and alcohol functions. Potential synthetic utility". Journal of the American Chemical Society. 93 (19): 4956–4957. doi:10.1021/ja00748a075.
Li, Jie Jack (2006). Name Reaction. Springer Publishing. p. 388. doi:10.1007/3-540-30031-7_174. ISBN 978-3-540-30030-4.
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

This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.

[1] Mislow, Kurt (1966). "Mechanisms of Thermal Racemization of Sulfoxides". Journal of the American Chemical Society. 88 (13): 3138–3139. doi:10.1021/ja00965a048.

[2] Evans, David A. (1971). "Reversible 1,3 transposition of sulfoxide and alcohol functions. Potential synthetic utility". Journal of the American Chemical Society. 93 (19): 4956–4957. doi:10.1021/ja00748a075.

[3] Li, Jie Jack (2006). Name Reaction. Springer Publishing. p. 388. doi:10.1007/3-540-30031-7_174. ISBN 978-3-540-30030-4.

[Kürti-4] Kürti, László; Czakó, Barbara (2005). Strategic applications of named reactions in Organic Synthesis. Elsevier. p. 292. ISBN 9780124297852.

[5] Evans, David; Andrews, Glenn (1974). "Allylic sulfoxides. Useful intermediates in organic synthesis". Accounts of Chemical Research. 7 (5): 147–155. doi:10.1021/ar50077a004.

[Wang-6] 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