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Paternò–Büchi reaction

The Paternò–Büchi reaction, named after Emanuele Paternò and George Büchi, who established its basic utility and form,[1][2] is a photochemical reaction, specifically a 2+2 photocycloaddition, which forms four-membered oxetane rings from an excited carbonyl and reacting with an alkene.[3]

Paternò–Büchi reaction
Named after Emanuele Paternò
George Büchi
Reaction type Ring forming reaction
Identifiers
Organic Chemistry Portal paterno-buechi-reaction
RSC ontology ID RXNO:0000083
Here an electronically excited carbonyl group is added to a ground state olefin yielding an oxetane.

With substrates benzaldehyde and 2-methyl-2-butene the reaction product is a mixture of structural isomers:

Another substrate set is benzaldehyde and furan[4] or heteroaromatic ketones and fluorinated alkenes.[5]

The alternative strategy for the above reaction is called the Transposed Paternò−Büchi reaction.

See also edit

References edit

  1. ^ Paterno, E.; Chieffi, G. (1909). "Sintesi in chimica organica per mezzo della luce. Nota II. Composti degli idrocarburi non saturi con aldeidi e chetoni" [Synthesis in organic chemistry by means of light. Note II. Compounds of unsaturated hydrocarbons with aldehydes and ketones]. Gazz. Chim. Ital. (in Italian). 39: 341–361.
  2. ^ G. Büchi; Charles G. Inman; E. S. Lipinsky (1954). "Light-catalyzed Organic Reactions. I. The Reaction of Carbonyl Compounds with 2-Methyl-2-butene in the Presence of Ultraviolet Light". Journal of the American Chemical Society. 76 (17): 4327–4331. doi:10.1021/ja01646a024.
  3. ^ Thorsten Bach (1998). "Stereoselective Intermolecular [2 + 2]-Photocycloaddition Reactions and Their Application in Synthesis". Synthesis. 1998 (5): 683–703. doi:10.1055/s-1998-2054. S2CID 196714415.
  4. ^ Thompson, Matthew P.; Agger, Jonathan; Lu Shin Wong (2015). "Paternò–Büchi Reaction as a Demonstration of Chemical Kinetics and Synthetic Photochemistry Using a Light Emitting Diode Apparatus". Journal of Chemical Education. 92 (10): 1716–1720. doi:10.1021/acs.jchemed.5b00129.
  5. ^ Fernandez, Mario Andrés Gomez; Lefebvre, Corentin; Sudau, Alexander; Genix, Pierre; Vors, Jean-Pierre; Abe, Manabu; Hoffmann, Norbert (2021). "Studies on The Application of The Paternò-Büchi Reaction to The Synthesis of Novel Fluorinated Scaffolds". Chemistry – A European Journal. 27 (63): 15722–15729. doi:10.1002/chem.202102621. ISSN 1521-3765. PMID 34523761. S2CID 237514827.

paternò, büchi, reaction, named, after, emanuele, paternò, george, büchi, established, basic, utility, form, photochemical, reaction, specifically, photocycloaddition, which, forms, four, membered, oxetane, rings, from, excited, carbonyl, reacting, with, alken. The Paterno Buchi reaction named after Emanuele Paterno and George Buchi who established its basic utility and form 1 2 is a photochemical reaction specifically a 2 2 photocycloaddition which forms four membered oxetane rings from an excited carbonyl and reacting with an alkene 3 Paterno Buchi reactionNamed after Emanuele Paterno George BuchiReaction type Ring forming reactionIdentifiersOrganic Chemistry Portal paterno buechi reactionRSC ontology ID RXNO 0000083 Here an electronically excited carbonyl group is added to a ground state olefin yielding an oxetane With substrates benzaldehyde and 2 methyl 2 butene the reaction product is a mixture of structural isomers Another substrate set is benzaldehyde and furan 4 or heteroaromatic ketones and fluorinated alkenes 5 The alternative strategy for the above reaction is called the Transposed Paterno Buchi reaction See also editAza Paterno Buchi reaction the aza equivalent of the Paterno Buchi reaction Enone alkene cycloadditions photochemical reaction of an enone with an alkene to give a cyclobutene ring unitReferences edit Paterno E Chieffi G 1909 Sintesi in chimica organica per mezzo della luce Nota II Composti degli idrocarburi non saturi con aldeidi e chetoni Synthesis in organic chemistry by means of light Note II Compounds of unsaturated hydrocarbons with aldehydes and ketones Gazz Chim Ital in Italian 39 341 361 G Buchi Charles G Inman E S Lipinsky 1954 Light catalyzed Organic Reactions I The Reaction of Carbonyl Compounds with 2 Methyl 2 butene in the Presence of Ultraviolet Light Journal of the American Chemical Society 76 17 4327 4331 doi 10 1021 ja01646a024 Thorsten Bach 1998 Stereoselective Intermolecular 2 2 Photocycloaddition Reactions and Their Application in Synthesis Synthesis 1998 5 683 703 doi 10 1055 s 1998 2054 S2CID 196714415 Thompson Matthew P Agger Jonathan Lu Shin Wong 2015 Paterno Buchi Reaction as a Demonstration of Chemical Kinetics and Synthetic Photochemistry Using a Light Emitting Diode Apparatus Journal of Chemical Education 92 10 1716 1720 doi 10 1021 acs jchemed 5b00129 Fernandez Mario Andres Gomez Lefebvre Corentin Sudau Alexander Genix Pierre Vors Jean Pierre Abe Manabu Hoffmann Norbert 2021 Studies on The Application of The Paterno Buchi Reaction to The Synthesis of Novel Fluorinated Scaffolds Chemistry A European Journal 27 63 15722 15729 doi 10 1002 chem 202102621 ISSN 1521 3765 PMID 34523761 S2CID 237514827 Retrieved from https en wikipedia org w index php title Paterno Buchi reaction amp oldid 1173257808, wikipedia, wiki, book, books, library,

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