Chemistry:Carbonyl olefin metathesis

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Carbonyl olefin metathesis is a type of metathesis reaction that entails, formally, the redistribution of fragments of an alkene and a carbonyl by the scission and regeneration of carbon-carbon and carbon-oxygen double bonds respectively. It is a powerful method in organic synthesis using simple carbonyls and olefins and converting them into less accessible products with higher structural complexity.[1]

Photochemical conditions

The carbonyl–olefin metathesis reaction can proceed stepwise under photochemical conditions, where in the first step irradiation by a light source induces a [2+2] cycloaddition between a carbonyl and olefin, known as the Paternò–Büchi reaction. The isolated oxetane intermediate can subsequently be fragmented into a new carbonyl and olefin product under thermal or acidic conditions.[2]

Metal-mediated process

The metal-mediated processes include a carbonyl-olefination and an olefin–olefin metathesis event. There are two general mechanistic schemes to perform this overall transformation: one, reaction of a [M=CHR1] reagent with an alkene to generate a new metal alkylidene, which then couples with a carbonyl group to form the desired substituted alkene and an inactive [M=O] species (type A); two, conversion of the carbonyl moiety into an alkene through Wittig-type alkenylation, followed by metathesis between this newly formed alkene and a second alkene (type B).[3] This transformation could be done in both stepwise (i.e. two-pot) or one-pot fashion.

For Type A transformation, stoichiometric amount of molybdenum or tungsten complex was often used to generate the metal alkylidene intermediate. In Lei's total synthesis of Huperzine Q,[4] they have furnished the cyclopentene ring through carbonyl-olefin metathesis using Schrock molybdenum alkylidene complex. As for Type B transformation, the alkene intermediate was usually formed through treating the carbonyl functional group with reagents like titanocene methylidene, Tebbe, Grubbs, Petasis reagents or in situ generated titanium alkylidenes.[5] Keck and coworkers showcased the utility of in situ generated titanium alkylidene to perform carbonyl-olefin metathesis in their preparation of the C-ring fragment of bryostatin 1[6]

Organocatalyzed process

Hydrazine mediated reactions

In 2012, the Lambert group has reported a ring-opening metathesis of cyclopropenes with aldehydes using a simple hydrazine catalyst through a [3+2]/ retro [3+2] cycloaddition sequence.[7] A detailed mechanism for this metathesis process is described below: the catalytic cycle started with the condensation of aldehyde R1CHO with hydrazine catalyst, and then the reactive intermediate underwent cycloaddition with cyclopropene. After proton transfer, retro-[3+2] took place which gave the desired hydrazonium intermediate. The subsequent hydrolysis liberates the metathesis product and regenerated catalyst. Cyclopropenes worked smoothly but norbornene and stilbene among other olefins did not undergo metathesis with aldehydes under the same conditions.

Lewis acid-mediated reactions

Back in 1971, Demole and co-workers has observed formation of oxetane from olefin and carbonyl through an intramolecular reaction mediated by SnCl4.[8] The authors has proposed a stepwise mechanism. Based on this result, several methods have been developed in intramolecular systems to form the alkene bond through the same oxetane intermediate followed by subsequent formal retro [2+2] reaction thus accomplishing a formal olefin carbonyl ring closing metathesis transformation.[9][10][11] As for intermolecular version, Bickelhaupt and co-workers have observed carbonyl-olefin metathesis product in 15-30% yield from treating benzaldehyde and alkenes upon EPZ-10, a solid Lewis acid.[12] This reaction system was further investigated and improved by Franzén group.[13][14] They found that trityl cation catalyst could promote formal cross metathesis between trisubstituted alkenes and arenecarbaldehydes to give β-alkylstyrene and acetone. The proposed mechanism is shown below.

References

  1. ↑ Becker, Marc R.; Watson, Rebecca B.; Schindler, Corinna S. (2018). "Beyond olefins: new metathesis directions for synthesis". Chemical Society Reviews 47 (21): 7867–7881. doi:10.1039/c8cs00391b. ISSN 0306-0012. PMID 30335106. 
  2. ↑ Mikolajczyk, Marian; Drabowicz, Józef; Omelańczuk, Jan; Fluck, Ekkehard (1975). "Optically active trivalent phosphorus acids esters: an approach by asymmetric synthesis". J. Chem. Soc., Chem. Commun. (10): 382–383. doi:10.1039/c39750000382. ISSN 0022-4936. 
  3. ↑ "1.3.2 Domino Metathesis Reactions Involving Carbonyls" (in en), Applications of Domino Transformations in Organic Synthesis 1 (2016 ed.), Thieme Verlag, 2016, doi:10.1055/sos-sd-219-00088, ISBN 9783131731319 
  4. ↑ Hong, Benke; Li, Houhua; Wu, Jinbao; Zhang, Jing; Lei, Xiaoguang (2015). "Total Syntheses of (−)-Huperzine Q and (+)-Lycopladines B and C" (in en). Angewandte Chemie International Edition 54 (3): 1011–1015. doi:10.1002/anie.201409503. ISSN 1521-3773. PMID 25358669. 
  5. ↑ Rainier, Jon D.; Allwein, Shawn P.; Cox, Jason M. (February 2001). "C-Glycosides to Fused Polycyclic Ethers. A Formal Synthesis of (±)-Hemibrevetoxin B". The Journal of Organic Chemistry 66 (4): 1380–1386. doi:10.1021/jo001514j. ISSN 0022-3263. 
  6. ↑ Keck, Gary E.; Poudel, Yam B.; Cummins, Thomas J.; Rudra, Arnab; Covel, Jonathan A. (February 2011). "Total Synthesis of Bryostatin 1". Journal of the American Chemical Society 133 (4): 744–747. doi:10.1021/ja110198y. ISSN 0002-7863. PMID 21175177. 
  7. ↑ Griffith, Allison K.; Vanos, Christine M.; Lambert, Tristan H. (2012). "Organocatalytic Carbonyl-Olefin Metathesis" (in en). Journal of the American Chemical Society 134 (45): 18581–18584. doi:10.1021/ja309650u. PMID 23126620. 
  8. ↑ "Masthead". Helvetica Chimica Acta 54 (4): fmi. April 1971. doi:10.1002/hlca.19710540401. ISSN 0018-019X. 
  9. ↑ Jackson, Andrew C.; Goldman, Boris E.; Snider, Barry B. (October 1984). "Intramolecular and intermolecular Lewis acid catalyzed ene reactions using ketones as enophiles". The Journal of Organic Chemistry 49 (21): 3988–3994. doi:10.1021/jo00195a022. 
  10. ↑ Schmalz, Hans-Günther; Soicke, Arne; Slavov, Nikolay; Neudörfl, Jörg-Martin (September 2011). "Metal-Free Intramolecular Carbonyl-Olefin Metathesis of ortho-Prenylaryl Ketones". Synlett 2011 (17): 2487–2490. doi:10.1055/s-0030-1260320. ISSN 0936-5214. 
  11. ↑ Ludwig, Jacob R.; Zimmerman, Paul M.; Gianino, Joseph B.; Schindler, Corinna S. (April 2016). "Iron(III)-catalysed carbonyl–olefin metathesis". Nature 533 (7603): 374–379. doi:10.1038/nature17432. ISSN 0028-0836. Bibcode: 2016Natur.533..374L. 
  12. ↑ "New Books(Angew. Chem. Int. Ed. Engl. 19/1994)". Angewandte Chemie International Edition in English 33 (19): 1994. October 1994. doi:10.1002/anie.199419941. 
  13. ↑ Veluru Ramesh Naidu; Bah, Juho; Franzén, Johan (February 2015). "Direct Organocatalytic Oxo-Metathesis, atrans-Selective Carbocation-Catalyzed Olefination of Aldehydes". European Journal of Organic Chemistry 2015 (8): 1834–1839. doi:10.1002/ejoc.201403651. 
  14. ↑ Bhawal, Benjamin N.; Morandi, Bill (2019). "Catalytic Isofunctional Reactions—Expanding the Repertoire of Shuttle and Metathesis Reactions". Angewandte Chemie International Edition 58 (30): 10074–10103. doi:10.1002/anie.201803797. 



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