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Pauson–Khand reaction

From Wikipedia, the free encyclopedia
Chemical reaction

ThePauson–Khand (PK) reaction is achemical reaction, described as a[2+2+1]cycloaddition. In it, analkyne, analkene, andcarbon monoxide combine into a α,β-cyclopentenone in the presence of ametal-carbonyl catalyst[1][2]Ihsan Ullah Khand (1935–1980) discovered the reaction around 1970, while working as a postdoctoral associate withPeter Ludwig Pauson (1925–2013) at theUniversity of Strathclyde in Glasgow.[3][4][5] Pauson and Khand's initial findings were intermolecular in nature, but the reaction has poor selectivity. Some modern applications instead apply the reaction for intramolecular ends.[6]

The traditional reaction requires a stoichiometric amounts ofdicobalt octacarbonyl, stabilized by acarbon monoxideatmosphere.[7] Catalytic metal quantities, enhanced reactivity and yield, orstereoinduction are all possible with the rightchiral auxiliaries, choice oftransition metal (Ti, Mo, W, Fe, Co, Ni, Ru, Rh, Ir and Pd), and additives.[8][9][10][11]

Mechanism

[edit]

While the mechanism has not yet been fully elucidated, Magnus' 1985 explanation[12] is widely accepted for both mono- and dinuclear catalysts, and was corroborated by computational studies published by Nakamura and Yamanaka in 2001.[13] The reaction starts withdicobalt hexacarbonyl acetylene complex. Binding of an alkene gives ametallacyclopentene complex. CO thenmigratorily inserts into an M-C bond.Reductive elimination delivers thecyclopentenone. Typically, the dissociation of carbon monoxide from the organometallic complex is rate limiting.[8]

1:
Alkyne coordination, insertion andligand dissociation to form an18-electron complex;
2:
Ligand dissociation to form a 16-electron complex;
3:
Alkene coordination to form an 18-electron complex;
4:
Alkene insertion and ligand association (synperiplanar, still 18 electrons);
5:
CO migratory insertion;
6, 7:
Reductive elimination of metal (loss of [Co2(CO)6]);
8:
CO association, to regenerate the active organometallic complex.[14]

Selectivity

[edit]

The reaction works with both terminal and internal alkynes, although internal alkynes tend to give lower yields. The order of reactivity for the alkene is

(strained cyclic) > (terminal) > (disubstituted) > (trisubstituted).

Tetrasubstituted alkenes and alkenes with stronglyelectron-withdrawing groups are unsuitable.

With unsymmetrical alkenes or alkynes, the reaction is rarelyregioselective, although some patterns can be observed.

The PK reaction has poor regioselectivity with monosubstituted alkenes.Phenylacetylene and1-octene produce at least 4 isomeric products. ("tol" =toluene)

For mono-substituted alkenes, alkyne substituents typically direct: larger groups prefer the C2 position, and electron-withdrawing groups prefer the C3 position.

An electron-withdrawing group (ethyl benzoatyl) prefers the C3 position. ("Tol" =toluene)

But the alkene itself struggles to discriminate between the C4 and C5 position, unless the C2 position is sterically congested or the alkene has a chelating heteroatom.

The reaction's poor selectivity is ameliorated inintramolecular reactions. For this reason, the intramolecular Pauson-Khand is common in total synthesis, particularly the formation of 5,5- and 6,5-membered fusedbicycles.

An intramolecular Pauson-Khand reaction

Generally, the reaction is highlysyn-selective about the bridgehead hydrogen and substituents on the cyclopentane.

An intramolecular Pauson-Khand reaction produces a bicycle with 97% syn to the bridgehead and 3% anti.

Appropriate chiral ligands or auxiliaries can make the reaction enantioselective (see§ Amine N-oxides).BINAP is commonly employed.

Additives

[edit]
Pauson-Khand in DME (dimethoxyethane? dimethyl ether?) at 120°C

Typical Pauson-Khand conditions are elevated temperatures and pressures in aromatic hydrocarbon (benzene, toluene) or ethereal (tetrahydrofuran, 1,2-dichloroethane) solvents. These harsh conditions may be attenuated with the addition of various additives.

Original reaction: 24 hours at 60°C with 30% yield. Dry reaction: silica, oxygen, 45°C for 0.5 hours for 75% yield.
Adding silica improved this reaction rate by a factor of ≈50.

Absorbent surfaces

[edit]

Adsorbing the metallic complex onto silica or alumina can enhance the rate of decarbonylative ligand exchange as exhibited in the image below.[15][16] This is because the donor posits itself on a solid surface (i.e. silica).[clarification needed] Additionally using a solid support restricts conformational movement (rotamer effect).[17][18][19]

Lewis bases

[edit]

Traditional catalytic aids such as phosphine ligands make the cobalt complex too stable, but bulky phosphite ligands are operable.

Reaction in cyclohexanamine fails to proceed, but with neo-butyl methyl sulfide it runs to 79% yield.

Lewis basic additives, such asn-BuSMe, are also believed to accelerate the decarbonylative ligand exchange process. However, an alternative view holds that the additives make olefin insertion irreversible instead.[20] Sulfur compounds are typically hard to handle and smelly, butn-dodecyl methyl sulfide[21] andtetramethylthiourea[22] do not suffer from those problems and can improve reaction performance.

AmineN-oxides

[edit]

The two most common amineN-oxides areN-methylmorpholineN-oxide (NMO) andtrimethylamineN-oxide (TMANO). It is believed that these additives remove carbon monoxide ligands via nucleophilic attack of theN-oxide onto the CO carbonyl, oxidizing the CO into CO2, and generating an unsaturated organometallic complex.[23][24] This renders the first step of the mechanism irreversible, and allows for more mild conditions.Hydrates of the aforementioned amineN-oxides have similar effect.[25][26][27]

NMO =N‑methylmorpholineN‑oxide, DCM =dichloromethane

N-oxide additives can also improve enantio- and diastereoselectivity, although the mechanism thereby is not clear.[28][29][30]

(NMO =N‑methylmorpholineN‑oxide, DCM =dichloromethane) A step in the total synthesis of epoxydictymene: temperature and ultrasound failed to improve the d.r. for the desired diastereomer (the red hydrogen). But theN-oxide additive, while lower yielding, gave a d.r. of 11:1.[28]

Alternative catalysts

[edit]

(Co)4(CO)12 andCo3(CO)9(μ3-CH) also catalyze the PK reaction[31][32] although Takayamaet al detail a reaction catalyzed bydicobalt octacarbonyl.[33]

The key step in Takayamaet al'sasymmetrictotal synthesis of theLycopodiumalkaloidhuperzine-Q:Co2(CO)8 catalyzes anenyne cyclization.[33] Thesiloxane ring ensures[34] that only a single productenantiomer forms.[33]

One stabilization method is to generate the catalystin situ. Chung reports thatCo(acac)2 can serve as aprecatalyst, activated bysodium borohydride.[35]

Other metals

[edit]

catalyst requires asilver triflate co-catalyst to effect the Pauson–Khand reaction:[36]

PK reaction with Wilkinson's catalyst
PK reaction with Wilkinson's catalyst

Molybdenum hexacarbonyl is a carbon monoxide donor in PK-type reactions betweenallenes andalkynes withdimethyl sulfoxide in toluene.[37] Titanium, nickel,[38] and zirconium[39] complexes admit the reaction. Other metals can also be employed in these transformations.[40][9]

Substrate tolerance

[edit]

In general allenes, support the Pauson–Khand reaction; regioselectivity is determined by the choice of metal catalyst.Density functional investigations show the variation arises from different transition state metal geometries.[41]

PK reaction with molybdenum hexacarbonyl
Molybdenum catalyzes a Pauson-Khand reaction at an allene's internal double bond. Rhodium would catalyze a reaction at this substrate's terminal double-bond instead.

Heteroatoms are also acceptable: Mukaiet al's total synthesis of physostigmine applied the Pauson–Khand reaction to acarbodiimide.[42]

Cyclobutadiene also lends itself to a [2+2+1] cycloaddition, although this reactant is too active to store in bulk. Instead,ceric ammonium nitrate cyclobutadiene is generated in situ fromdecomplexation of stablecyclobutadiene iron tricarbonyl with (CAN).

Pauson Khand reaction Seigal 2005
Pauson Khand reaction Seigal 2005

An example of a newer version is the use of thechlorodicarbonylrhodium(I) dimer, [(CO)2RhCl]2, in the synthesis of(+)-phorbol byPhil Baran. In addition to using a rhodium catalyst, this synthesis features an intramolecular cyclization that results in the normal 5-membered α,β-cyclopentenone as well as 7-membered ring.[43]

Carbon monoxide generationin situ

[edit]

The cyclopentenone motif can be prepared from aldehydes, carboxylic acids, and formates. These examples typically employ rhodium as the catalyst, as it is commonly used indecarbonylation reactions. The decarbonylation and PK reaction occur in the same reaction vessel.[44][45]

See also

[edit]

Further reading

[edit]

For Khand and Pauson's perspective on the reaction:

For a modern perspective:

  • Hartwig, John F. (2010).Organotransition Metal Chemistry: from bonding to catalysis. Mill Valley, Calif.: University Science Books.ISBN 978-1-891389-53-5.OCLC 310401036 – via Knovel.
  • Ríos Torres, Ramón (2012). Rios Torres, Ramon (ed.).The Pauson-Khand reaction: scope, variations, and applications. Hoboken, N.J.: John Wiley & Sons.doi:10.1002/9781119941934.ISBN 978-1-118-30863-9.OCLC 774982574.
  • Gibson, Susan E.; Stevenazzi, Andrea (2003). "The Pauson–Khand Reaction: The Catalytic Age Is Here!".Angew. Chem. Int. Ed.42 (16):1800–1810.doi:10.1002/anie.200200547.PMID 12722067.
  • Buchwald, Stephen L.; Hicks, Frederick A. (1999). "Pauson–Khand-type reactions". In Jacobsen, Eric N.; Pfaltz, Andreas; Yamamoto Hisashi (eds.).Comprehensive Asymmetric Catalysis. Vol. II. Berlin: Springer. pp. 491–513.

References

[edit]
  1. ^Khand, I. U.; Knox, G. R.; Pauson, P. L.; Watts, W. E. (1971). "A cobalt induced cleavage reaction and a new series of arenecobalt carbonyl complexes".Journal of the Chemical Society D: Chemical Communications: 36a.doi:10.1039/C2971000036A.
  2. ^Blanco-Urgoiti, Jaime; Añorbe, Loreto; Pérez-Serrano, Leticia; Domínguez, Gema; Pérez-Castells, Javier (2004). "The Pauson–Khand reaction, a powerful synthetic tool for the synthesis of complex molecules".Chem. Soc. Rev.33 (1):32–42.doi:10.1039/b300976a.PMID 14737507.
  3. ^Werner, Helmut (2014). "Obituary: Peter Ludwig Pauson (1925–2013)".Angew. Chem. Int. Ed.53 (13): 3309.doi:10.1002/anie.201400432.
  4. ^Khand et al. 1973a.
  5. ^Khand et al. 1973b.
  6. ^Schore, N. E.; Croudace, M. C. (1981-12-01). "Preparation of bicyclo[3.3.0]oct-1-en-3-one and bicyclo[4.3.0]non-1(9)-en-8-one via intramolecular cyclization of .alpha.,.omega.-enynes".The Journal of Organic Chemistry.46 (26):5436–5438.doi:10.1021/jo00339a046.ISSN 0022-3263.
  7. ^Buchwald & Hicks 1999.
  8. ^abHartwig 2010.
  9. ^abRíos Torres 2012.
  10. ^Schore, Neil E. (1991). "The Pauson–Khand Cycloaddition Reaction for Synthesis of Cyclopentenones".Org. React.40:1–90.doi:10.1002/0471264180.or040.01.ISBN 0-471-26418-0.
  11. ^Gibson & Stevenazzi 2003.
  12. ^Magnus, Philip; Principe, Lawrence M. (January 1985). "Origins of 1,2- and 1,3-stereoselectivity in dicobaltoctacarbonyl alkene-alkyne cyclizations for the synthesis of substituted bicyclo[3.3.0]octenones".Tetrahedron Letters.26 (40):4851–4854.doi:10.1016/s0040-4039(00)94968-2.ISSN 0040-4039., later expanded toMagnus, Philip; Exon, Christopher; Albaugh-Robertson, Pamela (1985-01-01)."Dicobaltoctacarbonyl-alkyne complexes as intermediates in the synthesis of bicyclo[3.3.0]octenones for the synthesis of coriolin and hirsutic acid".Tetrahedron.41 (24):5861–5869.doi:10.1016/S0040-4020(01)91425-5.ISSN 0040-4020.
  13. ^Yamanaka, Masahiro; Nakamura, Eiichi (2001-02-01). "Density Functional Studies on the Pauson−Khand Reaction".Journal of the American Chemical Society.123 (8):1703–1708.Bibcode:2001JAChS.123.1703Y.doi:10.1021/ja005565+.ISSN 0002-7863.PMID 11456770.
  14. ^Kürti László; Czakó Barbara (2005).Strategic Applications of Named Reactions in Organic Synthesis: background and detailed mechanisms. Amsterdam: Elsevier Academic Press.ISBN 978-0-12-429785-2.OCLC 60792519.
  15. ^Billington, David C.; Willison, Debra (1984). "A simple organocobalt mediated synthesis of substituted 3-oxabicyclo[3.3.0]oct-6-en-7-ones".Tetrahedron Letters.25 (36):4041–4044.doi:10.1016/0040-4039(84)80061-1.ISSN 0040-4039.
  16. ^Morimoto, Takashi; Hirano, Masao; Echigoya, Kohki; Sato, Takafumi (1986). "Oxidation by cobalt(III) acetate. Part 10. Effects of ring substituents on the product distributions in the oxidation of β-methylstyrenes by cobalt(III) acetate in acetic acid".J. Chem. Soc., Perkin Trans. 2 (8):1205–1209.doi:10.1039/p29860001205.ISSN 0300-9580.
  17. ^Brown, Scott W.; Pauson, Peter L. (1990)."The synthesis of nitrogen heterocycles via the intramolecular Khand reaction: formation of tetra- and hexa-hydrocyclopenta[c]pyrrol-5(1H)-ones and hexahydro-6H-2-pyrindin-6-ones".Journal of the Chemical Society, Perkin Transactions 1 (4):1205–1209.doi:10.1039/p19900001205.ISSN 0300-922X.
  18. ^Shilov, Aleksandr E; Shul'pin, Georgiy B (1987-05-31). "Activation and Catalytic Reactions of Alkanes in Solutions of Metal Complexes".Russian Chemical Reviews.56 (5):442–464.Bibcode:1987RuCRv..56..442S.doi:10.1070/rc1987v056n05abeh003282.ISSN 0036-021X.S2CID 250841849.
  19. ^Smit, W.A; Kireev, S.L; Nefedov, O.M; Tarasov, V.A (1989-01-01)."Methylenecyclopropane as an alkene component in the Khand-Pauson reaction".Tetrahedron Letters.30 (30):4021–4024.doi:10.1016/S0040-4039(00)99313-4.ISSN 0040-4039.
  20. ^Valle, Carlos Perez del; Milet, Anne; Gimbert, Yves; Greene, Andrew E. (2005)."Lewis Base Promoters in the Pauson–Khand Reaction: A Different Scenario".Angewandte Chemie International Edition.44 (35):5717–5719.doi:10.1002/anie.200500955.ISSN 1521-3773.PMID 16078280.
  21. ^Cochrane, Alison R.; Kerr, William J.; Paterson, Laura C.; Pearson, Colin M.; Shaw, Paul (2021-01-08)."Advances in the cobalt-catalysed Pauson-Khand reaction: Development of a sulfide-promoted, microwave-assisted protocol".Tetrahedron.78 131805.doi:10.1016/j.tet.2020.131805.ISSN 0040-4020.S2CID 229387356.
  22. ^Reuter, Carin; Vögtle, Fritz (March 2000). "Rotaxanes via Michael Addition†".Organic Letters.2 (5):593–595.doi:10.1021/ol990350u.ISSN 1523-7060.PMID 10814386.
  23. ^Shambayani, Soroosh; Crowe, William E.; Schreiber, Stuart L. (1990-01-01)."N-oxide promoted pauson-khand cyclizations at room temperature".Tetrahedron Letters.31 (37):5289–5292.doi:10.1016/S0040-4039(00)98052-3.ISSN 0040-4039.
  24. ^Alper, Howard; Edward, J. T. (2011-02-03)."Reactions of iron pentacarbonyl with compounds containing the N—O linkage".Canadian Journal of Chemistry.48 (10):1543–1549.doi:10.1139/v70-251.
  25. ^Crawford, James J.; Kerr, William J.; McLaughlin, Mark; Morrison, Angus J.; Pauson, Peter L.; Thurston, Graeme J. (2006-12-04)."Use of a highly effective intramolecular Pauson–Khand cyclisation for the formal total synthesis of (±)-α- and β-cedrene by preparation of cedrone".Tetrahedron.62 (49):11360–11370.doi:10.1016/j.tet.2006.05.044.ISSN 0040-4020.
  26. ^Krafft, Marie E.; Romero, Romulo H.; Scott, Ian L. (1992-09-01). "Pauson-Khand reaction with electron-deficient alkynes".The Journal of Organic Chemistry.57 (20):5277–5278.doi:10.1021/jo00046a001.ISSN 0022-3263.
  27. ^Bernardes, Vania; Kann, Nina; Riera, Antoni; Moyano, Albert; Pericas, Miquel A.; Greene, Andrew E. (1995-10-01). "Asymmetric Pauson-Khand Cyclization: A Formal Total Synthesis of Natural Brefeldin A".The Journal of Organic Chemistry.60 (21):6670–6671.doi:10.1021/jo00126a010.ISSN 0022-3263.
  28. ^abJamison, Timothy F.; Shambayati, Soroosh; Crowe, William E.; Schreiber, Stuart L. (1997-05-01). "Tandem Use of Cobalt-Mediated Reactions to Synthesize (+)-Epoxydictymene, a Diterpene Containing a Trans-Fused 5−5 Ring System".Journal of the American Chemical Society.119 (19):4353–4363.Bibcode:1997JAChS.119.4353J.doi:10.1021/ja970022u.ISSN 0002-7863.
  29. ^Carbery, David R.; Kerr, William J.; Lindsay, David M.; Scott, James S.; Watson, Stephen P. (2000-04-22)."Preparation and reaction of desymmetrised cobalt alkyne complexes".Tetrahedron Letters.41 (17):3235–3239.doi:10.1016/S0040-4039(00)00356-7.ISSN 0040-4039.
  30. ^Jończyk, Andrzej; Konarska, Anna (July 1999)."Generation and Reactions of Ammonium Ylides in Basic Two-Phase Systems: Convenient Synthesis of Cyclopropanes, Oxiranes and Alkenes Substituted with Electron-Withdrawing Groups".Synlett.1999 (7):1085–1087.doi:10.1055/s-1999-2757.ISSN 0936-5214.S2CID 196781210.
  31. ^Kim, Jong Wook; Chung, Young Keun (February 1998). "Pauson-Khand Reaction Catalyzed by Co4(CO)12".Synthesis.1998 (2):142–144.doi:10.1055/s-1998-2016.ISSN 0039-7881.S2CID 196736582.
  32. ^Sugihara, Takumichi; Yamaguchi, Masahiko (1998-10-01). "The Pauson−Khand Reaction Catalyzed by the Methylidynetricobalt Nonacarbonyl Cluster".Journal of the American Chemical Society.120 (41):10782–10783.Bibcode:1998JAChS.12010782S.doi:10.1021/ja982635s.ISSN 0002-7863.
  33. ^abcNakayama, Atsushi; Kogure, Noriyuki; Kitajima, Mariko; Takayama, Hiromitsu (2011). "Asymmetric Total Synthesis of a PentacyclicLycopodium Alkaloid: Huperzine-Q".Angew. Chem. Int. Ed.50 (35):8025–8028.doi:10.1002/anie.201103550.PMID 21751323.S2CID 10947595.
  34. ^Ho, Tse-Lok (2016)."Dicobalt Octacarbonyl".Fiesers' Reagents for Organic Synthesis. Vol. 28.John Wiley & Sons. pp. 251–252.ISBN 978-1-118-94281-9.
  35. ^Lee, Nam Young; Chung, Young Keun (April 1996). "Synthesis of cyclopentenones: The new catalytic cocyclization reaction of alkyne, alkene, and carbon monoxide employing catalytic Co(acac)2 and NaBH4".Tetrahedron Letters.37 (18):3145–3148.doi:10.1016/0040-4039(96)00513-8.ISSN 0040-4039.
  36. ^Nakcheol Jeong, Byung Ki Sung, Jin Sung Kim, Soon Bong Park,Sung Deok Seo, Jin Young Shin, Kyu Yeol In, Yoon Kyung ChoiPauson–Khand-type reaction mediated by Rh(I) catalystsPure Appl. Chem., Vol. 74, No. 1, pp. 85–91,2002. (Online article)
  37. ^Kent, J (1995). "A new allenic Pauson-Khand cycloaddition for the preparation of α-methylene cyclopentenones".Tetrahedron Letters.36 (14):2407–2410.doi:10.1016/0040-4039(95)00315-4.
  38. ^Titanium:Nickel:
    • Zhang, Minghui; Buchwald, Stephen L. (January 1996). "A Nickel(0)-Catalyzed Process for the Transformation of Enynes to Bicyclic Cyclopentenones".The Journal of Organic Chemistry.61 (14):4498–4499.doi:10.1021/jo960410z.ISSN 0022-3263.PMID 11667365.
  39. ^
    • Negishi, Eiichi; Holmes, Steven J.; Tour, James M.; Miller, Joseph A. (1985-04-01). "Metal promoted cyclization. 7. Zirconium-promoted bicyclization of enynes".Journal of the American Chemical Society.107 (8):2568–2569.Bibcode:1985JAChS.107.2568N.doi:10.1021/ja00294a071.ISSN 0002-7863.
    • Negishi, Eiichi; Holmes, Steven J.; Tour, James M.; Miller, Joseph A.; Cederbaum, Fredrik E.; Swanson, Douglas R.; Takahashi, Tamotsu (April 1989). "Metal-promoted cyclization. 19. Novel bicyclization of enynes and diynes promoted by zirconocene derivatives and conversion of zirconabicycles into bicyclic enones via carbonylation".Journal of the American Chemical Society.111 (9):3336–3346.Bibcode:1989JAChS.111.3336N.doi:10.1021/ja00191a035.ISSN 0002-7863.
  40. ^Jeong, Nakcheol; Hwang, Sung Hee; Lee, Youngshin; Chung, Young Keun (April 1994). "Catalytic version of the Intramolecular Pauson-Khand Reaction".Journal of the American Chemical Society.116 (7):3159–3160.Bibcode:1994JAChS.116.3159J.doi:10.1021/ja00086a070.ISSN 0002-7863.
  41. ^Bayden, Alexander S.;Brummond, Kay M.; Jordan, Kenneth D. (2006-10-01)."Computational Insight Concerning Catalytic Decision Points of the Transition Metal Catalyzed [2 + 2 + 1] Cyclocarbonylation Reaction of Allenes".Organometallics.25 (22):5204–5206.doi:10.1021/om0607503.ISSN 0276-7333.PMC 4441411.PMID 26005240.
  42. ^Mukai, Chisato; Yoshida, Tatsunori; Sorimachi, Mao; Odani, Akira (January 2006). "Co2(CO)8-Catalyzed Intramolecular Hetero-Pauson−Khand Reaction of Alkynecarbodiimide: Synthesis of (±)-Physostigmine".Organic Letters.8 (1):83–86.doi:10.1021/ol052562z.ISSN 1523-7060.PMID 16381573.
  43. ^Kawamura, Shuhei; Chu, Hang; Felding, Jakob;Baran, Phil S. (2016)."Nineteen-step total synthesis of (+)-phorbol".Nature.532 (7597):90–93.Bibcode:2016Natur.532...90K.doi:10.1038/nature17153.PMC 4833603.PMID 27007853.
  44. ^Morimoto, Tsumoru; Fuji, Koji; Tsutsumi, Ken; Kakiuchi, Kiyomi (2002). "CO-Transfer Carbonylation Reactions. A Catalytic Pauson−Khand-Type Reaction of Enynes with Aldehydes as a Source of Carbon Monoxide".Journal of the American Chemical Society.124 (15):3806–3807.Bibcode:2002JAChS.124.3806M.doi:10.1021/ja0126881.PMID 11942798.
  45. ^Shibata, Takanori; Toshida, Natsuko; Takagi, Kentaro (2002). "Catalytic Pauson−Khand-Type Reaction Using Aldehydes as a CO Source".Organic Letters.4 (9):1619–1621.doi:10.1021/ol025836g.PMID 11975643.
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