Chemistry:Danishefsky's diene

From HandWiki
Revision as of 13:36, 6 March 2023 by John Stpola (talk | contribs) (url)
(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)
Danishefsky's diene[1]
Structural formula of Danishefsky's diene
Ball-and-stick model of Danishefsky's diene
Names
Preferred IUPAC name
{[(3E)-4-Methoxybuta-1,3-dien-2-yl]oxy}trimethylsilane
Other names
Kitahara diene
trans-1-Methoxy-3-trimethylsilyloxy-buta-1,3-diene
(E)-1-Methoxy-3-trimethylsilyloxy-buta-1,3-diene
Identifiers
3D model (JSmol)
ChemSpider
EC Number
  • 261-753-0
UNII
Properties
C8H16O2Si
Molar mass 172.299 g·mol−1
Density 0.89 g cm−3 (20 °C)[2]
Boiling point 68 to 69 °C (154 to 156 °F; 341 to 342 K) at 0.0189 kPa[2]
Hazards
GHS pictograms GHS02: FlammableGHS07: Harmful
GHS Signal word Warning
H226, H315, H319
P210, P233, P240, P241, P242, P243, P264, P280, P302+352, P303+361+353, P305+351+338, P321, P332+313, P337+313, P362, P370+378, P403+235, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☑Y verify (what is ☑Y☒N ?)
Infobox references
Tracking categories (test):

Danishefsky's diene (Kitahara diene) is an organosilicon compound and a diene with the formal name trans-1-methoxy-3-trimethylsilyloxy-buta-1,3-diene named after Samuel J. Danishefsky.[3][4] Because the diene is very electron-rich it is a very reactive reagent in Diels-Alder reactions. This diene reacts rapidly with electrophilic alkenes, such as maleic anhydride. The methoxy group promotes highly regioselective additions. The diene is known to react with amines,[5] aldehydes, alkenes and alkynes.[4] Reactions with imines [6] and nitro-olefins [7] have been reported.

It was first synthesized by the reaction of trimethylsilyl chloride with 4-methoxy-3-buten-2-one and zinc chloride:[8]

Danishefsky's diene

The diene has two features of interest: the substituents promote regiospecific addition to unsymmetrical dienophiles and the resulting adduct is amenable to further functional group manipulations after the addition reaction. High regioselectivity is obtained with unsymmetrical alkenes with a preference for a 1,2-relation of the ether group with the electron-deficient alkene-carbon. All this is exemplified in this aza Diels-Alder reaction:[9][10]

Danishefsky's diene in Aza-Diels_Alder

In the cycloaddition product, the silyl ether is a synthon for a carbonyl group through the enol. The methoxy group is susceptible to an elimination reaction enabling the formation of a new alkene group.

Applications in asymmetric synthesis have been reported.[11][12][13][14][15][16][17][18][19][20][21][22] Derivatives have been reported.[23]

References

  1. ↑ Sigma-Aldrich product page.
  2. ↑ 2.0 2.1 Sicherheitsdatenblatt Merck.
  3. ↑ Samuel J. Danishefsky; Kitahara, T. Useful diene for the Diels-Alder reaction. J. Am. Chem. Soc. 1974, 96, 7807-7808. doi:10.1021/ja00832a031
  4. ↑ 4.0 4.1 Strategic Applications of Named Reactions in Organic Synthesis, Laszlo Kurti,Barbara Czako, Elsevier 2005
  5. ↑ Acid-Free Aza Diels−Alder Reaction of Danishefsky's Diene with Imines Yu Yuan, Xin Li, and Kuiling Ding: Organic Letters 2002 4 (19), 3309-3311 doi:10.1021/ol0265822
  6. ↑ Alkaline salt-catalyzed aza Diels–Alder reactions of Danishefsky's diene with imines in water under neutral conditions Catherine Loncaric, Kei Manabea and Shū Kobayashi Chem. Commun., 2003, 574-575 doi:10.1039/B300880K
  7. ↑ Exo selective Diels–Alder reaction of nitroolefins with Danishefsky's diene Manabu Node, Kiyoharu Nishide, Hitoshi Imazato, Ryuichi Kurosaki, Takehisa Inoue and Takao Ikariya Chem. Commun., 1996, 2559-2560 doi:10.1039/CC9960002559
  8. ↑ Preparation and Diels-Alder Reaction of a Highly Nucleophilic Diene. Org. Synth., Coll. Vol. 7, p.312 (1990); Vol. 61, p.147 (1983). Link
  9. ↑ Asymmetric aza-Diels-Alder reaction of Danishefsky's diene with imines in a chiral reaction medium Pegot B, Nguyen Van Buu O, Gori D, Vo-Thanh G Beilstein Journal of Organic Chemistry, 2006 Link
  10. ↑ This is an asymmetric reaction with a chiral ionic liquid as chiral solvent. The reported chemical yield is 66% with 60% diastereomeric excess
  11. ↑ Development of an unusually highly enantioselective hetero-Diels-Alder reaction of benzaldehyde with activated dienes catalyzed by hypercoordinating chiral aluminum complexes Simonsen KB1, Svenstrup N, Roberson M, Jorgensen KA. Chemistry. 2000 Jan;6(1):123-8. PMID 10747395
  12. ↑ Catalytic enantioselective aza-Diels-alder reactions of imines--an approach to optically active nonproteinogenic alpha-amino acids Yao S, Saaby S, Hazell RG, Jorgensen KA. Chemistry. 2000 Jul 3;6(13):2435-48. PMID 10939745
  13. ↑ Total syntheses of the Securinega alkaloids (+)-14,15-dihydronorsecurinine, (−)-norsecurinine, and phyllanthine. Han G, LaPorte MG, Folmer JJ, Werner KM, Weinreb SM. J Org Chem. 2000 Oct 6;65(20):6293-306. PMID 11052071
  14. ↑ Racemic and asymmetric Diels-Alder reactions of 1-(2-oxazolidinon-3-yl)-3-siloxy-1,3-butadienes. Janey JM, Iwama T, Kozmin SA, Rawal VH.J Org Chem. 2000 Dec 29;65(26):9059-68.PMID 11149852
  15. ↑ Total asymmetric synthesis of the putative structure of the cytotoxic diterpenoid (−)-sclerophytin a and of the authentic natural sclerophytins A and B. Bernardelli P, Moradei OM, Friedrich D, Yang J, Gallou F, Dyck BP, Doskotch RW, Lange T, Paquette LA. J Am Chem Soc. 2001 Sep 19;123(37):9021-32. doi:10.1021/ja011285y
  16. ↑ A straightforward stereoselective synthesis of D- and L-5-hydroxy-4-hydroxymethyl-2-cyclohexenylguanine. Wang J, Morral J, Hendrix C, Herdewijn P.J Org Chem. 2001 Dec 14;66(25):8478-82. doi:10.1021/jo015924z
  17. ↑ Chiral hetero Diels-Alder products by enantioselective and diastereoselective zirconium catalysis. Scope, limitation, mechanism, and application to the concise synthesis of (+)-Prelactone C and (+)-9-deoxygoniopypyrone. Yamashita Y, Saito S, Ishitani H, Kobayashi S.J Am Chem Soc. 2003 Apr 2;125(13):3793-8. doi:10.1021/ja028186k
  18. ↑ Enantioselective catalysis of hetero Diels-Alder reaction and diethylzinc addition using a single catalyst. Du H, Ding K.Org Lett. 2003 Apr 3;5(7):1091-3. doi:10.1021/ol034143c
  19. ↑ Asymmetric hetero Diels-Alder reactions of Danishefsky's diene and glyoxylate esters catalyzed by chiral bisoxazoline derived catalysts Arun K. Ghosh, Packiarajan Mathivanan, John Cappiello, K. Krishnan Tetrahedron: Asymmetry Volume 7, Issue 8, August 1996, Pages 2165–2168 doi:10.1016/0957-4166(96)00261-3
  20. ↑ Asymmetric Hetero-Diels–Alder Reaction of Danishefsky's Dienes with α-Carbonyl Esters Catalyzed by an Indium(III)–PyBox Complex Bei Zhao and Teck-Peng Loh Organic Letters 2013 15 (12), 2914-2917 doi:10.1021/ol400841s
  21. ↑ A Highly Enantioselective Hetero-Diels−Alder Reaction of Aldehydes with Danishefsky's Diene Catalyzed by Chiral Titanium(IV) 5,5',6,6',7,7',8,8'-Octahydro-1,1'-bi-2-naphthol Complexes Bin Wang, Xiaoming Feng, Yaozong Huang, Hui Liu, Xin Cui and Yaozhong Jiang The Journal of Organic Chemistry 2002 67 (7), 2175-2182 doi:10.1021/jo016240u
  22. ↑ Zheng, J., Lin, L., Fu, K., Zhang, Y., Liu, X. and Feng, X. (2014), Asymmetric Hetero-Diels–Alder Reaction of Danishefsky's Diene with α-Ketoesters and Isatins Catalyzed by a Chiral N,N′-Dioxide/Magnesium(II) Complex. Chem. Eur. J., 20: 14493–14498. doi:10.1002/chem.201404144
  23. ↑ Difluorinated Danishefsky's diene: a versatile C(4) building block for the fluorinated six-membered rings. Amii H, Kobayashi T, Terasawa H, Uneyama K. Org Lett. 2001 Oct 4;3(20):3103-5. doi:10.1021/ol0163631



Retrieved from "https://handwiki.org/wiki/index.php?title=Chemistry:Danishefsky%27s_diene&oldid=2612509"