RSS-Feed abonnieren
Bitte kopieren Sie die angezeigte URL und fügen sie dann in Ihren RSS-Reader ein.
https://www.thieme-connect.de/rss/thieme/de/10.1055-s-00000084.xml
Synthesis 2012; 44(18): 2843-2850
DOI: 10.1055/s-0031-1290822
DOI: 10.1055/s-0031-1290822
special topic
Functionalized Cyclopropenes and Methylenecyclopropenes from Dianions of 3-Hydroxymethylcyclopropenes
Weitere Informationen
Publikationsverlauf
Received: 29. Februar 2012
Accepted: 09. März 2012
Publikationsdatum:
08. Mai 2012 (online)
Abstract
1,2-Disubstituted 3-hydroxymethylcyclopropene derivatives have been synthesized by reacting the dianions of 1-alkyl-3-hydroxymethylcyclopropenes with a range of electrophiles. Additionally, a complementary procedure is described for one-pot sequential alkylation/rearrangement to provide a convenient synthesis of a chiral methylenecyclopropane directly from a 1-alkyl-3-hydroxymethylcyclopropene.
Supporting Information
- for this article is available online at http://www.thieme-connect.com/ejournals/toc/synthesis.
- Supporting Information
-
References
-
For reviews, see:
- 1a Miege F, Meyer C, Cossy J. Beilstein J. Org. Chem. 2011; 7: 717
- 1b Marek I, Simaan S, Masarwa A. Angew. Chem. Int. Ed. 2007; 46: 7364
- 1c Rubin M, Rubina M, Gevorgyan V. Chem. Rev. 2007; 107: 3117
- 1d Rubin M, Rubina M, Gevorgyan V. Synthesis 2006; 1221
- 1e Fox JM, Yan N. Curr. Org. Chem. 2005; 9: 719
- 1f Nakamura M, Isobe H, Nakamura E. Chem. Rev. 2003; 103: 1295
- 1g Halton B, Banwell MG In The Chemistry of the Cyclopropyl Group . Patai S, Rappoport Z. Wiley; Chichester: 1987: 1224
- 1h Baird MS. Top. Curr. Chem. 1988; 144: 139
- 1i Baird MS, Schmidt T In Carbocyclic Three-Membered Ring Compounds . de Meijere A. Georg Thieme Verlag; Stuttgart: 1996: 114
- 2a Vincens M, Dumont C, Vidal M, Domnin IN. Tetrahedron 1983; 39: 4281
- 2b D’yakonov IA, Kostikov RR. J. Gen. Chem. USSR (Engl. Transl.) 1964; 34: 1722
- 2c Vincens M, Fadel R, Vidal M. Bull. Soc. Chim. Fr. 1987; 3: 462
- 3a Liao L, Fox JM. J. Am. Chem. Soc. 2002; 124: 14322
- 3b Liu X, Fox JM. J. Am. Chem. Soc. 2006; 128: 5600
- 3c Yan N, Liu X, Fox JM. J. Org. Chem. 2008; 73: 563
- 3d Richey HG. Jr, Bension RM. J. Org. Chem. 1980; 45: 5036
- 3e For carbomagnesation reactions that are directed by allylic hydroxyl substituents, see: Simaan S, Marek I. Org. Lett. 2007; 9: 2569
- 4a Yang Z, Xie X, Fox JM. Angew. Chem. Int. Ed. 2006; 45: 3960
- 4b Xie X, Yang Z, Fox JM. J. Org. Chem. 2010; 75: 3847
- 4c Masarwa A, Stanger A, Marek I. Angew. Chem. Int. Ed. 2007; 46: 8039
- 4d Simaan S, Masarwa A, Bertus P, Marek I. Angew. Chem. Int. Ed. 2006; 45: 3963
- 5a Phan DH. T, Kou KG. M, Dong VM. J. Am. Chem. Soc. 2010; 132: 16354
-
5b Bugaut X, Liu F, Glorius F. J. Am. Chem. Soc. 2011; 133: 8130
- 6 Miege F, Meyer C, Cossy J. Org. Lett. 2010; 12: 248
- 7 Rubina M, Woodward EW, Rubin M. Org. Lett. 2007; 9: 5501
-
Additional reactions of 3-hydroxymethylcyclopropenes include:
- 8a Allylindanation reactions: Araki S, Kenji O, Shiraki F, Hirashita T. Tetrahedron Lett. 2002; 43: 8033
- 8b Carbozincation reactions: Kramer K, Leong P, Lautens M. Org. Lett. 2011; 13: 819
- 9a Doyle MP, Protopova M, Müller P, Ene D, Shapiro EA. J. Am. Chem. Soc. 1994; 116: 8492
- 9b Davies HM. L, Lee GH. Org. Lett. 2004; 6: 1233
- 9c Briones J, Hansen J, Hardcastle K, Autschbach J, Davies HM. L. J. Am. Chem. Soc. 2010; 132: 17211
- 9d Lou Y, Horikawa M, Kloster R, Hawryluk N, Corey EJ. J. Am. Chem. Soc. 2004; 126: 8916
- 9e Goto T, Takeda K, Shimada N, Nambu H, Anada M, Shiro M, Ando K, Hashimoto S. Angew. Chem. Int. Ed. 2011; 50: 6803
- 9f Boruta DT, Dmitrenko O, Yap GP. A, Fox JM. Chem. Sci. 2012; 3: 1589
-
10a Pallerla MK, Fox JM. Org. Lett. 2007; 9: 5625
- 10b Pallerla MK, Fox JM. Org. Lett. 2005; 7: 3593
-
10c Pallerla MK, Yap GP. A, Fox JM. J. Org. Chem. 2008; 73: 6137
- 10d Kireev SL, Smit VA, Ugrak BI, Nefedov OM. Bull. Acad. Sci. USSR, Div. Chem. Sci. (Engl. Transl.) 1991; 40: 2240
- 11a Closs GL, Closs LE. J. Am. Chem. Soc. 1963; 85: 99
- 11b Avezov IB, Bolesov IG, Levina RY. J. Org. Chem. USSR, Div. Chem. Sci. (Engl. Trans.) 1974; 10: 2129
- 11c Isaka M, Matsuzawa S, Yamago S, Ejiri S, Miyachi Y, Nakamura E. J. Org. Chem. 1989; 54: 4727
- 11d Kirms MA, Primke H, Stohlmeier M, de Meijere A. Recl. Trav. Chim. Pays-Bas 1986; 105: 462
- 11e Schipperijn AJ, Smael P. Recl. Trav. Chim. Pays-Bas 1973; 92: 1159
- 12a Zrinski I, Novak-Coumbassa N, Eckert-Maksic M. Organometallics 2004; 23: 2806
- 12b Zrinski I, Eckert-Maksić M. Synth. Commun. 2003; 33: 4071
- 13a Liao L, Yan N, Fox JM. Org. Lett. 2004; 6: 4937
- 13b Fisher LA, Fox JM. J. Org. Chem. 2008; 73: 8474
- 14 Chuprakov S, Rubin M, Gevorgyan V. J. Am. Chem. Soc. 2005; 127: 3714
- 15 Fordyce EA. F, Luebbers T, Lam HW. Org. Lett. 2008; 10: 3993
- 16 Kim R, Sherrill WM, Rubin M. Tetrahedron 2010; 66: 4947
- 17 Audran G, Pellissier H. Adv. Synth. Catal. 2010; 352: 575
-
Formal SN2′, see:
- 18a Nueske H, Bräse S, Meijere A. Synlett 2000; 1467
- 18b Babin D, Pilorge F, Delbarre LM, Demoute JP. Tetrahedron 1995; 51: 9603
- 18c Ref. 4d
- 18d Weatherhead-Kloster RA, Corey EJ. Org. Lett. 2006; 8: 171
- 18e Simaan S, Marek I. Chem. Commun. 2009; 3: 292
- 18f Simaan S, Masarwa A, Zohar E, Stanger A, Marek I, Bertus P. Chem.–Eur. J. 2009; 15: 8449
- 18g Arnaud R, Choubani S, Subra R, Vidal M, Vincens M. Can. J. Chem. 1985; 63: 2512
- 18h Vincens M, Choubani S, Vidal M. Tetrahedron Lett. 1981; 22: 4695
- 18i Ref. 7
- 18j Ref. 4c
- 18k Ref. 18f
- 19a Yamago S, Nakamura M, Wang X, Yanagawa M, Tokumitsu S, Nakamura E. J. Org. Chem. 1998; 63: 1694
- 19b Yamago S, Nakamura E. J. Am. Chem. Soc. 1989; 111: 7285
- 19c Vincens M, Dumont C, Vidal M. Tetrahedron 1981; 37: 2683
- 19d Audo D, Vincens M, Dumont C, Vidal M. Can. J. Chem. 1981; 59: 2199
- 19e Vidal M, Vincens M, Arnaud P. Bull. Soc. Chim. Fr. 1972; 2: 665
- 19f Padwa A, Wannamaker W. Tetrahedron 1991; 32: 6139
- 19g Okazaki R, O-oka M, Akiyama T, Inamoto N, Niwa J, Kato S. J. Am. Chem. Soc. 1987; 109: 5413
- 19h Stierman TJ, Johnson RP. J. Am. Chem. Soc. 1983; 105: 2492
- 19i Formanovskii AA, Leonova LI, Yakushkina NI, Bakhbukh M, Grishin YuK, Bolesov IG. Zh. Org. Khim. 1977; 13: 1883
- 19j Nakamura M, Toganoh M, Wang X, Yamago S, Nakamura E. Chem. Lett. 2000; 6: 664
- 19k Vincens M, Vidal M. Bull. Soc. Chim. Fr. 1985; 5: 900
- 19l Richey H, Wilkins C, Bension R. J. Org. Chem. 1980; 45: 5042
- 19m Warkentin J, Woollard J. Can. J. Chem. 1997; 75: 289
- 19n Vincens M, Dumont C, Vidal M. Bull. Soc. Chim. Fr. 1974; 2811
- 20 Jackman LM, Smith BD. J. Am. Chem. Soc. 1988; 110: 3829
For related work with allylic hydroxy substitutents, see:
Reduction with allylic transposition, see:
For allylic chlorination, see:
For sigmatropic rearrangement, see: