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Synlett 2009(3): 390-394
DOI: 10.1055/s-0028-1087550
DOI: 10.1055/s-0028-1087550
LETTER
© Georg Thieme Verlag
Stuttgart ˙ New York
Organocatalytic Synthesis of an Alkyltetrahydropyran
Further Information
Received
2 September 2008
Publication Date:
21 January 2009 (online)
Publication History
Publication Date:
21 January 2009 (online)
Abstract
The first synthesis of an alkyltetrahydropyran using a diarylprolinol organocatalyst is described.
Keywords
organocatalysis - tetrahydropyrans - diarylprolinol - cyclization
- Supporting Information for this article is available online:
- Supporting Information
- For reviews on the synthesis of tetrahydropyrans, see:
-
1a
Boivin TLB. Tetrahedron 1987, 43: 3309 -
1b
Elliott MC. J. Chem. Soc., Perkin Trans. 1 2002, 2301 -
1c
Clarke PA.Santos S. Eur. J. Org. Chem. 2006, 2045 -
1d
Tang Y.Oppenheimer J.Song Z.You L.Zhang X.Hsung RP. Tetrahedron 2006, 62: 10785 -
1e
Larrosa I.Romea P.Urpí F. Tetrahedron 2008, 64: 2683 - 2
Lin YY.Risk M.Van Engen D.Clardy J.Golik J.James JC.Nakanishi K. J. Am. Chem. Soc. 1981, 103: 6773 - 3
Murata M.Naoki H.Matsunaga S.Satake M.Yasumoto T. J. Am. Chem. Soc. 1994, 116: 7098 -
4a
Diez D.Marcos IS.Basabe P.Romero RE.Moro RF.Lumeras W.Rodriguez L.Urones JG. Synthesis 2001, 1013 -
4b
Diez D.Nuñez MG.Moro RF.Marcos IS.Basabe P.Urones JG. Synlett 2006, 939 - 5
Gung BW.Francis MB. J. Org. Chem. 1993, 58: 6177 -
6a
Martin VS.Nuñez MT.Ramirez MA.Soler MA. Tetrahedron Lett. 1990, 31: 763 -
6b
Martin VS.Palazon JM. Tetrahedron Lett. 1992, 33: 2399 -
6c
Betancort JM.Martin VS.Padron JM.Palazón JM.Ramirez MA.Soler MA. J. Org. Chem. 1997, 62: 4570 -
6d
Ramirez MA.Padron JM.Palazón JM.Martin VS. J. Org. Chem. 1997, 62: 4584 - 7
Nicolaou KC.Theodorakis EA.Rutjes FPJT.Tienes J.Sato M.Untersteller E.Xiao X.-Y. J. Am. Chem. Soc. 1995, 117: 1171 - 8 For a recent review on the oxa-Michael
reaction, see:
Nising CF.Bräse S. Chem. Soc. Rev. 2008, 37: 1218 -
9a
Enders D.Haertwing A.Raabe G.Runsink J. Eur. J. Org. Chem. 1998, 1771 -
9b
Xong X.Ovens C.Pilling AW.Ward JW.Dixon DJ. Org. Lett. 2008, 10: 565 -
9c
Watanabe H.Machida K.Itoh D.Nagatsuka H.Kitahara T. Chirality 2001, 13: 379 - For reviews on organocatalytic asymmetric conjugate additions, see:
-
10a
Almaºi D.Alonso DA.Nájera C. Tetrahedron: Asymmetry 2007, 18: 299 -
10b
Vicario JL.Badia D.Carrillo L. Synthesis 2007, 2065 - 11
Bertelsen S.Diner P.Johansen RL.Jørgensen KA.
J. Am. Chem. Soc. 2007, 129: 1536 - 12
Kano T.Tanaka Y.Maruoka K. Tetrahedron 2007, 63: 8658 - 13
Li DR.Murugan A.Falck JR. J. Am. Chem. Soc. 2008, 130: 46 -
14a
Govender T.Hojabri L.Moghaddam FM.Arvidsson PI. Tetrahedron: Asymmetry 2006, 17: 1763 -
14b For a review, see:
Shi Y.-L.Shi M. Org. Biomol. Chem. 2007, 5: 1499 -
15a
Rios R.Sundén H.Ibrahem I.Córdova A. Tetrahedron Lett. 2007, 48: 2181 -
15b
Sundén H.Ibrahem I.Zhao G.-L.Eriksson L.Córdova A. Chem. Eur. J. 2007, 13: 574 -
15c See also:
Ibrahem I.Sundén H.Rios R.Zhao G.-L.Córdova A. Chimia 2007, 61: 219 - 16
Li H.Wang J.E-Nunu T.Zu L.Jiang W.Wei S.Wang W. Chem. Commun. 2007, 507 -
17a
Sekino E.Kumamoto T.Tanaka T.Ikeda T.Ishikawa T. J. Org. Chem. 2004, 69: 2760 ; and references cited therein -
17b For a recent guanidine-catalyzed asymmetric
synthesis of 2,2-disubstituted chromane skeletons by intramolecular
oxa-Michael addition, see:
Saito N.Ryoda A.Nakanishi W.Kumamoto T.Ishikawa T. Eur. J. Org. Chem. 2008, 2759 -
18a
Biddle MM.Lin M.Scheidt KA. J. Am. Chem. Soc. 2007, 129: 3830 -
18b See also:
Dittmer C.Raabe G.Hintermann L. Eur. J. Org. Chem. 2007, 5886 - 19
Merschaert A.Delbeke P.Dalozé D.Dive GJ. Tetrahedron Lett. 2004, 45: 4697 - 20
Vidari G.Ferrino S.Grieco PA. J. Am. Chem. Soc. 1984, 106: 3539 - 21
Baldwin JE.Chesworth R.Parker JS.Russel AT. Tetrahedron Lett. 1995, 36: 9551 - 22
Corey EJ.Gillman NW.Ganem BE. J. Am. Chem. Soc. 1968, 90: 5616 - 23
Marco-Contelles JL.de Opazo E.Arroyo N. Tetrahedron 2001, 57: 4729 - 24
Ley SV.Norman J.Griffith WP.Marsden SP. Synthesis 1994, 639 - 25
Van Wyk AW.Davies-Coleman MT. Tetrahedron 2007, 63: 12179 - 26
Marigo M.Franzén J.Poulsen TB.Zhuang W.Jørgensen KA. J. Am. Chem. Soc. 2005, 127: 6964 - 27
Ouellet SG.Tuttle JB.MacMillan DWC. J. Am. Chem. Soc. 2005, 127: 32 - 28
Diez D.Beneitez MT.Marcos IS.Garrido NM.Basabe P.Urones JG. Tetrahedron: Asymmetry 2002, 13: 639 - 31
Katsuki T.Martín VS. Org. React. 1996, 48: 1 - 33
Frisch MJ.Trucks GW.Schlegel HB.Scuseria GE.Robb MA.Cheeseman JR.Montgomery JA.Vreven T.Kudin KN.Burant JC.Millam JM.Iyengar SS.Tomasi J.Barone V.Mennucci B.Cossi M.Scalmani G.Rega N.Petersson GA.Nakatsuji H.Hada M.Ehara M.Toyota K.Fukuda R.Hasegawa J.Ishida M.Nakajima T.Honda Y.Kitao O.Nakai H.Klene M.Li X.Knox JE.Hratchian HP.Cross JB.Bakken V.Adamo C.Jaramillo J.Gomperts R.Stratmann RE.Yazyev O.Austin AJ.Cammi R.Pomelli C.Ochterski JW.Ayala PY.Morokuma K.Voth GA.Salvador P.Dannenberg JJ.Zakrzewski VG.Dapprich S.Daniels AD.Strain MC.Farkas O.Malick DK.Rabuck AD.Raghavachari K.Foresman JB.Ortiz JV.Cui Q.Baboul AG.Clifford S.Cioslowski J.Stefanov BB.Liu G.Liashenko A.Piskorz P.Komaromi I.Martin RL.Fox DJ.Keith T.Al-Laham MA.Peng CY.Nanayakkara A.Challacombe M.Gill PMW.Johnson B.Chen W.Wong MW.Gonzalez C.Pople JA. Gaussian 03, revision B.03 Gaussian, Inc.; Wallingford CT: 2003.
References and Notes
When reductions were performed with NaBH4, MeOH was added as cosolvent.
30A racemic mixture of compound 16 was obtained by iodine cyclization of compound 13 and subsequent NaBH4 reduction of the iodo derivatives obtained.
32See the Supporting Information available.