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Synthesis 2005(19): 3219-3224
DOI: 10.1055/s-2005-918486
DOI: 10.1055/s-2005-918486
PAPER
© Georg Thieme Verlag Stuttgart · New York
Synthesis of the C14-C28 Fragment of Tetronasin
Further Information
Received
5 May 2005
Publication Date:
14 November 2005 (online)
Publication History
Publication Date:
14 November 2005 (online)
Abstract
A synthesis of the C14-C28 fragment of Tetronasin features an SE2 reaction between a cationic η3-allylmolybdenum complex and and an α-metallated tetrahydrofuran.
Keywords
π-allyl complex - molybdenum - copper - substitution
- 1
Davies DH.Snape EW.Suter PJ.King TJ.Falshaw CP. J. Chem. Soc., Chem. Commun. 1981, 1073 - 2
Keller-Julsen C.King HD.Kuhn M.Loosli HR.Pache W.Petcher TJ.Weber HP.von Wartburg A. J. Antibiot. 1982, 35: 142 - 3
Newbold CJ.Wallace RJ.Watt ND.Richardson AJ. Appl. Environ. Microbiol. 1988, 54: 544 - 4
Gates RN.Roland LT.Wyatt WE.Hembry FG.Bailie JH. J. Anim. Sci. 1989, 67: 3419 - 5
Hori K.Hikage N.Inagaki A.Mori S.Nomura K.Yoshii E. J. Org. Chem. 1992, 57: 2888 - 6
Hori K.Kazuno H.Nomura K.Yoshii E. Tetrahedron Lett. 1993, 34: 2183 - 7
Hori K.Mori S.Nomura K.Inagaki A.Yoshii E. Chem. Pharm. Bull. 1990, 38: 1784 - 8
Hori K.Nomura K.Kazuno H.Yoshii E. Chem. Pharm. Bull. 1990, 38: 1778 - 9
Ley SV.Clase JA.Mansfield DJ.Osborn HMI. J. Heterocycl. Chem. 1996, 33: 1533 - 10
De Laszlo SE.Ford MJ.Ley SV.Maw GN. Tetrahedron Lett. 1990, 31: 5525 - 11
Ley SV.Brown DS.Clase JA.Fairbanks AJ.Lennon IC.Osborn HMI.Stokes ESE.Wadsworth DJ. J. Chem. Soc., Perkin Trans. 1 1998, 2259 - 12
Ley SV.Wadsworth DJ. Tetrahedron Lett. 1989, 30: 1001 - 13
Ley SV.Trudell ML.Wadsworth DJ. Tetrahedron 1991, 47: 8285 - 14
Semmelhack MF.Kim CR.Dobler W.Meier M. Tetrahedron Lett. 1989, 30: 4925 - 15
Semmelhack MF.Epa WR.Cheung AW.-H.Gu Y.Kim C.Zhang N.Lew W. J. Am. Chem. Soc. 1994, 116: 7455 - 16
Lee HW.Lee IYC.Kim SK. Tetrahedron Lett. 1990, 31: 7637 - 17
Lee HW.Lee IYC. Synlett 1991, 871 - 18
Hill RK.Foley PJ.Gardella LA. J. Org. Chem. 1967, 32: 2330 - 19
Wolinsky J.Chan D. J. Org. Chem. 1965, 30: 41 - 20
Kraus GA.Molina MT. J. Org. Chem. 1988, 53: 752 - 21
Kraus GA.Frazier KA.Roth BD.Taschner MJ.Neuenschwander K. J. Org. Chem. 1981, 46: 2417 - 22
Cooksey J.Gunn A.Kocienski PJ.Kuhl A.Uppal S.Christopher JA.Bell R. Org. Biomol. Chem. 2004, 2: 1719 - 23
Kolb HC.Van Nieuwenhze MS.Sharpless KB. Chem. Rev. 1994, 94: 2483 - 24
Mitsunobu O. Synthesis 1981, 1 - 25
Hughes DL. Org. React. (N.Y.) 1992, 42: 335 - 27
Cohen T.Lin M.-T. J. Am. Chem. Soc. 1984, 106: 1130 - 28
Cohen T.Bhupathy M. Acc. Chem. Res. 1989, 22: 152 - 29
Rychnovsky SD.Plzak K.Pickering D. Tetrahedron Lett. 1994, 35: 6799 - 30
Christopher JA.Kocienski P.Procter M. Synlett 1998, 425 - 31
Freeman PK.Hutchinson LL. J. Org. Chem. 1980, 45: 1924 - 33
Sawyer JS.Kucerovy A.Macdonald TL.McGarvey GJ. J. Am. Chem. Soc. 1988, 110: 842 - 35
Zhao Y.Beddoes RL.Quayle P. Tetrahedron Lett. 1994, 35: 4183 - 36
Amano S.Fujiwara K.Murai A. Chem. Lett. 1998, 409 - 37
Kocienski PJ.Bell R.Bourque E.Christopher JA.Cooksey J.Gunn A.Kuhl A.Li Y.Uppal S.Yuen J. Pure Appl. Chem. 2004, 76: 477 - 38
Faller JW.Linebarrier D. Organometallics 1988, 7: 1670 - 39
Faller JW.Lambert C.Mazzieri MR. J. Organomet. Chem. 1990, 383: 161 - 40 Loss of stereochemical integrity has been observed in the conjugate addition of chiral α-alkoxyalkylcuprates to enones and propiolate esters:
Linderman RJ.Griedel BD. J. Org. Chem. 1990, 55: 5428
References
The five- and six-membered lactones were easily distinguished by their characteristic 13C NMR signals for the C=O groups at δ = 178.1 and 171.2, respectively.
32A pure sample of (23R)-21 could not be obtained; therefore the NOE data was recorded on a mixture enriched in (23R)-21.
34Compound (23R)-27 is an intermediate in the Yoshii synthesis of Tetronomycin (see ref. 5).