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1
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85031163625
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in press
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For a recent review, see: Magdziak, D.; Toporowski, J.; Meek, S.; Pettus, T. R. R. Curr. Org. Chem., in press.
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Curr. Org. Chem.
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Magdziak, D.1
Toporowski, J.2
Meek, S.3
Pettus, T.R.R.4
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7
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0032577716
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Alcaraz L., Macdonald G., Ragot J.P., Lewis N., Taylor R.J.K. J. Org. Chem. 63:1998;3526-3527.
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Taylor, R.J.K.5
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12
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0000749246
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Solomon M., Jamison W.C.L., McCormick M., Liotta D., Cherry D.A., Mills J.E., Shah R.D., Rodgers J.D., Maryanoff C.A. J. Am. Chem. Soc. 110:1988;3702-3704.
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Solomon, M.1
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Cherry, D.A.5
Mills, J.E.6
Shah, R.D.7
Rodgers, J.D.8
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0038018116
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Schultz A.G., Harrington R.E., Holoboski M.A. J. Org. Chem. 57:1992;2973-2976 Whiting, D. A. In Comprehesive Organic Synthesis; Trost, B. M.; Fleming, I., Eds.; Pergamon Press: Oxford, 1991; Vol. 3, Chapter 3.5, pp. 803-820.
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Schultz, A.G.1
Harrington, R.E.2
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84982065969
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Nishinga, A.1
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Henes, G.5
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0035906496
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Jones R., Van De Water R.W., Lindsey C., Hoarau C., Ung T., Pettus T.R.R. J. Org. Chem. 66:2001;3435-3441.
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Jones, R.1
Van De Water, R.W.2
Lindsey, C.3
Hoarau, C.4
Ung, T.5
Pettus, T.R.R.6
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22
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85031168894
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Additional studies detailing (a) the selection of this particular amide tether, (b) substitiution patterns around the aromatic ring, and (c) enantioselective lactonizations are forthcoming
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Additional studies detailing (a) the selection of this particular amide tether, (b) substitiution patterns around the aromatic ring, and (c) enantioselective lactonizations are forthcoming.
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25
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0010867053
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Jurd L. Tetrahedron. 33:1977;163-168.
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Tetrahedron
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Jurd, L.1
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26
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0028076364
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Angle S.R., Arnaiz D.O., Boyce J.P., Frutos R.P., Louie M.S., Mattson-Arnaiz H.L., Rainier J.D., Turnbull K.D., Yang W. J. Org. Chem. 59:1994;6322-6337.
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Angle, S.R.1
Arnaiz, D.O.2
Boyce, J.P.3
Frutos, R.P.4
Louie, M.S.5
Mattson-Arnaiz, H.L.6
Rainier, J.D.7
Turnbull, K.D.8
Yang, W.9
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29
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85031166311
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6 was found to be the minor product, formed in a 1:2 ratio with a cyclohexadienone which we were unable to isolate. However, due to the relatively high yield of 6, we believe the cylcohexadienone to be compound which can undergo a [3,3]-sigmatropic rearrangement and tautomerization thereby producing 6 upon chromatography.
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6 was found to be the minor product, formed in a 1:2 ratio with a cyclohexadienone which we were unable to isolate. However, due to the relatively high yield of 6, we believe the cylcohexadienone to be compound i which can undergo a [3,3]-sigmatropic rearrangement and tautomerization thereby producing 6 upon chromatography.
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31
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0001096403
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Kita Y., Takada T., Ibaraki M., Gyoten M., Mihara S., Fujita S., Tohma H. J. Org. Chem. 61:1996;223-227.
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(1996)
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Kita, Y.1
Takada, T.2
Ibaraki, M.3
Gyoten, M.4
Mihara, S.5
Fujita, S.6
Tohma, H.7
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32
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0000247985
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Kita Y., Arisawa M., Gyoten M., Nakajima M., Hamada R., Tohma H., Takada T. J. Org. Chem. 63:1998;6623-6625.
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(1998)
J. Org. Chem.
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Kita, Y.1
Arisawa, M.2
Gyoten, M.3
Nakajima, M.4
Hamada, R.5
Tohma, H.6
Takada, T.7
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33
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85031167721
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1H NMR spectra with only trace amounts of the alcohol 14 present. However, upon chromatography significant amounts of 14 are isolated.
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1H NMR spectra with only trace amounts of the alcohol 14 present. However, upon chromatography significant amounts of 14 are isolated.
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35
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85031169179
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note
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abstract
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