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Caldwell, C.G.6
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MacCoss, M.8
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Cascieri, M.A.16
Carella, A.17
Carver, G.18
Holmes, K.19
Schleif, W.A.20
Danzeisen, R.21
Hazuda, D.22
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Boyd S.A., Matei R.A., Taske A.S., Liu G., Sorensen B.K., Henry K.J., von Geldern T.W., Winn M., Wu-Wong J.R., Chiou W.J., Dixon D.B., Hutchins C.W., Marsh K.C., Nguyen B., Opgenorth T.J. Bioorg. Med. Chem. Lett. 9:1999;1002-1991.
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Von Geldern, T.W.7
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Chiou, W.J.10
Dixon, D.B.11
Hutchins, C.W.12
Marsh, K.C.13
Nguyen, B.14
Opgenorth, T.J.15
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6
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0000629986
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Intermolecular 1,3-dipolar cycloaddition
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For a review on 1,3-dipolar cycloadditions, see: B. Trost. New York: Pergamon. Chapter 4.9
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For a review on 1,3-dipolar cycloadditions, see: Padwa A. Intermolecular 1,3-dipolar cycloaddition. Trost B. Comprehensive Organic Synthesis. 1992;1069-1109 Pergamon, New York. Chapter 4.9.
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Padwa, A.1
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7
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11544346529
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0034975355
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For a review of Rh-catalyzed asymmetric 1,4-additions of organoboronic acids, see:
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For a review of Rh-catalyzed asymmetric 1,4-additions of organoboronic acids, see: Hayashi T. Synlett. 2001;879-887.
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Hayashi, T.1
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12
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0006986415
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Pyrrolines of type
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Pyrrolines of type 5 are readily oxidized to the corresponding pyrrole, see: Shim Y.K., Youn J.I., Chun J.S., Park T.H., Kim M.H., Kim W.J. Synthesis. 1990;753-754.
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Shim, Y.K.1
Youn, J.I.2
Chun, J.S.3
Park, T.H.4
Kim, M.H.5
Kim, W.J.6
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13
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1642633172
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note
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Both 8a and 8c were found to significantly degrade within one week, even with storage at -20 °C under argon.
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17
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1642602101
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note
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3OD): δ 177.91, 140.96, 133.30, 131.50, 130.74, 130.37, 130.00, 128.75, 128.54, 61.10, 59.89, 58.55, 53.49, 48.55 ppm. Results for all NOE experiments can be found in the Supplementary data section.
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