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0000302307
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Suzuki, A.5
Miyaura, N.6
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8
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0001644755
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For other room temperature Suzuki conditions on solid support, see Guiles, J. W.; Johnson, S. G.; Murray, W. V. J. Org. Chem. 1996, 61, 5169-5171.
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9
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0015136407
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1H NMR indicates the trans-isomer, tamoxifen, is the major isomer. See Collins, D. J.; Hobbs, J. J.; Emmens, C. W. J. Med. Chem. 1971, 14, 952.
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Emmens, C.W.3
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10
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0025896783
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and references contained within
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For some products with electron rich π-systems, additional isomers are present due to facile isomerization of the double bond. See Murphy, C. S.; Parker, C. J.; McCague, R.; Jordan, V. C. Mol. Pharmacol. 1991, 39, 421 and references contained within.
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11
-
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9844246045
-
-
chemical equation presented
-
chemical equation presented.
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-
-
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15
-
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0013249477
-
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Chenera, B.; Finkelstein, J. A.; Veber, D. F. J. Am. Chem. Soc. 1995, 117, 11999.
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Chenera, B.1
Finkelstein, J.A.2
Veber, D.F.3
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16
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0029865824
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Han, Y.; Walker, S. D.; Young, R. N. Tetrahedron Lett. 1996, 37, 2703.
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Han, Y.1
Walker, S.D.2
Young, R.N.3
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18
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9844240094
-
-
Steamboat Springs, CO, January
-
While this work was in progress, 7 was presented at a conference, but no examples of its application or utility were given: Veber, D. F. Presented at the Second Winter Conference on Medicinal and Bioorganic Chemistry, Steamboat Springs, CO, January 1997.
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Second Winter Conference on Medicinal and Bioorganic Chemistry
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Veber, D.F.1
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19
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9844248699
-
-
note
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The synthesis of 7 is detailed in the Supporting Information.
-
-
-
-
20
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0001646543
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Engler, T. A.; Combrink, K. D.; Ray, J. E. Synth. Commun. 1989, 19, 1735-1744.
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Engler, T.A.1
Combrink, K.D.2
Ray, J.E.3
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