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11
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58149290207
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The diene reduction using PhSeH may proceed via (i) the addition of the selenol to diene to form allylic selenide;
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The diene reduction using PhSeH may proceed via (i) the addition of the selenol to diene to form allylic selenide;
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12
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58149300208
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the generation of allylic radical from allylic selenide upon photo-irradiation or by the attack of seleno radical;
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(ii) the generation of allylic radical from allylic selenide upon photo-irradiation or by the attack of seleno radical;
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13
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0001459562
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14
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33947480236
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For the synthesis of 2,3-dimethyl-2-butenyl phenyl sulfide 3a, see for example
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For the synthesis of 2,3-dimethyl-2-butenyl phenyl sulfide (3a), see for example: A. A. Oswald, K. Griesbaum, W. A. Thaler, B. E. Hudson, Jr., J. Am. Chem. Soc. 1962, 84, 3897.
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33845183210
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-l. See for example: J. A. Franz, B. A. Bushaw, M. S. Alnajjar, J. Am. Chem. Soc. 1989, 111, 268.
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-l. See for example: J. A. Franz, B. A. Bushaw, M. S. Alnajjar, J. Am. Chem. Soc. 1989, 111, 268.
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17
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0001086740
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-1, respectively. See for example: a) G. A. Russell, H. Tashtoush, J. Am. Chem. Soc. 1983, 105, 1398.
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-1, respectively. See for example: a) G. A. Russell, H. Tashtoush, J. Am. Chem. Soc. 1983, 105, 1398.
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19
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0000588714
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c) G. A. Russell, P. Ngoviwatchai, H. I. Tashtoush, A. Pla-Dalmau, R. K. Khanna, J. Am. Chem. Soc. 1988, 110, 3530.
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20
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58149286552
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2 successfully afforded the thioselenated dienes without the formation of any polymerization products (see: Ref. 2b).
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2 successfully afforded the thioselenated dienes without the formation of any polymerization products (see: Ref. 2b).
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