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Terminal alkenes readily undergo cyclization by intramolecular carbolthiation to generated cyclopenylmethyllithiums. Reviews
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18
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70349925443
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Crystallographic data of 10 (CCDC 278769) can be obtained free of charge from the Cambridge Crystallographic Data Center, 12 Union Road, Cambridge CB 1EZ, UK; email: deposit@ccdc.cam.ac.uk.
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Crystallographic data of 10 (CCDC 278769) can be obtained free of charge from the Cambridge Crystallographic Data Center, 12 Union Road, Cambridge CB 1EZ, UK; email: deposit@ccdc.cam.ac.uk.
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19
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21
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70349921142
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Crystallographic data of 21 (CCDC 739965) can be obtained free of charge via from the Cambridge Crystallographic Data Center, 12 Union Road, Cambridge CB 1EZ, UK; email: deposit@ccdc.cam.ac.uk
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Crystallographic data of 21 (CCDC 739965) can be obtained free of charge via from the Cambridge Crystallographic Data Center, 12 Union Road, Cambridge CB 1EZ, UK; email: deposit@ccdc.cam.ac.uk.
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22
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0343016503
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The potassium salts of several phenols were reported to undergo ortho-allylation in the presence of various allylic halides and catalytic amounts of zinc chloride but neither other products nor a mechanism were discussed
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The potassium salts of several phenols were reported to undergo ortho-allylation in the presence of various allylic halides and catalytic amounts of zinc chloride but neither other products nor a mechanism were discussed: Bigi, F.; Casiraghi, G.; Casnati, G.; Sartori, G. Synthesis 1981, 310-312.
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Synthesis
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Bigi, F.1
Casiraghi, G.2
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Sartori, G.4
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23
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0020851963
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However, a 6-member ring transition state can be surmised from a subsequent review by some of the same authors
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However, a 6-member ring transition state can be surmised from a subsequent review by some of the same authors: Casnati, G.; Casiraghi, G.; Pochini, A.; Sartori, G.; Ungaro, R. Pure Appl. Chem. 1983, 55, 1677-1688.
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Casnati, G.1
Casiraghi, G.2
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Ungaro, R.5
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24
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37049106180
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The replacement of the phenylthio group of 23 by allyl, Cl, and F as well as its oxidation to a sulfoxide is recorded in the literature but curiously no synthesis of 23 appears.
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The replacement of the phenylthio group of 23 by allyl, Cl, and F as well as its oxidation to a sulfoxide is recorded in the literature but curiously no synthesis of 23 appears. Nishiyama, H.; Narimatsu, S.; Sakuta, K.; Itoh, K. J. Chem. Soc., Chem. Commun. 1982, 459-460.
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Itoh, K.4
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