1983
DOI: 10.1080/03086648308077764
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Syntheses of Cycloheptatrienes With Sulfur Functional Groups

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Cited by 5 publications
(3 citation statements)
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“…1449 In the synthesis of cycloheptatrienes with sulfur functional groups, Br 2 was used for oxidizing the substrate to the cyclic disulfide. 1450 Imamura et al studied the isomerization of pentane to isopentane over intermetallic compounds (LaAl 2 , CeAl 2 , PrAl 2 , ErAl 2 , SmAl, and ThAl 2 ) oxidized with Br 2 . Increasing Br 2 addition increases the activity of the catalyst, but the selectivity for isopentane decreases.…”
Section: Use Of Molecular Bromine As An Oxidantmentioning
confidence: 99%
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“…1449 In the synthesis of cycloheptatrienes with sulfur functional groups, Br 2 was used for oxidizing the substrate to the cyclic disulfide. 1450 Imamura et al studied the isomerization of pentane to isopentane over intermetallic compounds (LaAl 2 , CeAl 2 , PrAl 2 , ErAl 2 , SmAl, and ThAl 2 ) oxidized with Br 2 . Increasing Br 2 addition increases the activity of the catalyst, but the selectivity for isopentane decreases.…”
Section: Use Of Molecular Bromine As An Oxidantmentioning
confidence: 99%
“…Several dimeric 1,2-bis(2,2′-bipyridinyl)ethane and 1,2-bis(1,10-phenanthrolinyl)ethane ligands have been synthesized in high yields by oxidative coupling of the corresponding monomeric methylene carbanions using Br 2 as the oxidizing agent . In the synthesis of cycloheptatrienes with sulfur functional groups, Br 2 was used for oxidizing the substrate to the cyclic disulfide . Imamura et al studied the isomerization of pentane to isopentane over intermetallic compounds (LaAl 2 , CeAl 2 , PrAl 2 , ErAl 2 , SmAl, and ThAl 2 ) oxidized with Br 2 .…”
Section: Oxidation Reactionsmentioning
confidence: 99%
“…3a, M Zr, R' = H, 63% isolated yield 3b, M = Hf, R'= H, 65% isolated yield 3c, M = Zr, R' = Me, 82% isolated yield (5) Wailes, P. C.; Weigold, H.; Bell, A. P. J. Organomet. Chem.…”
mentioning
confidence: 99%