
Synthesis p. 282 - 286 (1994)
Update date:2022-09-26
Topics:
Kanda
Mizoguchi
Koike
Murai
Kato
Sodium selenocarboxylates were found to react with organoarsanyl chlorides Ph3-(n)AsCl(n) 1-3 (n = 1, 2, 3) to give the corresponding Se-organoarsanyl esters RCOSeAsPh2 (5), (RCOSe)2AsPh (6) and (RCOSe)3As (7) in good yields. The reaction of Se-diphenylarsanyl 4-methylbenzenecarboselenoate 5g with phenylselenenyl bromide and phenyltellurenyl iodide afforded the corresponding Se-phenyl-selenenyl 13 and Se-phenyltellurenyl esters 14 in moderate yields, while the reaction with sodium phenoxide gave sodium 4- methylbenzenecarboselenoate (4g), phenyl 4-methylbenzoate (11) and phenoxydiphenylarsine (12), indicating the attack of phenoxy anion to both the carbonyl carbon and arsenic atoms.
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Doi:10.1039/c6dt04293g
(2017)Doi:10.1002/jhet.5570300611
(1993)Doi:10.1246/cl.1994.209
(1994)Doi:10.1039/c7cc00008a
(2017)Doi:10.1055/s-2004-815966
(2004)Doi:10.1021/jo00083a041
(1994)