Stereoselective synthesis of 1,3-disubstituted isoindolines via Rh(iii)-catalyzed tandem oxidative olefination–cyclization of 4-aryl cyclic sulfamidates
Rh(iii)-catalyzed tandem ortho C–H activation/olefination of 4-aryl cyclic sulfamidates and subsequent intramolecular cyclization which lead to the stereoselective synthesis of trans-1,3-disubstituted isoindolines are reported.
1991 ◽
pp. 1263-1265
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1995 ◽
Vol 36
(20)
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pp. 3549-3552
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Keyword(s):
1991 ◽
Vol 32
(27)
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pp. 3205-3208
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Keyword(s):