Asymmetric synthesis of 3-aryl-substituted 2,3-dihydro-1H-isoindol-1-ones
2001 ◽
Vol 79
(11)
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pp. 1528-1535
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The first asymmetric synthesis of 3-aryl substituted 2,3-dihydro-1H-isoindol-1-ones via a tandem nucleophilic 1,2-addition ring closure procedure from SAMP and (or) RAMP hydrazones and subsequent oxidative cleavage of the auxiliary is reported.Key words: isoindolinones, asymmetric synthesis, hydrazones, 1,2-addition, NN bond cleavage.
2018 ◽
Vol 16
(3)
◽
pp. 583-591
Keyword(s):
2007 ◽
Vol 2007
(22)
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pp. 3707-3710
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