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Results: 1-3 |
Results: 3
Asymmetric synthesis of beta-amino acids by addition of chiral enolates tonitrones via N-acyloxyimininm ions
Authors: Kawakami, T Ohtake, H Arakawa, H Okachi, T Imada, Y Murahashi, S
Citation: T. Kawakami et al., Asymmetric synthesis of beta-amino acids by addition of chiral enolates tonitrones via N-acyloxyimininm ions, B CHEM S J, 73(11), 2000, pp. 2423-2444
Asymmetric synthesis of beta-amino acids by addition of chiral enolates toN-acyloxyiminium ions and application for synthesis of optically active 5-substituted 8-methylindolizidines
Authors: Kawakami, T Ohtake, H Arakawa, H Okachi, T Imada, Y Murahashi, SI
Citation: T. Kawakami et al., Asymmetric synthesis of beta-amino acids by addition of chiral enolates toN-acyloxyiminium ions and application for synthesis of optically active 5-substituted 8-methylindolizidines, ORG LETT, 1(1), 1999, pp. 107-110
Reversal of diastereoselectivity of the reaction of chiral boron and titanium enolates with nitrones via N-acyloxyiminium intermediates. Asymmetric synthesis of diastereomeric alpha-substituted beta-amino acids
Authors: Kawakami, T Ohtake, H Arakawa, H Okachi, T Imada, Y Murahashi, S
Citation: T. Kawakami et al., Reversal of diastereoselectivity of the reaction of chiral boron and titanium enolates with nitrones via N-acyloxyiminium intermediates. Asymmetric synthesis of diastereomeric alpha-substituted beta-amino acids, CHEM LETT, (8), 1999, pp. 795-796
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