Publication | Closed Access
Model Reactions for the Stereo‐Controlled Synthesis of Aminopolyols; Reduction of Isoxazolines with Free or Protected Hydroxy Groups in Position 4 or in Side Chains
70
Citations
12
References
1981
Year
Hydride AdditionsEngineeringOrganic ChemistryHeterocycle ChemistryChemical DerivativeIsoxazoline DerivativesAmino SugarsStereo‐controlled SynthesisStereoselective SynthesisModel ReactionsBiochemistryDiversity-oriented SynthesisPharmacologyEnantioselective SynthesisBiomolecular EngineeringNatural SciencesSide ChainsDerivative (Chemistry)Synthetic Chemistry
The effects of substituents on asymmetric induction in hydride additions have been investigated on isoxazoline derivatives; the results, which are of importance for the synthesis of hydroxylated amino acids, sphingolipid bases or amino sugars, can be rationalized with the models (1) and (2).
| Year | Citations | |
|---|---|---|
1977 | 525 | |
1980 | 506 | |
1978 | 207 | |
1977 | 122 | |
1974 | 71 | |
1979 | 60 | |
1980 | 59 | |
1981 | 47 | |
1973 | 44 | |
Effects of Neighboring Functional Groups in the Asymmetric Reduction of ω-Substituted Alkyl Phenyl Ketones with Lithium Tri-<i>l</i>-Menthoxyaluminum Hydride Shozo Yamaguchi, Kuninobu Kabuto Bulletin of the Chemical Society of Japan Chemical EngineeringEngineeringAlkene MetathesisResulting AlcoholsLanthanideinduced Shifts | 1977 | 32 |
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