The preparation and absolute configuration of the optically active forms of the diastereoisomers of 2-(1-phenylethyl)amino-1-phenylethanol and their use as chiral auxiliaries in the asymmetric reduction of acetophenone with modified lithium aluminium hydrides-Reference-Cited by-同舟云学术

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The preparation and absolute configuration of the optically active forms of the diastereoisomers of 2-(1-phenylethyl)amino-1-phenylethanol and their use as chiral auxiliaries in the asymmetric reduction of acetophenone with modified lithium aluminium hydrides

Published:1987 Issue: Volume: Page:601
ISSN:0300-922X
Container-title:Journal of the Chemical Society, Perkin Transactions 1
language:en
Short-container-title:J. Chem. Soc., Perkin Trans. 1

Author:

Garry Scott W.,Neilson Douglas G.

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/1987/P1/P19870000601

Cited by 20 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Enantiopurification of Mandelic Acid by Crystallization-Induced Diastereomer Transformation: An Experimental and Computational Study;Crystal Growth & Design;2023-02-20

2. Enantioselective Synthesis of Phenyl-ethanolamines Through Application of Chiral Sulfoxide;Synthetic Communications;2009-08-12

3. Enantioselective addition of dimethylzinc to aldehydes catalyzed by N-substituted mandelamide-Ti(IV) complexes;Tetrahedron: Asymmetry;2005-06

4. Synthesis of unsymmetrical 3,3′-biquinazoline-2,2′-diones by condensation of 3-aminoquinazolinones with benzoxazinones; fortuitous discovery, and further syntheses of 4-H-3-oxo-1,9a,10-triazaanthracen-9-ones;Org. Biomol. Chem.;2005

5. Reductive Aminations of Carbonyl Compounds with Borohydride and Borane Reducing Agents;Organic Reactions;2002-01-09

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