Efficient Acyclic Stereocontrol Using the Tethered Aminohydroxylation Reaction-Reference-Cited by-同舟云学术

Efficient Acyclic Stereocontrol Using the Tethered Aminohydroxylation Reaction

Published:2004-07-01 Issue:15 Volume:6 Page:2583-2585
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Donohoe Timothy J.¹,Johnson Peter D.¹,Pye Richard J.¹,Keenan Martine¹

Affiliation:

1. Department of Chemistry, University of Oxford, Chemistry Research Laboratory, Mansfield Road, Oxford OX1 3TA, U.K., and Eli Lilly and Company, Ltd., Lilly Research Centre, Erl Wood Manor, Sunninghill Road, Windlesham, Surrey GU20 6PH, U.K.

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol049136i

Reference10 articles.

1. The Synthesis of Vicinal Amino Alcohols

2. N-Halocarbamate Salts Lead to More Efficient Catalytic Asymmetric Aminohydroxylation

3. Asymmetric amino-hydroxylation of dienylsilanes. An efficient route to amino-cyclitols

4. A Substrate-Based Methodology That Allows the Regioselective Control of the Catalytic Aminohydroxylation Reaction

5. Reversal of Regioselection in the Sharpless Asymmetric Aminohydroxylation of Aryl Ester Substrates

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