N-Sulfonyloxy Carbamates as Reoxidants for the Tethered Aminohydroxylation Reaction-Reference-Cited by-同舟云学术

N-Sulfonyloxy Carbamates as Reoxidants for the Tethered Aminohydroxylation Reaction

Published:2006-02-04 Issue:8 Volume:128 Page:2514-2515
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Donohoe Timothy J.¹,Chughtai Majid J.¹,Klauber David J.¹,Griffin David¹,Campbell Andrew D.¹

Affiliation:

1. Department of Chemistry, Chemistry Research Laboratory, University of Oxford, Mansfield Road, Oxford, OX1 3TA, U.K., Syngenta, Jealott's Hill International Research Centre, Bracknell, Berks, RG42 6EY, U.K., and AstraZeneca Pharmaceuticals, Mereside, Alderley Park, Macclesfield, Cheshire, SK10 4TG, U.K.

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja057389g

Reference12 articles.

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

2. The regioselective aminohydroxylation of allylic carbamates

3. The Tethered Aminohydroxylation (TA) of Cyclic Allylic Carbamates

4. The tethered aminohydroxylation (TA) reactionElectronic supplementary information (ESI) available: Figure: The tethered aminohydroxylation reaction. See http://www.rsc.org/suppdata/ob/b3/b305189g/

5. Efficient Acyclic Stereocontrol Using the Tethered Aminohydroxylation Reaction

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