Journal article

The tethered aminohydroxylation (TA) reaction.

Abstract:: Since Sharpless' discovery of the asymmetric aminohydroxylation (AA) reaction, a major challenge for chemists has been to find ways of controlling the regio- and stereochemical outcome of this important reaction. Detailed herein is a review of our novel approach towards gaining reliable and predictable regio- and stereocontrol through the use of a tethered carbamate to promote an intramolecular AA reaction, along with a description of the mechanism proposed for this new methodology.

Publication status:: Published

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APA Style

Donohoe, T., Johnson, P., & Pye, R. (2003). The tethered aminohydroxylation (TA) reaction. Organic and Biomolecular Chemistry, 1(12), 2025–2028.

MLA Style

Donohoe, T., et al. “The Tethered Aminohydroxylation (TA) Reaction.” Organic and Biomolecular Chemistry, vol. 1, no. 12, 2003, pp. 2025–28.

Chicago Style

Donohoe, T, P Johnson, and R Pye. 2003. “The Tethered Aminohydroxylation (TA) Reaction.” Organic and Biomolecular Chemistry 1 (12): 2025–28.
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Publisher copy:: 10.1039/b305189g

Authors

+ Donohoe, T More by this author

Institution:: University of Oxford
Division:: MPLS
Department:: Chemistry
Sub department:: Organic Chemistry
Role:: Author

+ Johnson, P More by this author

Role:: Author

+ Pye, R More by this author

Role:: Author

Journal:: Organic and biomolecular chemistry More from this journal
Volume:: 1
Issue:: 12
Pages:: 2025-2028
Publication date:: 2003-06-01
DOI:: 10.1039/b305189g
EISSN:: 1477-0539
ISSN:: 1477-0520

Language:: English
Pubs id:: pubs:32445
UUID:: uuid:92574b1e-8c4f-428d-9696-5c5169210766
Local pid:: pubs:32445
Source identifiers:: 32445
Deposit date:: 2012-12-19

Terms of use

Copyright date:: 2003

Licence:: Terms and Conditions of Use for Oxford University Research Archive

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