Journal article

Rearrangement of pyrrolines derived from the Birch reduction of electron-deficient pyrroles: Radical ring-expansion to substituted tetrahydropyridines

Abstract:: Access to the synthetically important tetrahydropyridine motif has been achieved by radical rearrangement of pyrrolines obtained from the Birch reduction of electron-deficient pyrroles.

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APA Style

Turner, P., Donohoe, T., & Cousins, R. (2004). Rearrangement of pyrrolines derived from the Birch reduction of electron-deficient pyrroles: Radical ring-expansion to substituted tetrahydropyridines. Chemical Communications, 10(12), 1422–1423.

MLA Style

Turner, P, et al. “Rearrangement of Pyrrolines Derived from the Birch Reduction of Electron-Deficient Pyrroles: Radical Ring-Expansion to Substituted Tetrahydropyridines.” Chemical Communications, vol. 10, no. 12, 2004, pp. 1422–23.

Chicago Style

Turner, P, T Donohoe, and R Cousins. 2004. “Rearrangement of Pyrrolines Derived from the Birch Reduction of Electron-Deficient Pyrroles: Radical Ring-Expansion to Substituted Tetrahydropyridines.” Chemical Communications 10 (12): 1422–23.
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Authors

+ Turner, P More by this author

Role:: Author

+ Donohoe, T More by this author

Role:: Author

+ Cousins, R More by this author

Role:: Author

Journal:: Chemical Communications More from this journal
Volume:: 10
Issue:: 12
Pages:: 1422-1423
Publication date:: 2004-06-21
ISSN:: 1359-7345

Language:: English
Pubs id:: pubs:94430
UUID:: uuid:f4f537c0-14a4-43fa-b3d2-eb72fc046868
Local pid:: pubs:94430
Source identifiers:: 94430
Deposit date:: 2012-12-19
ARK identifier:: ark:/29072/ora_f4f537c014a443fab3d2eb72fc046868

Terms of use

Copyright date:: 2004

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

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