Journal article

Synthesis and reactivity of a range of 2-ferrocenyl-3-pivaloyl-1,3-oxazolidin-5-ones

Abstract:: A range of novel 2-ferrocenyl-3-pivaloyl-1,3-oxazolidin-5-ones has been synthesised, both with and without 2-substitution on the ferrocenyl moiety in an effort to develop an asymmetric glycine equivalent. While C-4 alkylation of the parent complex 2-ferrocenyl-3-pivaloyl-1,3-oxazolidin-5-one was successful, the presence of a 2-substituent on the ferrocene ring has been found to prevent C-4 enolisation and hence alkylation.

Publication status:: Published

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APA Style

Alonso, F., Davies, S., & Smethurst, C. (1998). Synthesis and reactivity of a range of 2-ferrocenyl-3-pivaloyl-1,3-oxazolidin-5-ones. JOURNAL OF ORGANOMETALLIC CHEMISTRY, 553(1-2), 463–468.

MLA Style

Alonso, F., et al. “Synthesis and Reactivity of a Range of 2-Ferrocenyl-3-Pivaloyl-1,3-Oxazolidin-5-Ones.” JOURNAL OF ORGANOMETALLIC CHEMISTRY, vol. 553, no. 1-2, 1998, pp. 463–68.

Chicago Style

Alonso, F, S Davies, and C Smethurst. 1998. “Synthesis and Reactivity of a Range of 2-Ferrocenyl-3-Pivaloyl-1,3-Oxazolidin-5-Ones.” JOURNAL OF ORGANOMETALLIC CHEMISTRY 553 (1-2): 463–68.
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Publisher copy:: 10.1016/S0022-328X(97)00652-9

Authors

+ Alonso, F More by this author

Role:: Author

+ Davies, S More by this author

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

+ Smethurst, C More by this author

Role:: Author

Journal:: JOURNAL OF ORGANOMETALLIC CHEMISTRY More from this journal
Volume:: 553
Issue:: 1-2
Pages:: 463-468
Publication date:: 1998-02-25
DOI:: 10.1016/S0022-328X(97)00652-9
ISSN:: 0022-328X

Language:: English
Keywords:: planar chirality

oxazolidinone

ferrocenecarboxaldehyde
Pubs id:: pubs:110633
UUID:: uuid:5f425467-811a-4b67-a610-5bdbf18026b4
Local pid:: pubs:110633
Source identifiers:: 110633
Deposit date:: 2012-12-19

Terms of use

Copyright date:: 1998

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

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