Journal article

N-acyl-5,5-dimethyl-oxazolidin-2-ones as latent aldehyde equivalents

Abstract:: N-acyl-5,5-dimethyl-oxazolidin-2-ones can function as versatile latent aldehyde equivalents - reductive cleavage with DIBAL-H affords aldehydes in good yield, while tandem DIBAL-H/Wittig methodology affords α,β-unsaturated esters.

Publication status:: Published

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APA Style

Bach, J., Bull, S., Davies, S., Nicholson, R., Sanganee, H., & Smith, A. (1999). N-acyl-5,5-dimethyl-oxazolidin-2-ones as latent aldehyde equivalents. TETRAHEDRON LETTERS, 40(36), 6677–6680.

MLA Style

Bach, J., et al. “N-Acyl-5,5-Dimethyl-Oxazolidin-2-Ones as Latent Aldehyde Equivalents.” TETRAHEDRON LETTERS, vol. 40, no. 36, 1999, pp. 6677–80.

Chicago Style

Bach, J, S Bull, S Davies, R Nicholson, H Sanganee, and A Smith. 1999. “N-Acyl-5,5-Dimethyl-Oxazolidin-2-Ones as Latent Aldehyde Equivalents.” TETRAHEDRON LETTERS 40 (36): 6677–80.
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Publisher copy:: 10.1016/S0040-4039(99)01345-3

Authors

+ Bach, J More by this author

Role:: Author

+ Bull, S 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

+ Nicholson, R More by this author

Role:: Author

+ Sanganee, H More by this author

Role:: Author

More authors...

Journal:: TETRAHEDRON LETTERS More from this journal
Volume:: 40
Issue:: 36
Pages:: 6677-6680
Publication date:: 1999-09-03
DOI:: 10.1016/S0040-4039(99)01345-3
ISSN:: 0040-4039

Language:: English
Pubs id:: pubs:110616
UUID:: uuid:dd964225-4689-4f55-81c8-95e240a1572f
Local pid:: pubs:110616
Source identifiers:: 110616
Deposit date:: 2012-12-19

Terms of use

Copyright date:: 1999

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

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