Journal article

CHIRAL RECOGNITION IN THE REACTION OF THE ENOLATE DERIVED FROM [(ETA-5-C5H5)FE(CO)(PPH3)COCH2OCH2PH] WITH CIS-2,3-EPOXYBUTANE AND TRANS-2,3-EPOXYBUTANE - THE STEREOSELECTIVE SYNTHESIS OF CIS AND TRANS-BETA,GAMMA-DISUBSTITUTED-GAMMA-LACTONE

Abstract:: The reaction between the enolate derived from [(η5-C5H5)Fe(CO)(PPh3)CO CH2OCH2Ph] and cis- and trans-2,3-epoxybutane proceeds with a high degree of chiral recognition between the reagents (10:1) to give products which may be converted to β,γ-dimethyl-γ-lactones possessing trans- or cis- stereochemistry. © 1989.

Publication status:: Published

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APA Style

Davies, S., Middlemiss, D., Naylor, A., & Wills, M. (1989). CHIRAL RECOGNITION IN THE REACTION OF THE ENOLATE DERIVED FROM [(ETA-5-C5H5)FE(CO)(PPH3)COCH2OCH2PH] WITH CIS-2,3-EPOXYBUTANE AND TRANS-2,3-EPOXYBUTANE - THE STEREOSELECTIVE SYNTHESIS OF CIS AND TRANS-BETA,GAMMA-DISUBSTITUTED-GAMMA-LACTONE. TETRAHEDRON LETTERS, 30(5), 587–590.

MLA Style

Davies, S, et al. “CHIRAL RECOGNITION IN THE REACTION OF THE ENOLATE DERIVED FROM [(ETA-5-C5H5)FE(CO)(PPH3)COCH2OCH2PH] WITH CIS-2,3-EPOXYBUTANE AND TRANS-2,3-EPOXYBUTANE - THE STEREOSELECTIVE SYNTHESIS OF CIS AND TRANS-BETA,GAMMA-DISUBSTITUTED-GAMMA-LACTONE.” TETRAHEDRON LETTERS, vol. 30, no. 5, 1989, pp. 587–90.

Chicago Style

Davies, S, D Middlemiss, A Naylor, and M Wills. 1989. “CHIRAL RECOGNITION IN THE REACTION OF THE ENOLATE DERIVED FROM [(ETA-5-C5H5)FE(CO)(PPH3)COCH2OCH2PH] WITH CIS-2,3-EPOXYBUTANE AND TRANS-2,3-EPOXYBUTANE - THE STEREOSELECTIVE SYNTHESIS OF CIS AND TRANS-BETA,GAMMA-DISUBSTITUTED-GAMMA-LACTONE.” TETRAHEDRON LETTERS 30 (5): 587–90.
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Publisher copy:: 10.1016/S0040-4039(00)95262-6

Authors

+ Davies, S More by this author

Role:: Author

+ Middlemiss, D More by this author

Role:: Author

+ Naylor, A More by this author

Role:: Author

+ Wills, M More by this author

Role:: Author

Journal:: TETRAHEDRON LETTERS More from this journal
Volume:: 30
Issue:: 5
Pages:: 587-590
Publication date:: 1989-01-01
DOI:: 10.1016/S0040-4039(00)95262-6
ISSN:: 0040-4039

Language:: English
Pubs id:: pubs:168597
UUID:: uuid:0a655165-d9d7-4c9e-a858-e11faf788759
Local pid:: pubs:168597
Source identifiers:: 168597
Deposit date:: 2012-12-19
ARK identifier:: ark:/29072/ora_0a655165d9d74c9ea858e11faf788759

Terms of use

Copyright date:: 1989

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

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