Journal article

ASYMMETRIC DIELS-ALDER REACTIONS OF A NITROSO COMPOUND DERIVED FROM D-BORNANE-10,2-SULTAM

Abstract:: Acylnitroso dienophile 3 derived from D-bornane-10,2-sultam undergoes cycloaddition with high yields and complete facial selectivity to cyclopentadiene and cyclohexadiene. When the nitroso group is attached to the sultam nitrogen, it is no longer reactive in Diels-Alder reactions. © 1991.

Publication status:: Published

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APA Style

Gouverneur, V., Dive, G., & Ghosez, L. (1991). ASYMMETRIC DIELS-ALDER REACTIONS OF A NITROSO COMPOUND DERIVED FROM D-BORNANE-10,2-SULTAM. TETRAHEDRON-ASYMMETRY, 2(12), 1173–1176.

MLA Style

Gouverneur, V., et al. “ASYMMETRIC DIELS-ALDER REACTIONS OF A NITROSO COMPOUND DERIVED FROM D-BORNANE-10,2-SULTAM.” TETRAHEDRON-ASYMMETRY, vol. 2, no. 12, 1991, pp. 1173–76.

Chicago Style

Gouverneur, V, G Dive, and L Ghosez. 1991. “ASYMMETRIC DIELS-ALDER REACTIONS OF A NITROSO COMPOUND DERIVED FROM D-BORNANE-10,2-SULTAM.” TETRAHEDRON-ASYMMETRY 2 (12): 1173–76.
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Publisher copy:: 10.1016/S0957-4166(00)80015-4

Authors

+ Gouverneur, V More by this author

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

+ Dive, G More by this author

Role:: Author

+ Ghosez, L More by this author

Role:: Author

Journal:: TETRAHEDRON-ASYMMETRY More from this journal
Volume:: 2
Issue:: 12
Pages:: 1173-1176
Publication date:: 1991-01-01
DOI:: 10.1016/S0957-4166(00)80015-4
EISSN:: 1362-511X
ISSN:: 0957-4166

Keywords:: D-BORNANE-10,2-SULTAM

NITROSO COMPOUNDS

CYCLOADDITION

OXYAMINATION
Pubs id:: pubs:43741
UUID:: uuid:2b4fcee8-0c89-4c7f-a18a-c8ff32f4c234
Local pid:: pubs:43741
Source identifiers:: 43741
Deposit date:: 2012-12-19

Terms of use

Copyright date:: 1991

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

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