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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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Institution:
University of Oxford
Department:
Oxford, MPLS, Chemistry, Organic Chemistry
Role:
Author
Journal:
TETRAHEDRON-ASYMMETRY
Volume:
2
Issue:
12
Pages:
1173-1176
Publication date:
1991-01-01
DOI:
EISSN:
1362-511X
ISSN:
0957-4166
URN:
uuid:2b4fcee8-0c89-4c7f-a18a-c8ff32f4c234
Source identifiers:
43741
Local pid:
pubs:43741

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