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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
Division:
MPLS
Department:
Chemistry
Sub department:
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
Source identifiers:
43741
Keywords:
Pubs id:
pubs:43741
UUID:
uuid:2b4fcee8-0c89-4c7f-a18a-c8ff32f4c234
Local pid:
pubs:43741
Deposit date:
2012-12-19

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