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STEREOSELECTIVE DIELS-ALDER REACTIONS OF A NEW CHIRAL CARBAMOYLNITROSO COMPOUND

Abstract:
A new chiral carbamoylnitroso dienophile 1 has been prepared from a substituted pyrrolidine possessing C2 symmetry. Compound 1 reacts with dienes to yield (4 + 2) cycloadducts with very high diastereoisomeric excesses. © 1990.
Publication status:
Published

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Institution:
University of Oxford
Department:
Oxford, MPLS, Chemistry, Organic Chemistry
Role:
Author
Journal:
TETRAHEDRON-ASYMMETRY
Volume:
1
Issue:
6
Pages:
363-366
Publication date:
1990-01-01
DOI:
EISSN:
1362-511X
ISSN:
0957-4166
URN:
uuid:a5a25e4e-6437-4ee9-b3d3-11be08a4dead
Source identifiers:
43365
Local pid:
pubs:43365
Language:
English

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