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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
Division:
MPLS
Department:
Chemistry
Sub department:
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
Source identifiers:
43365
Language:
English
Pubs id:
pubs:43365
UUID:
uuid:a5a25e4e-6437-4ee9-b3d3-11be08a4dead
Local pid:
pubs:43365
Deposit date:
2012-12-19

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