- 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
- Publisher copy:
- 10.1016/0957-4166(90)90034-8
-
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- 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
- Copyright date:
- 1990
Journal article
STEREOSELECTIVE DIELS-ALDER REACTIONS OF A NEW CHIRAL CARBAMOYLNITROSO COMPOUND
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