Synthesis of 10-Methyl-δ4-octalins by Diels-Alder Reactions of 2H-Thiopyran Surrogates for 1-Ethenyl-2-methylcyclohexene. -In view of the interest in Diels-Alder reactions of 1-ethenyl-2-methylcyclohexene derivatives as a route to natural product skeletons, the use of the 2H-thiopyran diene surroga
Synthesis of 10-methyl-Δ4-octalins by Diels–Alder reactions of 2H-thiopyran surrogates for 1-ethenyl-2-methylcyclohexene
✍ Scribed by Ward, Dale E.; Gai, Yuanzhu
- Book ID
- 111900595
- Publisher
- NRC Research Press
- Year
- 1997
- Tongue
- French
- Weight
- 286 KB
- Volume
- 75
- Category
- Article
- ISSN
- 0008-4042
- DOI
- 10.1139/v97-082
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📜 SIMILAR VOLUMES
The title compound can be obtained with up to five asymmetric centres of known absolute configuration by a diastereoselective intramolecular Diels-Alder reaction between optically active N-substituted fuffurylamines and maleic anhydride, in which the chirality is transferred from one stereocentre to
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