Olson et al., 1976 - Google Patents
Vitamin A synthesis by sulfone alkylation-elimination. C15 halide, C5 hydroxy sulfone approachOlson et al., 1976
- Document ID
- 15402795327072683916
- Author
- Olson G
- Cheung H
- Morgan K
- Neukom C
- Saucy G
- Publication year
- Publication venue
- The Journal of Organic Chemistry
External Links
Snippet
Condensation of l-arylsulfcmyl-2-methyl-4-hydroxy-2-butenes (1) with 1-chloro-and l-bromo- 3-methyl-5-(2, 6, 6-trimethylcyclohexen-l-yl)-penta-2, 4-diene (2) to afford 1-hydroxy-3, 7- dimethyl-4-arylsulfonyl-9-(2, 6, 6-trimethylcyclohexen-l-yl) nona-2, 6, 8-triene (3) and the …
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 OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C 0 title abstract description 32
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