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DOI:
10.1055/sos-SD-133-00326
Kwiatkowska, M.; Kiełbasiński, P., Science of Synthesis Knowledge Updates, (2024) 3, 457.
Dehydrobromination of (E)-1-bromo-3-fluorobut-2-en-2-yl phenyl sulfide (98) and (Z)-1-bromo-3-(bromomethyl)-4,4,4-trifluorobut-2-en-2-yl phenyl sulfide (100) gives rise to 3-fluorobuta-1,3-dien-2-yl phenyl sulfide (99) and phenyl 3-(trifluoromethyl)buta-1,3-dien-2-yl sulfide (101), respectively (Scheme 50).[75]
Meeeee 88 Meeeeeeee ee 8-Meeeeeeeee-8,8-eeee-8-ee Meeeee Meeeeee eee Meeeee 8-(Meeeeeeeeeeeeee)eeee-8,8-eeee-8-ee Meeeeee[88]
| Meeeeeeeee | Meeee (%) | Mee |
|---|---|---|
| e-MeMM, MMM, 88 °M, 8 e | 88 | [88] |
| Me/MM8Me, MeMM, 88 °M, 8 e | 88 | [88] |
References
| [75] | Meee, M.; Meeee, M. M.; Meee, M. M.; Meeee, M. M., Mee. Meee., (8888) 88, 8888. |
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