The relanve reactivrtles of ortho-andpara-substituted benzaldehydes wrth the a5butylboron enolate of prnacolone have very dzfferent subsrrtuent dependences ortho subsmmts give large rate enhancements wrth electronreleasmg substituents. wlule para subsntuents gave extremely small rate effects Since c
✦ LIBER ✦
“Large rate accelerations in aldol reaction of ortho-substituted benzaldehydes”
✍ Scribed by G. Das; E.R. Thornton
- Book ID
- 108381950
- Publisher
- Elsevier Science
- Year
- 1992
- Tongue
- French
- Weight
- 32 KB
- Volume
- 33
- Category
- Article
- ISSN
- 0040-4039
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The E/Z ratios of the stilbenes 1 formed in the Wittig reaction of ortho-halo substituted benzyltriphenylphosphonium salts 2 and benzaldehydes 3 were determined. It was found that there is a co-operative effect of one ortho-halo group on each of the two reacting partners which increases Z-selectivit
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