## Abstract For Abstract see ChemInform Abstract in Full Text.
Reaction of Fluoro-Containing 3-Oxoesters with Benzaldehyde.
β Scribed by M. V. Pryadeina; O. G. Kuzueva; Ya. V. Burgart; V. I. Saloutin
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 32 KB
- Volume
- 33
- Category
- Article
- ISSN
- 0931-7597
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π SIMILAR VOLUMES
Reductive coupling reactions between 4-[ 18 F]fluoro-benzaldehyde ([ 18 F]1) and different alcohols by use of decaborane (B 10 H 14 ) as reducing agent have the potential to synthesize 4-[ 18 F]fluoro-benzylethers in one step. [ 18 F]1 was synthesized from 4trimethylammonium benzaldehyde (triflate s
Benzaldehyde in THF reacts with lithium metal to give the expected reduction product, benzyl alcohol, plus benzoin and benzyl as minor products. The kinetics of the overall reaction as well as the partial rate coefficients of the several steps have been determined under various reaction conditions.
Bbeeimd in USA 26 Jnme 1972; reoeived in DX for pnblioation 21 Angust 1972) We have obtained an unexpected oxidation-reduction product from the reaction of guanidine and benzaldehydes in the presence of strong base. For example, R-cblorobenzaldehyde, guanidine carbonate.and sodium methoxide (3:1:2)