Long-range proton-proton coupling constants between the aldehyde proton and the ring protons were used to deduce the confonnational preference of 1-naphthaldehyde, 2-naphthaldehyde, 2-hydroxy-1-naphthaldehyde, 2-methoxy-1-naphthaldehyde and 1-bromo-2-naphthaldehyde. Molecular orbital calculations at
Conformational preference of substituted naphthalenes 3—derivatives of methoxy- and acetyl-naphthalene
✍ Scribed by Salman R. Salman
- Publisher
- John Wiley and Sons
- Year
- 1985
- Tongue
- English
- Weight
- 269 KB
- Volume
- 23
- Category
- Article
- ISSN
- 0749-1581
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📜 SIMILAR VOLUMES
Long-range proton-proton coupling constants between the hydroxy proton and ring protons were employed to deduce the confomtional preferences of 1-and 2-hydroxynaphthalene. 2,6-Dibromo-1,5-dihydroxynaphthalene, 2-acetyl-l-hydroxynaphthalene, 1,6-dibromo-2-hydroxynaphthalene and 2-hydroxy-1-naphthalde
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## Abstract The reaction of tetrakis(thf)lithium dimesityl‐1,8‐naphthalenediylborate with either Ph~2~ SbCl or Ph~2~BiCl afforded 1‐(diphenylantimony)‐8‐(dimesitylboron)naphthalenediyl (**1**) and 1‐(diphenylbismuth)‐8‐(dimesitylboron) naphthalenediyl (**2**). These unprecedented boron/antimony and
Naphthalene-Catalyzed Lithiation of N,N-Diisopropylbenzamide and Its Methoxy Derivatives. -The title reaction of benzamides (I) and (IV) leads to the corresponding dihydro derivatives whereas methoxybenzamides (VI) and (IX) react via reductive demethoxylation to give the substituted benzamides (VIII