Reactions of (9-Anthryl)arylmethyl Chloride and Its Homologues with Nucleophiles under Solvolytic Conditions. Notable Effects of Reaction Conditions and Substituents on the Reaction Sites

DOI: 10.1021/ja00395a025

Source and publish data:

Journal of the American Chemical Society p. 1145 - 1153 (1981)

Update date:2022-08-03

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Authors:

Ogata, Fujimaro

Takagi, Masato

Nojima, Masatomo

Kusabayashi, Shigekazu

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Article abstract of DOI:10.1021/ja00395a025

The reactions of (9-anthryl)arylmethyl chlorides 2a-e (the substituents are p-MeO, p-Me, H, p-Cl, and m-Cl), the corresponding bromides 3b-d (the substituents are p-Me, H, and p-Cl), and the antimonate salts 4b-e (the substituents are p-Me, H, p-Cl, and m

Full text of DOI:10.1021/ja00395a025

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