NUCLEOPHILIC REACTIONS OF FLUOROOLEFINS. II. REGIOSELECTIVITY AND ELIMINATION-ADDITION COMPETITION IN THE REACTION OF 1-PHENYLPENTAFLUOROPROPENES WITH SODIUM ETHOXIDE

DOI: 10.1016/S0022-1139(00)81242-7

Source and publish data:

Journal of Fluorine Chemistry p. 201 - 220 (1982)

Update date:2022-08-30

Topics:: Authors:

Dmowski, Wojciech

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Article abstract of DOI:10.1016/S0022-1139(00)81242-7

1-Phenylpentafluoropropene and its para-substituted analogs 1 are susceptible to nucleophilic attack at both vinylic carbon atoms C-1 and C-2.They react with ethanolic sodium ethoxide to give predominantly substitution products, 1-ethoxy-1-phenyltetrafluo

Full text of DOI:10.1016/S0022-1139(00)81242-7

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NUCLEOPHILIC REACTIONS OF FLUOROOLEFINS. II. REGIOSELECTIVITY AND ELIMINATION-ADDITION COMPETITION IN THE REACTION OF 1-PHENYLPENTAFLUOROPROPENES WITH SODIUM ETHOXIDE

DOI: 10.1016/S0022-1139(00)81242-7

Source and publish data:

Authors:

Article abstract of DOI:10.1016/S0022-1139(00)81242-7

Full text of DOI:10.1016/S0022-1139(00)81242-7

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