Regioselective electrophilic additions to 2-alkoxy- and 2-alkoxymethyl-7-oxabicyclo[2.2.1]hept-5-ene derivatives

DOI: 10.1016/S0040-4020(01)81476-9

Source and publish data:

Tetrahedron p. 8199 - 8206 (1990)

Update date:2022-07-30

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Authors:

Arjona Arjona

Fernandez De La Pradilla

Pita-Romero

Plumet Plumet

Viso Viso

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Article abstract of DOI:10.1016/S0040-4020(01)81476-9

The influence of the stereochemistry at C-2 on the selectivity of the reaction between PhSeBr and 2-alkoxymethyl substituted oxanorbornenes has been studied. All endo isomers displayed complete regio- and stereocontrol with incorporation of the electrophi

Full text of DOI:10.1016/S0040-4020(01)81476-9

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Product name:5-endo-bromo-6-exo-phenylselenyl-7-oxabicyclo<2.2.1>heptan-2-endo-ol benzyl ether

Cas No:133005-80-8

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