HIGHLY STEREOSELECTIVE SYNTHESIS OF DI- AND TRISUBSTITUTED HOMOALLYLIC ALCOHOLS VIA PALLADIUM(O)-CATALYZED NUCLEOPHILIC OPENING OF VINYLIC OXETANES

DOI: 10.1016/S0040-4039(00)99420-6

Source and publish data:

Tetrahedron Letters p. 3487 - 3490 (1989)

Update date:2022-08-02

Topics:

Authors:

Larock, Richard C.

Stolz-Dunn, Sandra K.

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Article abstract of DOI:10.1016/S0040-4039(00)99420-6

Vinylic oxetanes react in an S_N2' manner with a variety of potential nucleophiles in the presence of catalytic amounts of Pd(PPh3)4 to afford the corresponding highly functionalized, di- and trisubstituted homoallylic alcohols with high stereos

Full text of DOI:10.1016/S0040-4039(00)99420-6

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