The 1,3 O→C silyl rearrangement of silyl enol ether anions - synthesis of α-silyl ketones.
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The 1,3 O→C silyl rearrangement of silyl enol ether anions - synthesis of α-silyl ketones. / Corey, E.J.; Rücker, Christoph.
In: Tetrahedron Letters, Vol. 25, No. 39, 1984, p. 4345-4348.Research output: Journal contributions › Journal articles › Research › peer-review
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TY - JOUR
T1 - The 1,3 O→C silyl rearrangement of silyl enol ether anions - synthesis of α-silyl ketones.
AU - Corey, E.J.
AU - Rücker, Christoph
PY - 1984
Y1 - 1984
N2 - Silyl enol ethers with sterically hindered silyl groups are transformed into the corresponding α-silyl ketones by treatment with n-butyllithium/potassium tert-butylate.
AB - Silyl enol ethers with sterically hindered silyl groups are transformed into the corresponding α-silyl ketones by treatment with n-butyllithium/potassium tert-butylate.
KW - Chemistry
U2 - 10.1016/S0040-4039(01)81434-9
DO - 10.1016/S0040-4039(01)81434-9
M3 - Journal articles
VL - 25
SP - 4345
EP - 4348
JO - Tetrahedron Letters
JF - Tetrahedron Letters
SN - 0040-4039
IS - 39
ER -