
Chemistry Letters p. 447 - 450 (1985)
Update date:2022-08-04
Topics:
Mukaiyama, Teruaki
Kobayashi, Shu
Murakami, Masahiro
Threo cross-aldol products are predominantly formed in good yields by treating tert-butyldimethylsilyl enol ethers with aldehydes in the presence of a catalytic amount of trityl perchlorate.
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Doi:10.1021/jo00350a084
(1985)Doi:10.1016/S0040-4039(00)89274-6
(1985)Doi:10.1590/S0103-50532010000900003
(2010)Doi:10.1039/PS9590000109
(1959)Doi:10.1021/acs.jmedchem.1c00491
(2021)Doi:10.1248/cpb.43.1391
(1995)