Lanthanoid triflate-promoted indium- or zinc-mediated allylation of aminoaldehyde in aqueous media: Stereoselective route to β-aminoalcohols

Teck Peng Loh; Rui Bin Wang; Kee Leng Tan; Keng Yeow Sim

Lanthanoid triflate-promoted indium- or zinc-mediated allylation of aminoaldehyde in aqueous media: Stereoselective route to β-aminoalcohols

Teck Peng Loh, Rui Bin Wang, Kee Leng Tan, Keng Yeow Sim

National University of Singapore

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19 引用（Scopus）

摘要

Lanthanide triflate-promoted indium- or zinc- mediated allylations of α-aminoaldehyde in aqueous media have been developed and shown to obtain high level of anti-diastereofacial selectivity by the judicious choice of the amino-protecting group, Lewis acid and solvent employed.

源语言	英语
页（从-至）	237-240
页数	4
期刊	Main Group Metal Chemistry
卷	20
期	4
出版状态	已出版 - 1997
已对外发布	是

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abstract = "Lanthanide triflate-promoted indium- or zinc- mediated allylations of α-aminoaldehyde in aqueous media have been developed and shown to obtain high level of anti-diastereofacial selectivity by the judicious choice of the amino-protecting group, Lewis acid and solvent employed.",

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T2 - Stereoselective route to β-aminoalcohols

AU - Loh, Teck Peng

AU - Wang, Rui Bin

AU - Tan, Kee Leng

AU - Sim, Keng Yeow

PY - 1997

Y1 - 1997

N2 - Lanthanide triflate-promoted indium- or zinc- mediated allylations of α-aminoaldehyde in aqueous media have been developed and shown to obtain high level of anti-diastereofacial selectivity by the judicious choice of the amino-protecting group, Lewis acid and solvent employed.

AB - Lanthanide triflate-promoted indium- or zinc- mediated allylations of α-aminoaldehyde in aqueous media have been developed and shown to obtain high level of anti-diastereofacial selectivity by the judicious choice of the amino-protecting group, Lewis acid and solvent employed.

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M3 - 文章

AN - SCOPUS:0000343666

SN - 0792-1241

VL - 20

SP - 237

EP - 240

JO - Main Group Metal Chemistry

JF - Main Group Metal Chemistry

IS - 4

ER -

Lanthanoid triflate-promoted indium- or zinc-mediated allylation of aminoaldehyde in aqueous media: Stereoselective route to β-aminoalcohols

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