2008
DOI: 10.1016/j.tetlet.2008.08.072
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Ionic liquid-promoted one-pot oxidative Michael addition of TMSCN to Baylis–Hillman adducts

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Cited by 45 publications
(28 citation statements)
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“…The chemical shifts for the 1 H in the benzoate group are also clearly evident. 13 Table 2 also confirm the characterization of this ionic liquid.…”
Section: H and 13 C Nmr Spectrasupporting
confidence: 68%
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“…The chemical shifts for the 1 H in the benzoate group are also clearly evident. 13 Table 2 also confirm the characterization of this ionic liquid.…”
Section: H and 13 C Nmr Spectrasupporting
confidence: 68%
“…The 1 H and 13 Tables 2 and 3, respectively, together with their assignments. The chemical shifts of the protons assigned to the [bmim] group agree well with that reported in the literature by Bonhote et al [28] (except that for C8) and clearly confirms the presence of this cation group.…”
Section: H and 13 C Nmr Spectramentioning
confidence: 99%
See 1 more Smart Citation
“…9 Ionic liquid and microwave have also been applied to this reaction in line of the concept of green chemistry. 10,11 Recently, Shibasaki and co-workers developed an entirely distinct Ni(0)-cyclooctdiene (COD) complex in the elegant synthesis of Tamiflu, 12 an anti-influenza drug, and subsequent Ni(0) and Gd(OTf) 3 as the cooperative catalyst in the 1,4-addition of Me 3 SiCN to aliphatic enones with good substrate generality. 13 The first catalytic enantioselective version of conjugate addition of cyanide to enones is also described by Shibasaki.…”
Section: Methodsmentioning
confidence: 99%
“…9 Ionic liquid and microwave have been utilized in this reaction in line of the concept of green chemistry. 10,11 Recently, Shibasaki and co-workers applied an entirely distinct Ni(0)-cyclooctadiene (COD) complex to the elegant synthesis of Tamiflu, 12 an important anti-influenza drug, and subsequent Ni(0) and Gd(OTf) 3 as the cooperative catalyst to the 1,4-addition of TMSCN to a wide variety of aliphatic enones. 13 The first synthetically useful catalytic enantioselective conjugate addition of cyanide to enones is also documented by Shibasaki.…”
Section: Equationmentioning
confidence: 99%