benzofurans and methyl-iodide

benzofurans has been researched along with methyl-iodide* in 1 studies

Other Studies

1 other study(ies) available for benzofurans and methyl-iodide

Article	Year
Formal synthesis of (+)-3-epi-eupomatilone-6 and the 3,5-bis-epimer. Organic & biomolecular chemistry, 2014, Sep-21, Volume: 12, Issue:35 The formal synthesis of (+)-3-epi-eupomatilone-6 () and the 3,5-bis-epimer () has been accomplished. The key synthetic strategy involved the stereoselective construction of (3R,4S,5R)- and (3R,4S,5S)-trisubstituted γ-butyrolactones and from (2R,3R)-2,3-dimethyl-4-pentenoic acid derivative , which was readily obtained via stereoselective conjugate addition of vinylmagnesium chloride to a chiral α,β-unsaturated N-acyl oxazolidinone (Evans' auxiliary) followed by α-methylation. Topics: Benzofurans; Chemistry, Pharmaceutical; Chlorides; Drug Design; Hydrocarbons, Iodinated; Lactones; Magnesium Chloride; Magnetic Resonance Spectroscopy; Methylation; Molecular Structure; Plant Extracts; Stereoisomerism	2014

Article

Year

Formal synthesis of (+)-3-epi-eupomatilone-6 and the 3,5-bis-epimer.

Organic & biomolecular chemistry, 2014, Sep-21, Volume: 12, Issue:35

The formal synthesis of (+)-3-epi-eupomatilone-6 () and the 3,5-bis-epimer () has been accomplished. The key synthetic strategy involved the stereoselective construction of (3R,4S,5R)- and (3R,4S,5S)-trisubstituted γ-butyrolactones and from (2R,3R)-2,3-dimethyl-4-pentenoic acid derivative , which was readily obtained via stereoselective conjugate addition of vinylmagnesium chloride to a chiral α,β-unsaturated N-acyl oxazolidinone (Evans' auxiliary) followed by α-methylation.

Topics: Benzofurans; Chemistry, Pharmaceutical; Chlorides; Drug Design; Hydrocarbons, Iodinated; Lactones; Magnesium Chloride; Magnetic Resonance Spectroscopy; Methylation; Molecular Structure; Plant Extracts; Stereoisomerism

2014