“…For example, pyrrole-3-carboxylic acid esters can be reduced to the corresponding 3-methylpyrroles by LiAlH 4 . 8,9 Besides that, we have found three examples [10][11][12] of one-pot synthesis of methyl derivatives from methyl carboxylates. The first example 10 concerned the reduction of methyl anthranilate by LiAlH 4 to methylaniline in 96 % yield, but the process takes 20 days at room temperature.…”
Section: Introductionmentioning
confidence: 95%
“…The first example 10 concerned the reduction of methyl anthranilate by LiAlH 4 to methylaniline in 96 % yield, but the process takes 20 days at room temperature. The second one 11 deals with the reduction of cinnamic acid esters by a mixture of LiAlH 4 and AlCl 3 . In this reaction, a mixture of the target compound and the product of allylic rearrangement was obtained in the ratio 2:1.…”
A method for the synthesis of methylthiophenes from various ketones has been elaborated. The target methylthiophenes were used for the synthesis of photochromic 1,2-dithienylethenes with heterocyclic bridges.
“…For example, pyrrole-3-carboxylic acid esters can be reduced to the corresponding 3-methylpyrroles by LiAlH 4 . 8,9 Besides that, we have found three examples [10][11][12] of one-pot synthesis of methyl derivatives from methyl carboxylates. The first example 10 concerned the reduction of methyl anthranilate by LiAlH 4 to methylaniline in 96 % yield, but the process takes 20 days at room temperature.…”
Section: Introductionmentioning
confidence: 95%
“…The first example 10 concerned the reduction of methyl anthranilate by LiAlH 4 to methylaniline in 96 % yield, but the process takes 20 days at room temperature. The second one 11 deals with the reduction of cinnamic acid esters by a mixture of LiAlH 4 and AlCl 3 . In this reaction, a mixture of the target compound and the product of allylic rearrangement was obtained in the ratio 2:1.…”
A method for the synthesis of methylthiophenes from various ketones has been elaborated. The target methylthiophenes were used for the synthesis of photochromic 1,2-dithienylethenes with heterocyclic bridges.
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