نتایج جستجو برای: ester synthesis
تعداد نتایج: 440914 فیلتر نتایج به سال:
the synthesis of twenty five esters of testosterone (17β -hydroxyandrost- 4-en-3-one) is described. all esters are derivatives of cycloalkycarboxylic acids. some of the esters possess α- , β -and/or & - substitution in the ester side-chain. the work was undertaken in order to evaluate long-acting male antifertility effect of such esters. most of the compounds, especially compound no.1, were fou...
This study reports the synthesis and characterization of biobased CANs incorporating CF 3 -activated aza-Michael bonds ester groups showing remarkable reprocessing abilities high activation energy.
An improved, simple, and facile synthesis of 3,4-dihydropyrimidin-2(1H)-ones by employing three-component, one-pot condensation reaction of β-keto ester, aromatic aldehydes, and urea or N-methylurea using LaCl3/ClCH2COOH as an inexpensive and green chemistry catalyst system under solvent-free conditions described. Compared with the classicalBiginelli reaction conditions, this method has the adv...
The synthesis of twenty five esters of testosterone (17β -hydroxyandrost- 4-en-3-one) is described. All esters are derivatives of cycloalkycarboxylic acids. Some of the esters possess α- , β -and/or & - substitution in the ester side-chain. The work was undertaken in order to evaluate long-acting male antifertility effect of such esters. Most of the compounds, especially compound No.1, wer...
The yield and purity of synthetic peptides were greatly related to the amino acid protection and activation during the synthesis process. Therefore, the amino acid protection and activation are the most important steps in peptide synthesis. By using tetrahydrofuran as the solvent, 9-fluorenylmethoxycarbonyl as protection group, 2-(7-azobenzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorop...
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