Efficient Synthesis of 6-Substitued-3-aminoestrogens
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چکیده
منابع مشابه
3-substitued indoles: one-pot synthesis and evaluation of anticancer and Src kinase inhibitory activities.
An efficient and economical method was developed for the synthesis of 3-substituted indoles by one-pot three-component coupling reaction of a substituted or unsubstituted benzaldehyde, N-methylaniline, and indole or N-methylindole using Yb(OTf)(3)-SiO(2) as a catalyst. All the synthesized compounds were evaluated for inhibition of cell proliferation of human colon carcinoma (HT-29), human ovari...
متن کاملSynthesis, Antitumor and Anti-inflammatory Activities of 2-thienyl-3-substitued Indole Derivatives
A series of 2-thienyl-3-substitued indole derivatives (1-11) were synthesized. Their structures were established on the basis of elemental and spectral (IR, HNMR and Mass spectral data) studies. All the 1 synthesized compounds have been tested for their antitumor activity against breast cancer cell line (MCF-7) using doxorubicin as a standard drug (IC =2.97 μg/ml). Most of the prepared compound...
متن کاملnano-rods zno as an efficient catalyst for the synthesis of chromene phosphonates, direct amidation and formylation of amines
چکیده ندارد.
Synthesis of 2-Substitued Benzimidazoles Using P2O5-SiO2
P2O5-SiO2 (30% w/w) was found to be a useful catalyst for the synthesis of various 2-substituted aryl benzimidazoles under solvent-less and in solvent conditions from o-phenylenediamine and aldehydes. The products were directly recrystallized from methanol.
متن کاملSynthesis of 2-Substitued Benzimidazoles Using P2O5-SiO2
P2O5-SiO2 (30% w/w) was found to be a useful catalyst for the synthesis of various 2-substituted aryl benzimidazoles under solvent-less and in solvent conditions from o-phenylenediamine and aldehydes. The products were directly recrystallized from methanol.
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ژورنال
عنوان ژورنال: Chinese Journal of Organic Chemistry
سال: 2017
ISSN: 0253-2786
DOI: 10.6023/cjoc201610005