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[3+2]-Cycloaddition of Nitrile Imines to Parabanic Acid Derivatives—An Approach to Novel Spiroimidazolidinediones bonds is a convenient method of creating spiro-conjugated molecules with promising anticancer activity

Chemical and Biological Evaluation of Novel 1H-Chromeno[3,2-c]pyridine Derivatives as MAO Inhibitors Endowed with Potential Anticancer Activity fragments at C10, as well as a few small substituents at C6 and C8, were synthesized starting from 1

Selective cross-dehydrogenative C-O coupling of: N -hydroxy compounds with pyrazolones. Introduction of the diacetyliminoxyl radical into the practice of organic synthesis sterically unhindered; it was isolated from an oxidant and used as a new reagent for the synthesis

Hydrogen bonding in hydroxypyridium salts

Some reactions of 8,11,11-trimethyl-11-silabenzo[b]naphtho[2,3-d]thiophen-6-one involving the carbonyl group

Pseudo Four-Component Synthesis of 5,6-Dihydroindolo[2,1-a]isoquinolinesAn easy synthesis of novel highly functionalized 5,6-dihydroindolo[2,1-a

Synthesis and crystal structure of 7,7,10-trimethyl-7-silabenzo[a]anthroneSynthesis and crystal structure of 7,7,10-trimethyl-7-silabenzo[a]anthrone

Hydrogen bonding in hydroxypyridium salts) a=4.6477(2), b=14.5906(9), c=14.5551(8) Å, β=99.100(4)°, space group P21/c, Z=4, Rp/Rwp=0

Molecular recognition of organic vapors by adamantylcalix[4]arene in QCM sensor using partial binding reversibility determined for clathrates of adamantylcalix[4]arene (1), These data provide a new insight into the structure

Molecular recognition of organic vapors by adamantylcalix[4]arene in QCM sensor using partial binding reversibility determined for clathrates of adamantylcalix[4]arene (1), These data provide a new insight into the structure

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