A Mild and Efficient Method for the Acetylation of Alcohols.
ChemInform Vol. 36, No. 19
Abstract For Abstract see ChemInform Abstract in Full Text.
DOI: 10.1002/chin.200519066کتابخانه علمی دکتر زلفی گل؛ دسترسی یکپارچه به مقالات، کتابها، DOI و اطلاعات استنادی گردآوریشده از منابع معتبر دانشگاهی
ChemInform Vol. 36, No. 19
Abstract For Abstract see ChemInform Abstract in Full Text.
DOI: 10.1002/chin.200519066ChemInform Vol. 36, No. 19
Abstract For Abstract see ChemInform Abstract in Full Text.
DOI: 10.1002/chin.200519096Journal of the Chinese Chemical Society Vol. 52, No. 2, 327–330
Aliphatic and aromatic 1,3-dithiane are oxidized to the corresponding carbonyl compounds in good yields under mild conditions by N,N′-diiodo-N,N′-1,2-ethanediyl-bis(p-toluenesulphonamide) [NIBTS] and silver nitrate.
DOI: 10.1002/jccs.200500049ChemInform Vol. 36, No. 16
Abstract For Abstract see ChemInform Abstract in Full Text.
DOI: 10.1002/chin.200516111ChemInform Vol. 36, No. 14
Abstract For Abstract see ChemInform Abstract in Full Text.
DOI: 10.1002/chin.200514062ChemInform Vol. 36, No. 13
DOI: 10.1002/chin.200513124ChemInform Vol. 36, No. 13
DOI: 10.1002/chin.200513057ChemInform Vol. 36, No. 13
Abstract For Abstract see ChemInform Abstract in Full Text.
DOI: 10.1002/chin.200513091ChemInform Vol. 36, No. 9
Abstract For Abstract see ChemInform Abstract in Full Text.
DOI: 10.1002/chin.200509060ChemInform Vol. 36, No. 8
Abstract For Abstract see ChemInform Abstract in Full Text.
DOI: 10.1002/chin.200508124ChemInform Vol. 36, No. 8
Abstract For Abstract see ChemInform Abstract in Full Text.
DOI: 10.1002/chin.200508134ChemInform Vol. 36, No. 7
DOI: 10.1002/chin.200507052ChemInform Vol. 36, No. 4
DOI: 10.1002/chin.200504096Synlett No. 7, 1155–1157
One-pot three-component condensation of isatoic anhydride with primary amines or ammonium carbonate and aromatic aldehydes in refluxing ethanol in the presence of catalytic amounts of silica sulfuric acid afforded the corresponding 2,3-dihy…
DOI: 10.1055/s-2005-865200Mendeleev Communications Vol. 15, No. 3, 113–116
Silica chromate easily converts primary and secondary alcohols to corresponding carbonyl compounds in the presence of wet SiO2 both in dichloromethane and under solvent-free conditions at room temperature with good to excellent yields. Prim…
DOI: 10.1070/mc2005v015n03abeh002005ChemInform Vol. 36, No. 3
DOI: 10.1002/chin.200503129ChemInform Vol. 36, No. 2
Abstract For Abstract see ChemInform Abstract in Full Text.
DOI: 10.1002/chin.200502054ChemInform Vol. 36, No. 1
Abstract For Abstract see ChemInform Abstract in Full Text.
DOI: 10.1002/chin.200501101ChemInform Vol. 35, No. 51
Abstract For Abstract see ChemInform Abstract in Full Text.
DOI: 10.1002/chin.200451056Bioorganic & Medicinal Chemistry Letters Vol. 14, No. 24, 6079–6082
DOI: 10.1016/j.bmcl.2004.09.070Synlett Vol. 2004, No. 15, 2803–2805
A rapid, mild and high-yielding method for dehydrogenation of a variety of structurally diverse 2-imidazolines to imidazoles using trichloroisocyanuric acid (TCCA) in the presence of DBU is reported. Chemoselective oxidation of 2-imidazolin…
DOI: 10.1055/s-2004-835635Phosphorus, sulfur, and silicon and the related elements Vol. 179, No. 11, 2273–2277
H 3 PMo 12 O 40 · xH 2 O was found to be an effective catalyst for the preparation of bis-indolyl derivatives from indole and aromatic, aliphatic, heterocyclic aldehydes or ketones in ethanol at room temperature.
DOI: 10.1080/10426500490484904Phosphorus, sulfur, and silicon and the related elements Vol. 179, No. 11, 2177–2182
Silica phosphoric acid was prepared via reaction of silica chloride (I) and phosphoric acid. Thiols can be readily converted to their corresponding thionitrites with a combination of silica phosphoric acid (II), wet SiO 2 , and sodium nitri…
DOI: 10.1080/10426500490474842Phosphorus, sulfur, and silicon and the related elements Vol. 179, No. 11, 2189–2193
Trimethylsilyl ethers were converted to their corresponding alcohols in the presence Nafion-H® and wet SiO 2 with good-to-excellent yields under mild and heterogeneous conditions.
DOI: 10.1080/10426500490474996