✦ LIBER ✦

A novel reaction of 2,4,6-triphenyl(thio)selenopyrylium salts leading to benzoyl(thio)selenophenes and 2,4,6-triphenyl(thio)selenopyrans

✍ Scribed by B. I. Drevko; E. G. Bol’shakova; A. F. Almaeva; M. A. Suchkov; V. G. Mandych; G. A. Shekhter

Publisher: Springer
Year: 2009
Tongue: English
Weight: 211 KB
Volume: 58
Category: Article
ISSN: 1573-9171
DOI: 10.1007/s11172-009-0207-z

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: A Novel Reaction of

ChemInform Abstract: A Novel Reaction of 2,4,6-Triphenyl(thio)selenopyrylium Salts Leading to Benzoyl(thio)selenophenes and 2,4,6-Triphenyl(thio)selenopyrans.

✍ B. I. Drevko; E. G. Bol'shakova; A. F. Almaeva; M. A. Suchkov; V. G. Mandych; G. 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 18 KB

ChemInform Abstract: 2-Substituted Thio-

ChemInform Abstract: 2-Substituted Thio- and Amino-5,6-dimethoxy-1,4-naphthoquinones as a Novel Class of Acyl-CoA: Cholestrol Acyltransferase Inhibitors.

✍ Yongseok Choi; et al. et al. 📂 Article 📅 2009 🏛 John Wiley and Sons ⚖ 28 KB 👁 1 views

Synthesis of chloro (diethylalkoxyphosph

Synthesis of chloro (diethylalkoxyphosphine) gold (I) salts and their subsequent conversion to s-diethylalkoxyphosphine gold 2,3,4,6-tetra-o-acetyl-thio-β-D-glucopyranosides

✍ F. Owings; E.L. Anderson; W.W. Holl; L.B. Killmer Jr. 📂 Article 📅 1982 🏛 Elsevier Science 🌐 French ⚖ 171 KB

A novel alkoxy-interchange leading to a variety of alkoxy phosphine-gold-chlorides from one common starting material is reported. In continuation of our studies of general methods for synthesizing phosphine-gold complexes as possible anti-arthritic agents', a homologous series of diethylalkoxyphosph

Mechanism of the Thermal 1,3-Cyclohexadi

Mechanism of the Thermal 1,3-Cyclohexadiene Dimerization: A Non-Concerted Diels-Alder Reaction Leading to the exo-[4+2] Adduct and a Novel [6+4]-Ene Reaction

✍ Prof. Dr. Frank-Gerrit Klärner; Dr. Barbara M. J. Dogan; Priv.-Doz. Dr. Otto Erm 📂 Article 📅 1986 🏛 John Wiley and Sons 🌐 English ⚖ 379 KB 👁 2 views

A novel aldol-type C-glycosidation react

A novel aldol-type C-glycosidation reaction promoted by samarium diiodide. Regioselective generation of a ulose-1-enolate from phenyl 3,4,6-tri-O-benzyl-1-thio-β-d-arabino-hexopyranosid-2-ulose

✍ Satoshi Ichikawa; Satoshi Shuto; Akira Matsuda 📂 Article 📅 1998 🏛 Elsevier Science 🌐 French ⚖ 231 KB

ChemInform Abstract: A Novel Aldol-Type

ChemInform Abstract: A Novel Aldol-Type C-Glycosidation Reaction Promoted by Samarium Diiodide. Regioselective Generation of a Ulose-1-enolate from Phenyl 3,4,6-Tri-O-benzyl-1-thio-β-D-arabino-hexopyranosid-2-ulose.

✍ S. ICHIKAWA; S. SHUTO; A. MATSUDA 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 37 KB 👁 1 views