✦ LIBER ✦

ChemInform Abstract: Reactivity of 3-Oxo-15-hexadecanolide.

✍ Scribed by A. SHARADENDU; L. WEILER

Publisher: John Wiley and Sons
Year: 2010
Weight: 31 KB
Volume: 29
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.199828197

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Diastereoselective

ChemInform Abstract: Diastereoselective Synthesis of 3-Oxo-14,15-dihydroandranginine.

✍ B. DANIELI; G. LESMA; M. MARTINELLI; D. PASSARELLA; A. SILVANI 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 35 KB

ChemInform Abstract: Studies with 3-Oxoa

ChemInform Abstract: Studies with 3-Oxoalkanonitriles: Synthesis and Reactivity of 3-Oxo-3-(1-methylindoloyl)propanenitrile.

✍ Haider Behbehani; Hamada Mohamed Ibrahim; Saad Makhseed 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 44 KB 👁 1 views

ChemInform Abstract: 3-Oxo-3-phosphapent

ChemInform Abstract: 3-Oxo-3-phosphapentopyranoses.

✍ C. J. R. FOOKES; M. J. GALLAGHER 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 28 KB

3-Oxo-3-phosphapentopyranoses. -Addition of methyl phosphinate (III) to dialdehyde (II), which is readily accessible by periodate cleavage of methyl β-D-arabinoside (I), affords 3-phosphapentopyranose (IV) as mixture of all eight possible diastereomers (no yield given). -(FOOKES, C.

ChemInform Abstract: Reactivity of 2-Sub

ChemInform Abstract: Reactivity of 2-Substituted 3-Ethylsulfonylpyridines.

✍ J. ROUCHAUD; O. NEUS; C. MOULARD 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 29 KB

Synthesis and Chemical Reactivity of 3-O

Synthesis and Chemical Reactivity of 3-Oxo-2-arylhydrazono-propanenitriles.

✍ Sanaa O. Abdallah; Nadia H. Metwally; Hany F. Anwar; Mohamed H. Elnagdi 📂 Article 📅 2005 🏛 John Wiley and Sons ⚖ 32 KB 👁 1 views

Synthesis and chemical reactivity of 3-o

Synthesis and chemical reactivity of 3-oxo-2-arylhydrazono-propanenitriles

✍ Sanaa O. Abdallah; Nadia H. Metwally; Hany F. Anwar; Mohamed H. Elnagdi 📂 Article 📅 2005 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 125 KB

## Abstract 2‐Formyl‐2‐arylhydrazonoethanenitriles **6b‐d** where prepared __via__ reacting enaminonitrile **2b,c** with aromatic diazonium salts. These reacted with phenylhydrazine to yield bis hydrazones that were converted to arylazopyr‐azoles via a novel Vilsmeier‐Haack reaction type. Reaction