✦ LIBER ✦

A new use of the birch reduction. Synthesis of 2,3-disubstituted cyclopent-2-en-1-ones from 6-methoxyindanone

✍ Scribed by Christopher J. Moody; Judy Toczek

Publisher: Elsevier Science
Year: 1986
Tongue: French
Weight: 112 KB
Volume: 27
Category: Article
ISSN: 0040-4039
DOI: 10.1016/s0040-4039(00)85182-5

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

The Vilsmeier-Haack reaction with 3,4-di

The Vilsmeier-Haack reaction with 3,4-disubstituted isoxazolin-5-ones. A new synthesis of 1,3-oxazin-6-ones and 1,3-oxazine-2,6-diones.

✍ Egle M. Beccalli; Alessandro Marchesini; Henriette Molinari 📂 Article 📅 1986 🏛 Elsevier Science 🌐 French ⚖ 182 KB

Vilsmeier-Haack type reaction on isoxazolin-5-ones is presented. Recently described is zin-6-ones. 2 The synthetic We report here on the the preparation of a number of E-amino-' and 2-phenyl-6H-1,3-oxapotential of such a class of compounds is well documented.3 syntheses by a Vilsmeier-Haack type rea

A new highly diastereoselective synthesi

A new highly diastereoselective synthesis of 2,5-disubstituted-1,3-dioxolan-4-ones from α-hydroxyacids

✍ N. Chapel; A. Greiner; J-Y. Ortholand 📂 Article 📅 1991 🏛 Elsevier Science 🌐 French ⚖ 114 KB

One-Pot Synthesis of a New Series of 3-A

One-Pot Synthesis of a New Series of 3-Alkoxy-5-hydroxy-5-trifluoromethylpyrrolidin-2-ones from 1,1,1-Trifluoro-4-alkoxyalk-3-en-2-ones.

✍ Nilo Zanatta; Luciana S. Rosa; Maria F. M. Cortelini; Simone Beux; Ana P. D. San 📂 Article 📅 2003 🏛 John Wiley and Sons ⚖ 136 KB 👁 2 views

A Novel Synthesis of 2-Alkoxy-3-hydroxyt

A Novel Synthesis of 2-Alkoxy-3-hydroxytropones and 2,7-Dihydroxytropones from Dialkoxy-8-oxabicyclo[3.2.1]oct-6-en-3-ones.

✍ Hartmut Zinser; Sonja Henkel; Baldur Foehlisch 📂 Article 📅 2004 🏛 John Wiley and Sons ⚖ 312 KB 👁 1 views

A Novel Synthesis of 2-Alkoxy-3-hydroxyt

A Novel Synthesis of 2-Alkoxy-3-hydroxytropones and 2,7-Dihydroxytropones from Dialkoxy-8-oxabicyclo[3.2.1]oct-6-en-3-ones

✍ Hartmut Zinser; Sonja Henkel; Baldur Föhlisch 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 286 KB 👁 1 views

## Abstract Trichloro‐substituted 8‐oxabicyclo[3.2.1]oct‐6‐en‐3‐ones **6** and **7** are solvolysed by methanolic sodium methoxide to form the bicyclo[3.2.1] α,α‐dimethoxy ketones **13** and **14**, with preservation of one chloro substituent. In the case of **6a**, prolonged reaction time with an

The synthesis of 1,2,3-trichloro- and 2,

The synthesis of 1,2,3-trichloro- and 2,3-dichlorobicyclo[2.2.1]hept-2-en-7-one. A selective reduction of bridgehead chlorine.

✍ William H. Okamura; James F. Monthony; Curtis M. Beechan 📂 Article 📅 1969 🏛 Elsevier Science 🌐 French ⚖ 209 KB