𝔖 Bobbio Scriptorium
✦   LIBER   ✦

A simple method for the preparation of various 1-oxo-hydrindene-2-acetic and -propionic acids. Valuable precursors of strigol and its analogues

✍ Scribed by István Kádas; Géza Árvai; Lászlo Tőke; Gábor Tóth; Áron Szöllősy; Mária Bihari


Book ID
104204310
Publisher
Elsevier Science
Year
1994
Tongue
French
Weight
898 KB
Volume
50
Category
Article
ISSN
0040-4020

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✦ Synopsis


Abrtra~t: An improved annulaiion sequence is presented, making use of the one-pot cyclization of S-nitqentan-2one and cyclopeni-2-enone diesters to aflord 7-methyl-4-nitro-l-oxohydrindene derivatives. Functional group elaborations of these intermediates lead to a series of the title compounds, which could be readily converted to the tricyclic moieties of strigol and its analogaes of biological importance.


📜 SIMILAR VOLUMES


Chemistry of ketene acetals IV. A simple
✍ R. W. Aben; R. Hofstraat; J. W. Scheeren 📂 Article 📅 2010 🏛 Elsevier Science 🌐 English ⚖ 494 KB

## Abstract α‐Acyloxy aldehydes (**2a,b**) react with 1,1‐dimethoxypropene (**1**) in the presence of ZnCl~2~ to yield 2,2‐dimethoxy‐3‐methyloxetanes (**3a,b**). Stronger electron‐withdraxing acyl groups are necessary for the analogous conversion ofα‐acyloxy ketones (**2c,d,e**). Hydrolysis of the

Virtually Complete Control of Simple and