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Regioselective ring opening by propanethiolate of (methylenedioxy)benzenes with electron-withdrawing substituents

✍ Scribed by Bruce K. Cassels; Claudemir Radetski; Marcos Caroli Rezende


Book ID
104589457
Publisher
Elsevier Science
Year
2010
Tongue
English
Weight
321 KB
Volume
111
Category
Article
ISSN
0165-0513

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✦ Synopsis


Abstract

The ring opening reaction of (methylenedioxy)benzenes 1 with propanethiolate in DMF leads to products 2 and/or 3, depending on the nature of the electron‐withdrawing substituent Z.


πŸ“œ SIMILAR VOLUMES


Organic Reactions Using Sodium Hydrogent
✍ Masakazu Yamashita; Yoshifumi Tanaka πŸ“‚ Article πŸ“… 1996 πŸ› John Wiley and Sons 🌐 English βš– 194 KB πŸ‘ 2 views

Aromatic aldehydes or ketones which have electron-withdrawing groups on the benzene ring were selectively reduced to the corresponding alcohols in good yields by sodium hydrogentelluride; common aldehydes such as benzaldehyde and tolualdehyde were inert.