## Abstract magnified image 3,4‐Dihydro‐2‐H‐pyran and oxalyl chloride react, depending on the conditions, to keto esters, a pyran‐3‐carboxylic acid or derivatives thereof, or to an hitherto unknown bicyclic acetal containing a vinyl chloride moiety. The structure of the latter product has been una
Structure of an unexpected trimer from the reaction of ageratochromene II with aluminum chloride
✍ Scribed by Changhu Chu; Jiehan Hu; Tao XU; Hongbin Xiao; Xinmiao Liang
- Publisher
- John Wiley and Sons
- Year
- 2002
- Tongue
- English
- Weight
- 103 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0749-1581
- DOI
- 10.1002/mrc.1023
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
A new trimer from the reaction of ageratochromene [1] (6,7‐dimethoxy‐2,2‐dimethyl‐1‐benzopyran) with anhydrous aluminum chloride was shown to be 3,4‐dihydro‐6,7‐dimethoxy‐2,2‐dimethyl‐3‐(6′,7′‐dimethoxy‐2′,2′‐dimethyl‐2__H__‐1‐benzopyran‐4′‐yl)‐4‐(3′,4′‐dihydro‐6′, 7′‐dimethoxy‐2′,2′‐dimethyl‐2__H__‐1‐benzopyran‐3′‐yl)‐ 2__H__‐1‐benzopyran. Its structure was confirmed by NMR (^1^H, ^13^C, DEPT‐135. COSY, HMBC, HSQC, TOCSY and NOESY), IR, mass spectra and elemental analysis. Copyright © 2002 John Wiley & Sons, Ltd.
📜 SIMILAR VOLUMES
## Abstract The reaction of (I) with oxalyl chloride and selected nucleophilic reagents leads to the unexpected bicyclic product (IV) and/or dihydropyran carboxylic acid derivatives, e.g. (V) and (VIII).