## Abstract A simple, highly selective transformation of 5,6,7,8‐tetrahydro‐2__H__‐1‐benzopyran‐2,5‐diones 1–3 and 14 with some phenylhydrazines and heterocyclic hydrazines to 5‐hydrazono‐2__H__‐1‐benzopyran‐2‐ones 4–12 and 15–16 is described. Under more severe conditions the hydrazonoquinoline der
Investigation of the one-pot synthesis ofN-(5,6,7,8-tetrahydro-7,7-dimethyl-2,5-dioxo-2H-1-benzopyran-3-yl-2,5-dioxo-2H-1-benzopyran-3-yl)benzamide
✍ Scribed by Kočevar, Marijan ;Polanc, Slovenko ;Verček, Bojan ;Tišler, Miha
- Publisher
- John Wiley and Sons
- Year
- 1990
- Tongue
- English
- Weight
- 294 KB
- Volume
- 1990
- Category
- Article
- ISSN
- 0947-3440
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✦ Synopsis
Abstract
A detailed investigation of the reaction of hippuric acid (2) with dimedone (1) and triethyl orthoformate or other one‐carbon sources in acetic anhydride yielding the benzopyran derivative 3 and many byproducts is described. An explanation of this complex process, several attempts to optimize it, and some new approaches to 3 are given.
📜 SIMILAR VOLUMES
I211 Genbve 4 (5. V .86) ~ Comparative results on the reduction of 4,6,7,8-tetrahydro-7,7-dimethyl-2H-1 -benzopyran-2,5(3H)-diones 1 are reported. Hydride reduction (LiAIH, in EtzO or NaBH, in i-PrOH) affords 2,3,4,6,7,8-hexahydro-5H-l-benzopyran-5-ones 5 in 30-60 % isolated yield. Photochemical red
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