Retro-Ene Reaction. Part 5. Functionalization of 4,5-Dihalopyridazin-6-ones Using 1-Hydroxymethyl-4,5-dihalopyridazin-6-ones as 1-O, 3-N, 5-O Ene Adducts. -Functionalization of title compounds (I) via a retro-ene reaction with some nucleophiles affords exclusively 4-halo substituted products such
Retro-ene reaction. V. Functionalization of 4,5-dihalopyridazin-6-ones using 1-hydroxymethyl-4,5-dihalopyridazin-6-ones as 1–0, 3-n, 5–0 ene-adducts
✍ Scribed by Hyun-A Chung; Young-Jin Kang; Joo-Wha Chung; Su-Dong Cho; Yong-Jin Yoon
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 1999
- Tongue
- English
- Weight
- 315 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0022-152X
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Functionalization of 1‐hydroxymethyl‐4,5‐dihalopyridazin‐6‐ones via a retro‐ene reaction with some nucleophiles gave regioselectively only 5‐halo‐4‐substitutedpyridazin‐6‐ones.
📜 SIMILAR VOLUMES
## Abstract Functionalization of 1‐acetyloxymethyl‐4,5‐dihalopyridazin‐6‐ones __via__ retro‐ene reaction with some nucleophiles gave regioselectively only 5‐halo‐4‐substitutedpyridazin‐6‐ones.
Retro-Ene Reaction. Part 6. Functionalization of 4,5-Dihalopyridazin-6-ones Using 1-Acetyloxymethyl-4,5-dihalopyridazin-6-ones as the 1-O, 3-N, 5-O Ene-Adduct. -The synthesis and storage of the known 1-hydroxymethyl derivative of (I) is difficult. Thus, the functionalization of 4,5-dihalopyridazin-
## Abstract Functionalization of 4,5‐dihalopyridazin‐6‐ones using 1‐(1,1‐dibromo‐2‐oxopropyl)‐4,5‐dihalopyridazin‐6‐ones with some nucleophiles gave regioselectively only 5‐halo‐4‐substituted‐pyridazin‐6‐ones.