𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Studies on Thermal Reactivity of β-(1,2-Allenyl)butenolides and 2-Allyl-3-allenylcyclohex-2-enones

✍ Scribed by Zhenhua Gu; Shengming Ma

Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
484 KB
Volume
14
Category
Article
ISSN
0947-6539

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Thermal Reactivity
ChemInform Abstract: Thermal Reactivity of β-(1,2-Allenyl)butenolides and 2-Allyl-3-allenylcyclohex-2-enones.
✍ Zhenhua Gu; Shengming Ma 📂 Article 📅 2008 🏛 John Wiley and Sons ⚖ 62 KB

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v

Studies on Debenzylation and Photolysis
Studies on Debenzylation and Photolysis of 1-Benzyl- and 1-(β-Phenethyl)-1,2,3,4-tetrahydroisoquinolines
✍ T. R. Govindachari; K. Nagarajan; S. Rajeswari; H. Suguna; B. R. Pai 📂 Article 📅 1977 🏛 John Wiley and Sons 🌐 German ⚖ 793 KB

## Abstract Debenzylation of 1‐(3‐benzyloxybenzyl)‐1,2,3,4‐tetrahydroisoquinolines **1**, **6**, **7** with hydrochloric acid and ethanol gave the corresponding phenolic isoquinolines **2**, **8**, **9** and tetrahydroprotoberberines **4**, **12**, **13**. Compounds **2**, **8**, **9** on photolysi

Studies with enaminones: Synthesis and c
Studies with enaminones: Synthesis and chemical reactivity of 2-(4-dimethylamino-2-oxobut-3-enyl)-isoindole-1,3-dione and of 4-(4-dimethylamino-2-oxobut-3-enyloxy)-2H-phthalazin-1-one
✍ Saleh Al-Mousawi; Elizabeth John; Najat Al-Kandery 📂 Article 📅 2004 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 194 KB

## Abstract The title compounds were synthesized __via__ condensing acetonylphthalimide and 4‐acetonyloxyphthalazine‐1‐one with dimethylformamide dimethylacetal (DMFDMA). The reaction of these enaminones with electrophiles and nucleophiles is reported as a route to polyfunctional heteroaromatics.