✦ LIBER ✦

Microwave-Assisted Synthesis of Substituted Naphtho[2,3-c]furan-1,3-dione Derivatives

✍ Scribed by Kawano, Tomikazu; Ishikawa, Yu; Hatanaka, Minoru

Book ID: 118247496
Publisher: Japan Institute of Heterocyclic Chemistry
Year: 2012
Tongue: English
Weight: 731 KB
Volume: 85
Category: Article
ISSN: 0385-5414
DOI: 10.3987/com-12-12429

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Microwave-Assisted

ChemInform Abstract: Microwave-Assisted Synthesis of Substituted Naphtho[2,3-c]furan-1,3-dione Derivatives.

✍ Tomikazu Kawano; Yu Ishikawa; Minoru Hatanaka 📂 Article 📅 2012 🏛 John Wiley and Sons ⚖ 34 KB

Synthesis of derivatives of naphtho[2,3-

Synthesis of derivatives of naphtho[2,3-b]furan-4,9-dione

✍ A. N. Grinev; S. A. Zotova 📂 Article 📅 1970 🏛 Springer US 🌐 English ⚖ 307 KB

Synthesis of tetra-substituted furan der

Synthesis of tetra-substituted furan derivatives from 1-arylpropane-2,3-diones

✍ A. M. Jones; A. J. Simpson; S. P. Stanforth 📂 Article 📅 1990 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 93 KB

ChemInform Abstract: Short-Step Synthesi

ChemInform Abstract: Short-Step Synthesis of 1,3-Disubstituted Naphtho[2,3-c]furan-4,9-dione and Naphtho[2,3-b]furan-4,9-dione by the Friedel—Crafts Reaction.

✍ J. KOYAMA; I. TOYOKUNI; A. KINO; K. TAGAHARA 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 31 KB 👁 1 views

Novel Methods of Synthesizing Naphtho[1,

Novel Methods of Synthesizing Naphtho[1,2-c]furan-1,3-dione and Benzo[e]isoindole-1,3-dione.

✍ Masahiro Mizuno; Mitsuhisa Yamano 📂 Article 📅 2006 🏛 John Wiley and Sons ⚖ 17 KB 👁 1 views

Solvent-free microwave-assisted synthesi

Solvent-free microwave-assisted synthesis of 1H-indole-2, 3-dione derivatives

✍ Ashish Kumar Singh; Sudhish Kumar Shukla; Ishtiaque Ahamad; M. A. Quraishi 📂 Article 📅 2009 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 66 KB 👁 1 views

## Abstract magnified image Microwave‐assisted synthesis has been found to increase both reaction rates and yields __via__ more efficient heating compared with standard thermal conduction. Dry reaction of isatins with thiosemicarbazide and their thiosemicarbazone with secondary amine on acid—washe