✦ LIBER ✦

4,6,7-Trimethoxyfuro[2,3-b]quinoline–water (2/3)

✍ Scribed by Latip, Jalifah ;Ali, Noor Hapeedah M. ;Yamin, Bohari M.

Publisher: International Union of Crystallography
Year: 2005
Tongue: English
Weight: 276 KB
Volume: 61
Category: Article
ISSN: 1600-5368
DOI: 10.1107/s1600536805019082

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Synthesis of 4-methyl furo(2,3-b)quinoli

Synthesis of 4-methyl furo(2,3-b)quinoline

✍ P. Shanmugam; P. Lakshminarayana 📂 Article 📅 1971 🏛 Elsevier Science 🌐 French ⚖ 114 KB

The previous paper0 l-3 from thio laboratory describe the synthesis of 213 dihydrofuro(2,3-b)quinolines , and in no cane oould the dihydro compound be dehydrogeaated to the furoquinoline. The poaeibility that 3-vinyl-2-quinolones might oerve aa nece#aary precursor6 for the syntheaie of furo(2,3-b)qu

2,3,3a,4,5,9b-Hexahydro-4-phenylfuro[3,

2,3,3a,4,5,9b-Hexahydro-4-phenylfuro[3,2-c]quinoline

✍ Ravikumar, K. ;Sridhar, B. ;Mahesh, M. ;Narayana Reddy, V. V. 📂 Article 📅 2006 🏛 International Union of Crystallography 🌐 English ⚖ 141 KB

Benzo[f]furo[3,4-c][2,7]naphthyridines f

Benzo[f]furo[3,4-c][2,7]naphthyridines from Furo[3,4-b]-pyridines.

✍ K. Goerlitzer; U. Bartke 📂 Article 📅 2003 🏛 John Wiley and Sons ⚖ 194 KB 👁 1 views

New Pathway to Furo[2,3-b]quinoline Deri

New Pathway to Furo[2,3-b]quinoline Derivatives.

✍ V. F. Traven; N. Ya. Podkhalyuzina; D. S. Kanevskii 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 28 KB

4-(4-Nitrophenyl)-2,3,3a,4,5,9b-hexah

4-(4-Nitrophenyl)-2,3,3a,4,5,9b-hexahydrofuro[3,2-c]quinoline

✍ Ravikumar, K. ;Sridhar, B. ;Mahesh, M. ;Reddy, V. V. Narayana 📂 Article 📅 2005 🏛 International Union of Crystallography 🌐 English ⚖ 275 KB

Untersuchungen an Siebenring-Systemen, X

Untersuchungen an Siebenring-Systemen, XII Versuche in der 2.3.4-Trimethoxy-7H-benzocyclohepten-Reihe: 2.3.4-Trimethoxy-6.7-dehydro-8.9-dihydro-7H-benzocyclohepten und 6-Brom-2.3.4-trimethoxy-8.9-dihydro-7H-benzocyclohepten-7-on2)

✍ Tochtermann, Werner ;Schäfer, Dieter ;Pfaff, Diethelm 📂 Article 📅 1973 🏛 Wiley (John Wiley & Sons) ⚖ 570 KB

## Abstract Die Bromwasserstoff‐Eliminierung mit Kalium‐tert.‐butanolat aus 6‐Brom‐2.3.4‐trimethoxy‐8.9‐dihydro‐7__H__‐benzocyclohepten (**3b**) führt zum Cycloallen **5**, das mit 1.3‐Diphenyl‐benzo‐[__c__]furan (**6**) das Addukt **8** ergibt. In Abwesenheit von Abfängern dimerisiert **5**; die K

4,6,7-Trimethoxy­furo[2,3-b]quinoline–water (2/3)

4,6,7-Trimethoxyfuro[2,3-b]quinoline–water (2/3)