✦ LIBER ✦

1,6-Dioxo-cyclodeca-3,8-dien und 1,6-Diamino-cyclodeca-3,8-dien. Cyclodecapolyene, 1. Mitteilung

✍ Scribed by C. A. Grob; P. W. Schiess

Publisher: John Wiley and Sons
Year: 1960
Tongue: German
Weight: 712 KB
Volume: 43
Category: Article
ISSN: 0018-019X
DOI: 10.1002/hlca.19600430612

No coin nor oath required. For personal study only.

✦ Synopsis

Abstract

1,6‐Dioxo‐cyclodeca‐3,8‐diene (4) and the cis and trans forms of 1,6‐diamino‐cyclodeca‐3,8‐diene (7) have been synthesized from naphthalene via isotetralin (1). No transannular reaction was observed during the reduction of the dioxime of (4) to the diamine (7).

📜 SIMILAR VOLUMES

Photolytic transformations of cis, cis-c

Photolytic transformations of cis, cis-cyclodeca-3, 8-diene-1, 6-dione

✍ Jerry W. Stankorb; Kenneth Conrow 📂 Article 📅 1969 🏛 Elsevier Science 🌐 French ⚖ 186 KB

The recent communication by Shani (1) in which the photolysis of cis, cis-cyclodeca---3,8-diene-1, 6-dione (I) is reported to give cis,\*, cis-tricyclo[5. 3. 0. 0 2, (+d ecane-4,9--dione prompts us to report results we had obtained independently which lead to the cis, -anti, cis (IIa) stereochemical

Solution photochemistry. I. The photolys

Solution photochemistry. I. The photolysis of cis,cis-cyclodeca-3,8-diene-1,6-dione.

✍ John R. Scheffer; Mel L. Lungle 📂 Article 📅 1969 🏛 Elsevier Science 🌐 French ⚖ 195 KB

A study of the photochemistry of cis cis-cyclodeca-3,8-diem-1,6-dione (I) has recently -Ireported (1). We have been independently engaged in studying the photochemistry of I and present our results which differ significantly from those previously reported (1).

Synthesis and Properties of 1,6-Difuncti

Synthesis and Properties of 1,6-Difunctionalized Cyclodeca-3,8-diynes.

✍ Sheela Kochuparambil Chellappan; Gebhard Haberhauer; Sven Feuerbacher; Frank Rom 📂 Article 📅 2003 🏛 John Wiley and Sons ⚖ 94 KB 👁 1 views

On the Purported Structure of Cyclodeca[

On the Purported Structure of Cyclodeca[1,2,3-de: 6,7,8-d′e′]dinaphthalene

✍ Rolf Gleiter; Hans Peter Schaaff; Hans Rodewald; Reiner Jahn; Hermann Irngarting 📂 Article 📅 1987 🏛 John Wiley and Sons 🌐 German ⚖ 414 KB

Intramolecular photocyclization of cis,

Intramolecular photocyclization of cis, cis- and trans, trans-cyclodeca-1,6-diene to anti tricyclo[5.3.0.02,6]decane.

✍ Arnon Shani 📂 Article 📅 1972 🏛 Elsevier Science 🌐 French ⚖ 131 KB

The transannular photocyclization of the cis,cis-cyclodecs-1,6+lienes to the tricyolo 5.3.0.02p6 --C 3 decane (1) may be explained due to the proximity in space of the two double bonds in the ~~hamnocks conformation I (2). Hence, in an intramolecular photocyclization of the isomeric trans,trans,cycl

Inhaltsstoffe des Osmanthus-Absolues. 1.

Inhaltsstoffe des Osmanthus-Absolues. 1. Mitteilung: 2,5-Epoxy-megastigma-6,8-dien

✍ Roman Kaiser; Dietmar Lamparsky 📂 Article 📅 1978 🏛 John Wiley and Sons 🌐 German ⚖ 611 KB

**Constituents of __Osmanthus__ Absolute, Ist communication:2,5‐Epoxy‐megastigma‐6,8‐dienes** Besides some further ionone derivatives we identified two new bicyclic oxacompounds (**1a**/**1b**) of the megastigmane type in the Osmanthus absolute. Isolation, special features of their spectral datas a