𝔖 Bobbio Scriptorium
✦   LIBER   ✦

The conformation of cyclodeca-1,6-diene

✍ Scribed by David N.J. White; Moira J. Bovill

Publisher
Elsevier Science
Year
1975
Tongue
French
Weight
108 KB
Volume
16
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Irradiation of the cis,cis-cyclodeca-1,6
Irradiation of the cis,cis-cyclodeca-1,6-diene system
✍ Arnon Shani 📂 Article 📅 1968 🏛 Elsevier Science 🌐 French ⚖ 111 KB

The photoohemical reaction of g&,EQS";yoloocta-lr5-diene (I) yielded the cross-bonded tricycle [3.3.0.02'6] octane (II) (1) and that of the cyclohexa-1,4-diene III led to the rearranged bicyclic product IV (2). We wish to report the p$toohemical reaction of the &&&-cyclodeca-1,6-diene system (3), (

1,6-Dioxo-cyclodeca-3,8-dien und 1,6-Dia
1,6-Dioxo-cyclodeca-3,8-dien und 1,6-Diamino-cyclodeca-3,8-dien. Cyclodecapolyene, 1. Mitteilung
✍ C. A. Grob; P. W. Schiess 📂 Article 📅 1960 🏛 John Wiley and Sons 🌐 German ⚖ 712 KB

## 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).

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).

Crystal Structure Analysis of a trans, t
Crystal Structure Analysis of a trans, trans-Cyclodeca-1, 6-diene Derivative
✍ David N. J. White 📂 Article 📅 1973 🏛 John Wiley and Sons 🌐 German ⚖ 260 KB

## Abstract An X‐ray crystal structure analysis of the higher melting diastereoisomer of 2,7‐dibromo‐3,8‐dimethoxy‐__trans,trans__‐cyclodeca‐1,6‐diene (Monoclinic; __a__ = 5.76, __b__ = 10.43, __c__ = 11.32 Å, β = 94.04°; space group P2~1~/n; Z = 2) has confirmed the NMR. assignment of the molecula

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

Conformational study of the 4,9-dihetero
Conformational study of the 4,9-dihetero-(Z,Z)-cyclodeca-1,6-diene ring system; the mono- and di-benzo analogues
✍ E. Kleinpeter; J. Hartmann; W. Schroth 📂 Article 📅 1990 🏛 John Wiley and Sons 🌐 English ⚖ 563 KB

## Abstract The dynamic ^1^H and ^13^C NMR spectra of a series of mono‐ and bis‐annelated 4,9‐dihetero‐(__Z,Z__)‐cyclodeca‐1,6‐dienes were obtained and are discussed with respect to ground‐state conformers and the barriers to ring inversion, and to the restricted rotation about exocyclic partial C,