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7-Thiatetracyclo[4.1.0.02,4.03,5]heptan (Benzvalensulfid) — Synthese und Reaktionen

✍ Scribed by Leininger, Hartmut ;Kemmer, Petra ;Beck, Karin ;Christl, Manfred

Publisher
Wiley (John Wiley & Sons)
Year
1982
Tongue
English
Weight
653 KB
Volume
115
Category
Article
ISSN
0009-2940

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📜 SIMILAR VOLUMES

Tetracyclo[4.1.0.02,4.03,5]heptanes from
Tetracyclo[4.1.0.02,4.03,5]heptanes from 7,8-Diazatetracyclo[4.3.0.02,4.03,5]non-7-enes
✍ Prof. Dr. Manfred Christl; Dipl.-Chem. Erich Brunn 📂 Article 📅 1981 🏛 John Wiley and Sons 🌐 English ⚖ 213 KB 👁 1 views

which is converted by cleavage of CO, into the products in a thermodynamic E/Z ratio (E/Z= 9/1). ## Tetracyclo [4.1.0.02~4.03~5)heptanes from 7,8-Diazatetracyclo14.3.0.0z~4.03~s~non-7-enes I\*\*]

X-Ray Structure Analysis of 6-Thiatetrac
X-Ray Structure Analysis of 6-Thiatetracyclo-[5.4.0.02.4.03.5]undeca-1(7),8,10-triene
✍ Dr. Chizuko Kabuto; Dipl.-Chem. Toshio Tatsuoka; Prof. Dr. Ichiro Murata; Prof. 📂 Article 📅 1974 🏛 John Wiley and Sons 🌐 English ⚖ 225 KB 👁 1 views

Arsabenzene-4-carbaldehyde ( 4 ) can be obtained pure as a pale yellow oil by bulb tube vacuum distillation (10-' torr). Surprisingly, the product, which is stable under nitrogen, smells strongly and unmistakably of benzaldehyde, thus providing further justification for the trivial name "arsabenzald