✦ LIBER ✦

Sulphur participation in elimination reactions of 9-thiabicyclo[3.3.1]Nonanes

✍ Scribed by Peter H. McCabe; C. Mary Livingston

Publisher: Elsevier Science
Year: 1973
Tongue: French
Weight: 98 KB
Volume: 14
Category: Article
ISSN: 0040-4039
DOI: 10.1016/s0040-4039(01)96311-7

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Synthesis and antiinflammatory activity

Synthesis and antiinflammatory activity of 9-thiabicyclo[3.3.1]nonane derivatives

✍ G. A. Tolstikov; V. P. Krivonogov; B. I. Galimov; D. N. Lazareva; V. A. Davydova 📂 Article 📅 1997 🏛 Springer 🌐 English ⚖ 421 KB

An aberrant acetylation of 9-thiabicyclo

An aberrant acetylation of 9-thiabicyclo[3.3.1]nonan-2,6-dione

✍ Peter H. McCabe; William Routledge 📂 Article 📅 1973 🏛 Elsevier Science 🌐 French ⚖ 99 KB

ChemInform Abstract: Synthesis and Antii

ChemInform Abstract: Synthesis and Antiinflammatory Activity of 9-Thiabicyclo[3.3.1]nonane Derivatives.

✍ G. A. TOLSTIKOV; V. P. KRIVONOGOV; B. I. GALIMOV; D. N. LAZAREVA; V. A. DAVYDOVA 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 30 KB 👁 2 views

Antioxidant activity of some derivatives

Antioxidant activity of some derivatives of 9-thiabicyclo[3,3,1]nonane in rubber and rubber vulcanizates

✍ J.-M. Herdan; Liana Cira; Maria Giurginca; G. Ivan 📂 Article 📅 1992 🏛 Elsevier Science 🌐 English ⚖ 334 KB

ChemInform Abstract: 2,6-Dichloro-9-thia

ChemInform Abstract: 2,6-Dichloro-9-thiabicyclo[3.3.1]nonane: A Privileged, Bivalent Scaffold for the Display of Nucleophilic Components.

✍ Antonella Converso; Kristina Burow; Andreas Marzinzik; K. Barry Sharpless; M. G. 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 33 KB 👁 1 views

Preparation and reactions of 1,5-polymet

Preparation and reactions of 1,5-polymethylene-bridged 3,7-dimethylenebicyclo[3.3.1]nonan-9-ones

✍ T. Mori; K. Kimoto; M. Kawanisi; H. Nozaki 📂 Article 📅 1969 🏛 Elsevier Science 🌐 French ⚖ 222 KB

During a synthetic work on &&-muscone (11, we have investigated the condensation reaction of cycloalkanones I and d,d-dlchlorolsobutylene to flnd out that this reaction provides substantial amounts of the tltle oompounds II in addltlon to the deslred blcycllc products. The current lntereet in bloyol