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Derivatives of phosphorus acids and 2-chloro-2-propen-1-ol

✍ Scribed by B. A. Arbuzov; V. M. Zoroastrova; N. D. Ibragimova; I. D. Neklesova; B. L. Mazur; M. A. Kudrina; N. V. Egorova; I. S. Iraidova

Book ID: 112433998
Publisher: Springer
Year: 1967
Tongue: English
Weight: 494 KB
Volume: 16
Category: Article
ISSN: 1573-9171
DOI: 10.1007/bf00908279

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📜 SIMILAR VOLUMES

New reactivity of 1-(2-pyridyl)-2-propen

New reactivity of 1-(2-pyridyl)-2-propen-1-ol with nitro derivatives

✍ Donatella Giomi; Renzo Alfini; Alberto Brandi 📂 Article 📅 2008 🏛 Elsevier Science 🌐 French ⚖ 164 KB

Dehydrochlorination of 3-Chloro-2-propen

Dehydrochlorination of 3-Chloro-2-propen-1-ol: Preparation of Propargyl Alcohol 1

✍ Hatch, Lewis F.; Moore, Allen C. 📂 Article 📅 1944 🏛 American Chemical Society 🌐 English ⚖ 380 KB

Synthesis and reactions of 2-nitro-1-pro

Synthesis and reactions of 2-nitro-1-propen-3-ol

✍ G. V. Oreshko; L. T. Eremenko 📂 Article 📅 1989 🏛 Springer 🌐 English ⚖ 322 KB

(Z)-2,3-Bis(3,4-dimethoxyphenyl)-2-pro

(Z)-2,3-Bis(3,4-dimethoxyphenyl)-2-propen-1-ol

✍ Stomberg, Rolf ;Albinsson, Bo ;Langer, Vratislav ;Li, Shiming ;Lundquist, Knut 📂 Article 📅 2004 🏛 International Union of Crystallography 🌐 English ⚖ 239 KB

Single-crystal X-ray study T = 295 K Mean '(C±C) = 0.003 A Ê R factor = 0.034 wR factor = 0.107 Data-to-parameter ratio = 12.2 For details of how these key indicators were automatically derived from the article, see http://journals.iucr.org/e.

ChemInform Abstract: Synthesis of 1,2-Di

ChemInform Abstract: Synthesis of 1,2-Dihydroxyindolizidines from 1-(2-Pyridyl)-2-propen-1-ol.

✍ Donatella Giomi; Renzo Alfini; Alessandra Micoli; Elisa Calamai; Cristina Faggi; 📂 Article 📅 2012 🏛 John Wiley and Sons ⚖ 30 KB 👁 1 views

The fragmentation of 1-phenyl-2-propen-1

The fragmentation of 1-phenyl-2-propen-1-ol under electron impact

✍ Jean-Pierre Denhez; Madeleine Corval; Pierre Dizabo 📂 Article 📅 1981 🏛 John Wiley and Sons 🌐 English ⚖ 409 KB

## Abstract The electron impact mass spectra of 1‐phenyl‐2‐propen‐1‐ol and its specifically deuterated analogues have been investigated. Most of the decomposition pathways involve skeletal rearrangements or hydrogen atom transfers, such that a rearrangement of the excited molecular ions of 1‐phenyl