By Thomas T. Tidwell
The main up to date unmarried reference on ketene chemistry for the practising researcherKetenes are valued via either practising natural man made chemists and pharmaceutical researchers for his or her ease of training, excessive reactivity, and flexibility of use.Ketenes, moment variation is an up to date model of the finest source in this very important category of compounds, and contours a accomplished, self-contained advisor to all elements of ketene chemistry, including:* forms of ketenes* Theoretical reviews* Thermochemistry* Ketene coaching* Reactions, together with mechanisms and artificial purposes* Spectroscopy and actual propertiesWhile conserving a lot of the very important info awarded within the unique textual content, the second one version covers all advances made of 1995 to the current, together with updates from the literature; over 1,000 new references; and new sections on cycloaddition reactions, ketenes from esters, ketene reactions utilizing polymer helps, and oxoquinone methides.
Read Online or Download Ketenes PDF
Best organic books
Catalyzed Carbon-Heteroatom Bond Formation
Written by way of an skilled editor commonly acclaimed in the clinical neighborhood, this e-book covers every thing from oxygen to nitrogen functionalities. From the contents: Palladium-Catalyzed Syntheses of 5-membered Saturated Heterocycles The Formation of Carbon-Sulfur and Carbon-Selenium Bonds through Substitution and Addition Reactions Catalyzed via Transition steel Complexes Palladium-Catalysis for Oxidative 1,2-Difunctionalization of Alkenes Palladium-Catalyzed Formation of fragrant Heterocycles Rhodium-Catalyzed Amination of C-H-Bonds Transition Metal-Catalyzed Synthesis of Heterocycles Copper-Catalyzed Synthesis of Azoles Palladium(II)-Catalyzed C-N Bond Formation related to Aminopalladation of Aklenes Carbon-Heteroatom Bond Formation via Rh(I)-Catalyzed Ring-Opening Reactions fresh Advances in Homogeneous Gold Catalysis: Formation of Carbon-Heteroatom Bonds the result's an critical resource of data for the strategic making plans of the unreal routes for natural, catalytic and medicinal chemists, in addition to chemists in undefined.
The 1st name during this zone in lots of years, this name brings jointly the entire parts of curiosity in natural reactions related to carbocations in a single convenient quantity. It covers new parts equivalent to nuclear decay iteration, artificial functions and NMR observations. additionally incorporated is wide and distinct insurance of theoretical and gasoline section facts.
Advances in Heterocyclic Chemistry
Content material: Microwave irradiation for accelerating natural reactions. half I: Three-, 4- and 5-membered heterocycles / E S H El Ashry, E Ramadan, AA Kassem, M Hagar -- Organometallic complexes of the n²(N, C)-coordinated derivatives of pyridine / Alexander Sadimenko -- Annulated heterocyclo-purines II: fused six- and more-membered heterocyclo-purinediones, -purinones and -purineimines / Alfonz Rybar -- Flourine-containing heterocycles.
Chromium Oxidations in Organic Chemistry
Chromium oxidation, popular and commonly explored in natural chemistry because the very starting of this technology, is a subject of present curiosity for the natural chemist as evidenced via the continual improvement of latest techni ques and approaches suggested within the literature. Chromium oxidation is a straightforward strategy which are simply played within the laboratory and scaled up in to boot.
- Thiophene and Its Derivatives, Part 3 (The Chemistry of Heterocyclic Compounds, Vol. 44)
- Synthon Model of Organic Chemistry and Synthesis Design
- Biomimetic and Bioorganic Chemistry, 1st Edition
- Microwaves in organic synthesis Vol. 2, Edition: 2., completely revised and enl. ed
- Gravity-Driven Water Flow in Networks: Theory and Design
- Handbook of Bond Dissociation Energies in Organic Compounds
Additional resources for Ketenes
Example text
J. 1999, 5, 24–28. 29. Allen, A. ; Fenwick, M. ; Missiha, S. ; Tidwell, T. T. Org. Lett. 1999, 1, 693–696. 30. Russell, D. ; Wesendrup, R. J. Chem. Phys. 2002, 117, 5252–5256. 31. ; Seppelt, K. Chem. Ber. 1990, 123, 2187–2190. 32. ; Allouche, A. Chem. Phys. 1991, 150, 395–403. 33. Gerry, M. C. ; Westwood, N. P. C. Can. J. Chem. 1985, 63, 676–677. 34. Mal’tsev, A. ; Zuev, P. ; Nefedov, O. M. Izv. Akad. Nauk SSSR, Ser. Khim. 1985, 957–958. Engl. Transl. 1985, 876. 35. ; Hori, T. Bull. Chem. Soc. Jpn.
10. Allen, A. , University of Toronto, unpublished results. 11. Nadzhimutdinov, S. ; Slovokhotova, N. ; Kargin, V. A. Zh. Fiz. Khim. 1966, 40, 893–897. Chem. Abstr. 1966, 65, 4851h. 12. ; Feiler, L. ; Otto, P. Chem. Ber. 1969, 102, 3444–3459. INFRARED SPECTRA AND RAMAN SPECTRA 39 13. ; Hori, T. Bull. Chem. Soc. Jpn. 1983, 56, 171–174. 14. Winnik, M. ; Masuhara, H. J. Am. Chem. Soc. 1991, 113, 9702–9704. 15. Hobson, J. ; Al Holly, M. ; Malpass, J. R. Chem. Commun. 1968, 764–766. 16. ; Allen, A. ; Tidwell, T.
C. ; Westwood, N. P. C. J. Chem. Phys. 1983, 79, 4655–4663. ; Christiansen, J. ; Rastrup-Andersen, J. J. Chem. Phys. 1966, 45, 883–887. Westwood, N. P. ; Gerry, M. C. L. J. Mol. Spectrosc. 1989, 136, 93–104. Brown, R. ; Godfrey, P. ; Woodruff, M. Aust. J. Chem. 1979, 32, 2103–2109. Nair, K. P. ; Rudolph, H. ; Dreizler, H. J. Mol. Spectrosc. 1973, 48, 571–591. Gerry, M. C. ; Westwood, N. P. C. Can. J. Chem. 1985, 63, 676–677. ; Khabashesku, V. ; Kagramanov, N. ; Nefedov, O. M. J. Am. Chem. Soc. 1989, 111, 2845-2849.