Small ring compounds in organic synthesis / Vol. 2

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Rate this product. Please log In to rate. Also Recommended. Asian Journal of Oncology. Veterinary and Comparative Orthopaedics and Traumatology. Get NEWS! Product Search. Publishing Ltd. Tardy, Jr. Select Year Half of an n-hexane molecule is distorted trigonal-bipyramidal geometry. The NHC ligands in omitted for clarity. The Si C bond lengths in 2 1. The differences in Si Cl bond lengths for 2 The Si Cl distances in 2 and 3 are noticeably different and shorter than the average bond length bond lengths in 2 1.

The Si O bonds in 2 1. The three-membered strained rings in 2 and 3 3 1. It negative chlorine atoms at the silicon atom. KGaA, Weinheim www. The chlorine atoms in 5 occupy one axial Cl2 and one equatorial position Cl1 , and as expected their bond lengths differ significantly axial 2.

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The oxygen atoms of the planar five-membered ring chelate axial and equatorial positions. In summary, we have reported for the first time a convenient method for the preparation of stable silaoxiranes Figure 3. Molecular structure of 4; anisotropic displacement parame- by the reaction of silylenes with ketones. Two toluene molecules are stable compounds and were fully characterized. They are the omitted for clarity. They may serve Their formation proves that base stabili- zation allows isolation of silaoxiranes which are otherwise spirocyclic structure the Si atom is part of a four- and a three- assumed to exist only as intermediates.

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The Si atom exhibits a distorted square- pyramidal geometry. The coordination sites of the Si atom are Received: February 10, occupied by the N atoms of the amidinato ligand and one Published online: April 15, oxygen and one carbon atom from the epoxide ring. The fifth coordination site is occupied by a chlorine atom.

The Si O and Si C distances of 1. The Si Cl distance of 2. Hodgson, C. Adolfsson, D. Nielsen, E. Crotti, M.

Bicyclic compounds - Alkanes, cycloalkanes, and functional groups - Organic chemistry - Khan Academy

Olofsson, P. Fokin, P. Gaspar, R. Rappoport, Y. Apeloig , Wiley, New York, , pp.

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Haff, T. Schmedake, R. West, Acc. Hill, R. West, J. Gehr- hus, P. Hitchcock, R.

Small Ring Compounds in Organic Synthesis VI | Armin de Meijere | Springer

Pongtavornpinyo, L. Zhang, J. Dalton Trans. Benson, Thermochemical Kinetics, 2nd ed. Molecular structure of 5; anisotropic displacement parame- York, , pp. Driess, H. The second molecule is omitted for Chem. Si1 O2 1.

Small Ring Compounds in Organic Synthesis VI

Ishikawa, K. Nishimura, H. Sugisawa, M. Kumada, J. Ishikawa, H. O2-Si1-O1 Fuchikami, M. Kumada, T. Yamabe, H. Kawakami, Cl2 Fukui, Y. Ueki, H. Shizuka, J. Matsui, K. Hirotsu, Organometallics , 1, — , , — ; l S. Calad, K.

Small Ring Compounds in Organic Synthesis VI

Woerpel, Org. Seyferth, M. Shannon, S. Vick, T. Lim, , 9, — ; m B. Howard, K. Organometallics , 4, 57 — 62; e M. Ishikawa, T. Horio, Y.


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Kunai, T. Tsukihara, H. Naitou, Organometallics , 10, — ; o M. Woerpel, J. Kunai, Y. Matsuo, J. Ohshita, M. Ishikawa, Y. Aso, T. Otsubo, F. Ogura, Organometallics , 14, [8] a P. Jutzi, D. Eikenberg, E. Bunte, A. Neumann, — ; g W.

Ando, T. Shiba, T. Hidaka, K. Description This current and five previous volumes Volumes , , , , convincingly demonstrate the vast applications of small rings in modern Organic Synthesis. Such applications range from total syntheses of cyclopropyl-group-containing natural products and non-natural biologically active compounds or compounds with other important properties via syntheses of cyclopropyl analogues to the use of cyclopropyl groups as reactive subunits.

This volume covers a survey of the wide range of biological activities of cyclopropyl-containing compounds, up-to-date comprehensive reviews on the multiple applicabilities of two multifunctional small ring building blocks - methyl 2-chlorocyclopropylideneacetate and bicyclopropylidene - in Organic Synthesis as well as a striking new approach to cyclopentenones from easily accessible 1-ethynylcyclopropanols, which is rather general and favorably complements other cyclopentenone syntheses. Product details Format Hardback pages Dimensions x x Other books in this series. Add to basket. Cyclic Compounds Friedrich L.

Triplet States I Kendall N. Microfluidics Bingcheng Lin. Polymer Mechanochemistry Roman Boulatov. Hydroformylation for Organic Synthesis Maurizio Taddei. Density Functionals Erin R. Asymmetric Organocatalysis Benjamin List. Pyrethroids Noritada Matsuo. Nonaqueous Chemistry Kendall N. Back cover copy This current and five previous volumes Volumes , , , , convincingly demonstrate the vast applications of small rings in modern Organic Synthesis.



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