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NTIS 바로가기Chemistry letters, v.20 no.1, 1991년, pp.43 - 46
Tomooka, Katsuhiko (Department of Chemical Technology, Tokyo Institute of Technology) , Wei, Shih-Yi (Department of Chemical Technology, Tokyo Institute of Technology) , Nakai, Takeshi (Department of Chemical Technology, Tokyo Institute of Technology)
The E/Z stereoselection in the acyclic oxy-Cope rearrangement of stereochemically-defined 3-methyl-1,5-heptadien-4-ols, prepared via diastereoselective [2,3]Wittig variants, has been evaluated, thereby permitting to propose a reasonable transition-state model for this type of anionic oxy-Cope varian...
Lee, Eun, Shin, In Jae, Kim, Tae Seong. Enantiocontrolled synthesis of quaternary carbon centers via anionic oxy-Cope rearrangement: an efficient synthesis of (+)-dihydromayurone. Journal of the American Chemical Society, vol.112, no.1, 260-264.
Paquette, Leo A., Teleha, Christopher A., Taylor, Richard T., Maynard, George D., Rogers, Robin D., Gallucci, Judith C., Springer, James P.. Boat/chair topographic stereoselection during anionic oxy-Cope rearrangement of 1-alkenyl-2-cyclopentenyl-endo-norbornan-2-ols. Journal of the American Chemical Society, vol.112, no.1, 265-277.
Paquette, Leo A., Pegg, Neil A., Toops, Dana, Maynard, George D., Rogers, Robin D.. [3.3] Sigmatropy within 1-vinyl-2-alkenyl-7,7-dimethyl-exo-norbornan-2-ols. The first atropselective oxyanionic Cope rearrangement. Journal of the American Chemical Society, vol.112, no.1, 277-283.
Mikami, K., Taya, S., Nakai, T., Fujita, Y.. New sigmatropic sequences based on the [2,3] Wittig rearrangement of bis(allylic) ethers. Regiocontrolled joining reactions of two or three allylic moieties leading to unsaturated carbonyl compounds. Journal of organic chemistry, vol.46, no.26, 5447-5449.
Mikami, K., Kishi, N., Nakai, T., Fujita, Y.. New sigmatropic sequences based on the [2,3]-wittig rearrangement of the bis-allylic ether system - A general approach to regiocontrolled c-c bond formation of allylic moieties leading to unsaturated carbonyl compounds. Tetrahedron, vol.42, no.11, 2911-2918.
Nakai, Takeshi, Mikami, Koichi. [2,3]-Wittig sigmatropic rearrangements in organic synthesis. Chemical reviews, vol.86, no.5, 885-902.
Mikami, K., Azuma, K.-I., Nakai, T.. [2,3]-Wittig sigmatropic rearrangement of crotyl propargyl ether system. An emerging tool for control of acyclic stereochemistry. Tetrahedron, vol.40, no.12, 2303-2308.
Evans, D. A., Golob, A. M.. [3,3]Sigmatropic rearrangements of 1,5-diene alkoxides. Powerful accelerating effects of the alkoxide substituent. Journal of the American Chemical Society, vol.97, no.16, 4765-4766.
Evans, David A., Nelson, John V.. Stereochemical study of the [3,3] sigmatropic rearrangement of 1,5-diene-3-alkoxides. Application to the stereoselective synthesis of (.+-.)-juvabione. Journal of the American Chemical Society, vol.102, no.2, 774-782.
Thies, Richard W., Wills, Max T., Chin, Alice W., Schick, Lawrence E., Walton, Edward S.. Siloxy-Cope and oxy-Cope rearrangements of the cis-1-vinylcyclooct-3-en-1-ol system. Journal of the American Chemical Society, vol.95, no.16, 5281-5285.
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