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Lithium aluminum hydride–Aluminum chloride

氢化铝 氢解 科学网 锂(药物) 引用 化学 图书馆学 计算机科学 心理学 有机化学 生物化学 精神科 催化作用 甲醇 梅德林
作者
Tse‐Lok Ho,Mary Fieser,Louis Fieser
出处
期刊:Fieser and Fieser's Reagents for Organic Synthesis 被引量:1
标识
DOI:10.1002/9780471264194.fos06258
摘要

Lithium aluminum hydride–Aluminum chloride Tse-Lok Ho, Tse-Lok HoSearch for more papers by this authorMary Fieser, Mary FieserSearch for more papers by this authorLouis Fieser, Louis FieserSearch for more papers by this author Tse-Lok Ho, Tse-Lok HoSearch for more papers by this authorMary Fieser, Mary FieserSearch for more papers by this authorLouis Fieser, Louis FieserSearch for more papers by this author First published: 15 December 2006 https://doi.org/10.1002/9780471264194.fos06258Citations: 1 Read the full textAbout ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat No abstract is available for this article. Bibliography 1 W. J. Bailey and F. Marktscheffel, J. Org., 25, 1797 (1960) 10.1021/jo01080a032 CASWeb of Science®Google Scholar 2 B. R. Brown, J. Chem. Soc., 2756 (1952). 10.1039/jr9520002756 CASWeb of Science®Google Scholar For other examples of hydrogenolysis see A. J. Birch and M. Slaytor, Chem. Ind., 1524 (1956). Web of Science®Google Scholar 3 J. Broome, B. R. Brown, A. Roberts, and A, M.S. White, J. Chem. Soc., 1406 (1960) 10.1039/jr9600001406 Web of Science®Google Scholar 4 W. G. Dauben and J. F. Eastham, Am. Soc., 73, 3260 (1951) 10.1021/ja01151a078 CASWeb of Science®Google Scholar 5 R. F. Nystrom and C. R. A. Berger, Am. Soc., 80, 2896 (1958); 10.1021/ja01544a075 CASWeb of Science®Google Scholar B. R. Brown and A. M. S. White, J. Chem. Soc., 3755 (1957); 10.1039/jr9570003755 CASWeb of Science®Google Scholar J. Blackwell and W. J. 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Soc., 80, 1744 (1958); 10.1021/ja01540a060 CASWeb of Science®Google Scholar E. L. Eliel and M. N. Rerick, ibid., 82, 1362 (1960); Web of Science®Google Scholar M. N. Rerick and E. L. Eliel, ibid., 84, 2356 (1962) Web of Science®Google Scholar 15 R. F. Nystrom, Am. Soc., 77, 2544 (1955) 10.1021/ja01614a053 CASGoogle Scholar 16 R. F. Nystrom, Am. Soc., 81, 610 (1959) 10.1021/ja01512a026 CASWeb of Science®Google Scholar 17 M. N. Rerick et al., Tetrahedron Letters, 629 (1963) Web of Science®Google Scholar 18Change to read: R. A. Daignault and E. L. Eliel, Org. Syn., 47, 37 (1967) 10.15227/orgsyn.047.0037 CASGoogle Scholar 19Change to read: E. L. Eliel, R. J. L. Martin, and D. Nasipuri, ibid., 47, 16 (1967) Google Scholar 20 J. E. Bridgeman, E. R. H. Jones, G. D. Meakins, and J. Wicha, Chem. Commun., 898 (1967) Web of Science®Google Scholar 21 M. Fetizon, J.-C. Gramain, and I. Hanna, Compt. Rend. (C), 929 (1967) Web of Science®Google Scholar 22 E. C. Ashby and J. Prather, Am. Soc., 88, 729 (1966) 10.1021/ja00956a021 CASWeb of Science®Google Scholar 23 N. O. V. Sonntag, S. Linder, E. I. Becker, and P. E. Spoerri, Am. Soc., 75, 2283 (1953) 10.1021/ja01106a001 CASWeb of Science®Google Scholar 24 M. P. Cava and K. Narasimhan, J. Org., 34, 3641 (1969) 10.1021/jo01263a097 CASWeb of Science®Google Scholar 25 R. A. Sauers, W. Schinski, M. M. Mason, E. O'Hara, and B. Byrne, J. Org., 38, 642 (1973). 10.1021/jo00944a005 CASWeb of Science®Google Scholar 26 W. J. Gensler, J. J. Langone, and M. B. Floyd, Am. Soc., 93, 3828 (1971). 10.1021/ja00744a079 CASWeb of Science®Google Scholar 27Obtained by treatment of 4-octyne with ethyl diazoacetate in ether. Google Scholar 28 A. Romeo and M. P. Paradisi, J. Org., 37, 46 (1972). 10.1021/jo00966a012 CASPubMedWeb of Science®Google Scholar 29 D. C. Wigfield and K. Taymaz, Tetrahedron Letters, 4841 (1973). 10.1016/S0040-4039(01)87351-2 Web of Science®Google Scholar 30 M. J. Jorgenson, ibid., 559 (1962). Web of Science®Google Scholar 31 B. R. Brown and A. M. S. White, J. Chem. Soc., 3755 (1957). 10.1039/jr9570003755 CASWeb of Science®Google Scholar 32 W. G. Dauben, R. G. Williams, and R. D. McKelvey, Am. Soc., 95, 3932 (1973). 10.1021/ja00793a018 CASPubMedWeb of Science®Google Scholar 33 R. M. Pagni and C. R. Watson, Jr., Tetrahedron, 29, 3807 (1973). 10.1016/0040-4020(73)80198-X CASWeb of Science®Google Scholar 34 A. H. Albert, G. R. Pettit, and P. Brown, J. Org., 38, 2197 (1973). 10.1021/jo00952a018 CASWeb of Science®Google Scholar 35 W. E. Fristad, T. R. Baily, and L. A. Paquette, J. Org., 43, 1620 (1978). 10.1021/jo00402a043 CASWeb of Science®Google Scholar 36 J. J. Eisch and J. T. Trainor, ibid., 28, 487, 2870 (1963); Web of Science®Google Scholar C. M. Robbins and G. H. Whitham, J.C.S. Chem. Comm., 697 (1976). 10.1039/C39760000697 Web of Science®Google Scholar 37 A. Borbas, J. Hajko, M. Kajtar-Peredy, and A. Liptak, JCC 12, 191 (1993). Web of Science®Google Scholar 38 S. Nagahara, K. Maruoka, and H. Yamamoto, BCSJ 66, 3783 (1993). 10.1246/bcsj.66.3783 CASWeb of Science®Google Scholar Citing Literature Fieser and Fieser's Reagents for Organic SynthesisBrowse other articles of this reference work:BROWSE A-Z ReferencesRelatedInformation

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