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Reakcja Mitsunobu (Polish Wikipedia)

Analysis of information sources in references of the Wikipedia article "Reakcja Mitsunobu" in Polish language version.

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  • publikacja w otwartym dostępie – możesz ją przeczytać Mitsunobu Oyo, Yamada Masaaki. Preparation of Esters of Carboxylic and Phosphoric Acid via Quaternary Phosphonium Salts. „Bull. Chem. Soc. Japan”. 40 (10), s. 2380-2382, 1967. DOI: 10.1246/bcsj.40.2380. 
  • publikacja w otwartym dostępie – możesz ją przeczytać Mitsunobu Oyo, Yamada Masaaki, Teruaki Mukaiyama. Preparation of Esters of Phosphoric Acid by the Reaction of Trivalent Phosphorus Compounds with Diethyl Azodicarboxylate in the Presence of Alcohols. „Bull. Chem. Soc. Japan”. 40 (4), s. 935, 1967. DOI: 10.1246/bcsj.40.935. 
  • Oyo Mitsunobu. The Use of Diethyl Azodicarboxylate and Triphenylphosphine in Synthesis and Transformation of Natural-Products. „Synthesis”, s. 1-28, 1981. DOI: 10.1055/s-1981-29317. 
  • D. L. Hughes. Progress in the Mitsunobu reaction. A review. „Org. Prep.”. 28 (2), s. 127-164, 1996. DOI: 10.1080/00304949609356516. 
  • K. C. Kumara Swamy, N. N. Bhuvan Kumar, E. Balaraman, K. V. P. Pavan Kumar. Mitsunobu and Related Reactions: Advances and Applications. „Chem. Rev.”. 109 (6), s. 2551-2651, 2009. DOI: 10.1021/cr800278z. 
  • Edward Grochowski, Bruce D. Hilton, Robert J. Kupper, Christopher J. Michejda. Mechanism of the triphenylphosphine and diethyl azodicarboxylate induced dehydration reactions (Mitsunobu reaction). The central role of pentavalent phosphorus intermediates. „J. Am. Chem. Soc.”. 104 (24), s. 6876-6877, 1982. DOI: 10.1021/ja00388a110. 
  • David Camp, Ian D. Jenkins. The mechanism of the Mitsunobu esterification reaction. Part I. The involvement of phosphoranes and oxyphosphonium salts. „J. Org. Chem.”. 54 (13), s. 3045-3049, 1989. DOI: 10.1021/jo00274a016. 
  • David Camp, Ian D. Jenkins. The mechanism of the Mitsunobu esterification reaction. Part II. The involvement of (acyloxy)alkoxyphosphoranes. „J. Org. Chem.”. 54 (13), s. 3049-3054, 1989. DOI: 10.1021/jo00274a017. 
  • Chuljin Ahn, Reuben Correia, Philip DeShong. Mechanistic Study of the Mitsunobu Reaction. „J. Org. Chem.”. 67 (6), s. 1751–1753, 2002. DOI: 10.1021/jo001590m. 
  • Stephen F. Martin, Jeffrey A. Dodge. Efficacious modification of the mitsunobu reaction for inversions of sterically hindered secondary alcohols. „Tetrahedron Letters”. 32 (26), s. 3017-3020, 1991. DOI: 10.1016/0040-4039(91)80675-V. 
  • D. L. Hughes, R. A. Reamer, J. J. Bergan, E. J. J. Grabowski. A mechanistic study of the Mitsunobu esterification reaction. „J. Am. Chem. Soc.”. 110 (19), s. 6487–6491, 1988. DOI: 10.1021/ja00227a032. 
  • R. P. Volante. A mechanistic study of the Mitsunobu esterification reaction. „Tetrahedron Letters”. 22 (33), s. 3119-3122, 1981. DOI: 10.1016/S0040-4039(01)81842-6. 
  • Tarek Sammakia, Jon S. Jacobs. Picolinic acid as a partner in the Mitsunobu reaction: Subsequent hydrolysis of picolinate esters under essentially neutral conditions with copper acetate in methanol. „Tetrahedron Letters”. 40 (14), s. 2685-2688, 1999. DOI: 10.1016/S0040-4039(99)00332-9. 
  • S. Ito. Development of new synthetic reagents in Mitsunobu-type reaction. „Yakugaku Zasshi-Journal of the Pharmaceutical Society of Japan”. 121 (8), s. 567-583, 2001. DOI: 10.1248/yakushi.121.567. (ang.). 
  • R. Dembinski. Recent advances in the Mitsunobu reaction: Modified reagents and the quest for chromatography-free separation. „Eur.J.Org.Chem.”, s. 2763-2772, 2004. DOI: 10.1002/ejoc.200400003. (ang.). 
  • T. Y. S. But, P. H. Toy. The Mitsunobu reaction: Origin, mechanism, improvements, and applications. „Chemistry-An Asian Journal”. 2 (11), s. 1340-1355, 2007. DOI: 10.1002/asia.200700182. 
  • K. C. K. Swamy, N. N. B. Kumar, E. Balaraman, K. V. P. P. Kumar. Mitsunobu and Related Reactions: Advances and Applications. „Chem.Rev.”. 109 (6), s. 2551-2651, 2009. DOI: 10.1021/cr800278z. (ang.). 
  • A. J. Reynolds, M. Kassiou. Recent Advances in the Mitsunobu Reaction: Modifications and Applications to Biologically Active Molecules. „Curr.Org.Chem.”. 13 (16), s. 1610-1632, 2009. DOI: 10.2174/138527209789578144. (ang.). 
  • Tetsuto Tsunoda, Chisato Nagino, Miwa Oguri, Shô Itô. Mitsunobu-type alkylation with active methine compounds. „Tetrahedron Letters”. 37 (14), s. 2459-2462, 1996. DOI: 10.1016/0040-4039(96)00318-8. 
  • Tetsuto Tsunoda, Yoshiko Yamamiya, Shô Itô. 1,1'-(azodicarbonyl)dipiperidine-tributylphosphine, a new reagent system for mitsunobu reaction. „Tetrahedron Letters”. 34 (10), s. 1639-1642, 1993. DOI: 10.1016/0040-4039(93)85029-V. 
  • Tetsuto Tsunoda, Junko Otsuka, Yoshiko Yamamiya, Shô Itô. N,N,N',N'-Tetramethylazodicarboxamide (TMAD), A New Versatile Reagent for Mitsunobu Reaction. Its Application to Synthesis of Secondary Amines. „Chemistry Letters”. 23 (3), s. 539, 1994. DOI: 10.1246/cl.1994.539. 
  • Tetsuto Tsunoda, Yumi Kawamura, Kaori Uemoto, Shô Itô. Mitsunobu Type C-N Bond Formation with 4,7-Dimethyl-3,5,7-hexahydro-1,2,4,7-tetrazocin-3,8-dione(DHTD), a New Cyclic Azodicarboxamide. „Heterocycles”. 47 (1), s. 177-179, 1997. DOI: 10.3987/COM-97-S(N)78. 
  • Mark von Itzstein, Mauro Mocerino. (p-Dimethylaminophenyl) Diphenylphosphine: A More Practical Phosphine in the Mitsunobu Reaction. „Synthetic Communications”. 20 (13), s. 2049-2057, 1990. DOI: 10.1080/00397919008053136. 
  • Ian A. O'Neil, Stephen Thompson, Clare L. Murray, S. Barret Kalindjian. DPPE: A convenient replacement for triphynylphosphine in the staudinger and Mitsunobu reactions. „Tetrahedron Letters”. 39 (42), s. 7787-7790, 1998. DOI: 10.1016/S0040-4039(98)01702-X. 
  • Jeffrey C. Pelletier, Scott Kincaid. Mitsunobu reaction modifications allowing product isolation without chromatography: application to a small parallel library. „Tetrahedron Letters”. 41 (6), s. 797-800, 2000. DOI: 10.1016/S0040-4039(99)02214-5. 
  • Anthony G. M. Barrett, Richard S. Roberts, Jurgen Schroder. Impurity Annihilation: Chromatography-Free Parallel Mitsunobu Reactions. „Org. Lett.”. 2 (19), s. 2999-3001, 2000. DOI: 10.1021/ol006313g. 
  • Bruce H. Lipshutz, David W. Chung, Brian Rich, Ricardo Corral. Simplification of the Mitsunobu Reaction. Di-p-chlorobenzyl Azodicarboxylate: A New Azodicarboxylate. „Org. Lett.”. 8 (22), s. 5069–5072, 2006. DOI: 10.1021/ol0618757. 
  • Stanislaw Czernecki, Jean-Marc Valéry. An Efficient Synthesis of 3′-Azido-3′-deoxythymidine (AZT). „Synthesis”, s. 239-240, 1991. DOI: 10.1055/s-1991-26434. 

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  • Louis S. Hegedus, Michael S. Holden, James M. McKearin, cis-N-tosyl-3-methyl-2-azabicyclo[3.3.0]oct-3-ene, „Organic Syntheses”, 62, 1990, s. 48, DOI: 10.15227/orgsyn.062.0048.
  • Wataru Kurosawa, Toshiyuki Kan, Tohru Fukuyama, Preparation of secondary amines from primary amines via 2-nitrobenzenesulfonamides: N-(4-methoxybenzyl)-3-phenylpropylamine, „Organic Syntheses”, 79, s. 186, DOI: 10.15227/orgsyn.079.0186.