Journal articles on the topic 'Mitsunobu reaction'
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Panday, Sharad Kumar. "Advances in the Mitsunobu Reaction: An Excellent Organic Protocol with Versatile Applications." Mini-Reviews in Organic Chemistry 16, no. 2 (January 4, 2019): 127–40. http://dx.doi.org/10.2174/1570193x15666180612090313.
Full textToy, P., and T. But. "Catalytic Mitsunobu Reaction." Synfacts 2006, no. 9 (September 2006): 0947. http://dx.doi.org/10.1055/s-2006-949230.
Full textHain, Julia, Patrick Rollin, Werner Klaffke, and Thisbe K. Lindhorst. "Anomeric modification of carbohydrates using the Mitsunobu reaction." Beilstein Journal of Organic Chemistry 14 (June 29, 2018): 1619–36. http://dx.doi.org/10.3762/bjoc.14.138.
Full textKasama, Kengo. "Redox-neutral Mitsunobu Reaction." Journal of Synthetic Organic Chemistry, Japan 79, no. 4 (April 1, 2021): 344–45. http://dx.doi.org/10.5059/yukigoseikyokaishi.79.344.
Full textLongwitz, Lars, and Thomas Werner. "The Mitsunobu reaction, reimagined." Science 365, no. 6456 (August 29, 2019): 866–67. http://dx.doi.org/10.1126/science.aay6635.
Full textBoyle, Benjamin T., Kyle G. Nottingham, and Andrew McNally. "An Organocatalytic Mitsunobu Reaction." Trends in Chemistry 2, no. 2 (February 2020): 174–75. http://dx.doi.org/10.1016/j.trechm.2019.11.001.
Full textMunawar, Saba, Ameer Fawad Zahoor, Shafaqat Ali, Sadia Javed, Muhammad Irfan, Ali Irfan, Katarzyna Kotwica-Mojzych, and Mariusz Mojzych. "Mitsunobu Reaction: A Powerful Tool for the Synthesis of Natural Products: A Review." Molecules 27, no. 20 (October 17, 2022): 6953. http://dx.doi.org/10.3390/molecules27206953.
Full textJia, Zhaozhong J., Sandra Kelberlau, Lars Olsson, G. Anilkumar, and Bert Fraser-Reid. "The Mitsunobu Reaction of Tetrachlorophthalimide." Synlett 1999, no. 5 (May 1999): 565–66. http://dx.doi.org/10.1055/s-1999-2680.
Full textMarkowicz, Marcin W., and Roman Dembinski. "Fluorous, Chromatography-Free Mitsunobu Reaction." Organic Letters 4, no. 22 (October 2002): 3785–87. http://dx.doi.org/10.1021/ol0264511.
Full textHUGHES, D. L. "ChemInform Abstract: The Mitsunobu Reaction." ChemInform 25, no. 44 (August 18, 2010): no. http://dx.doi.org/10.1002/chin.199444253.
Full textGrice, I. Darren, Peta J. Harvey, Ian D. Jenkins, Michael J. Gallagher, and Millagahamada G. Ranasinghe. "Phosphitylation via the Mitsunobu reaction." Tetrahedron Letters 37, no. 7 (February 1996): 1087–90. http://dx.doi.org/10.1016/0040-4039(95)02282-1.
Full textFletcher, S. "The Mitsunobu reaction in the 21st century." Organic Chemistry Frontiers 2, no. 6 (2015): 739–52. http://dx.doi.org/10.1039/c5qo00016e.
Full textCamp, D., and ID Jenkins. "The Reaction of Thiols and α,ω-Dithiols With Triphenylphosphine and Diisopropyl Azodicarboxylate." Australian Journal of Chemistry 43, no. 1 (1990): 161. http://dx.doi.org/10.1071/ch9900161.
Full textHarned, Andrew M., Helen Song He, Patrick H. Toy, Daniel L. Flynn, and Paul R. Hanson. "Multipolymer Solution-Phase Reactions: Application to the Mitsunobu Reaction." Journal of the American Chemical Society 127, no. 1 (January 2005): 52–53. http://dx.doi.org/10.1021/ja045188r.
Full textHuang, Yangen, Roger W. Read, and Xiaobei Wang. "Efficient Alkylation Methods for the Synthesis of Hybrid Fluorocarbon - Hydrocarbon Tetrazoles as Potential Fluorinated Surfactants." Australian Journal of Chemistry 63, no. 5 (2010): 802. http://dx.doi.org/10.1071/ch10005.
Full textSeio, Kohji, Munefumi Tokugawa, Kazuhei Kaneko, Takashi Shiozawa, and Yoshiaki Masaki. "A Systematic Study of the Synthesis of 2ʹ-Deoxynucleosides by Mitsunobu Reaction." Synlett 28, no. 15 (June 7, 2017): 2014–17. http://dx.doi.org/10.1055/s-0036-1588445.
Full textAhn, Chuljin, Reuben Correia, and Philip DeShong. "Mechanistic Study of the Mitsunobu Reaction." Journal of Organic Chemistry 68, no. 3 (February 2003): 1176. http://dx.doi.org/10.1021/jo027970k.
Full textYe, Xin-Shan, Jian Guo, Yu-Jiao Lu, and Li Zhang. "Hydrophobically Assisted Separation-Friendly Mitsunobu Reaction." Synlett 23, no. 11 (June 14, 2012): 1696–700. http://dx.doi.org/10.1055/s-0031-1290406.
Full textAhn, Chuljin, Reuben Correia, and Philip DeShong. "Mechanistic Study of the Mitsunobu Reaction." Journal of Organic Chemistry 67, no. 6 (March 2002): 1751–53. http://dx.doi.org/10.1021/jo001590m.
Full textManvar, Atul, and Anamik Shah. "Subtle Mitsunobu couplings under super-heating: the role of high-throughput continuous flow and microwave strategies." Org. Biomol. Chem. 12, no. 41 (2014): 8112–24. http://dx.doi.org/10.1039/c4ob01432d.
Full textBongarzone, S., A. Runser, C. Taddei, A. K. Haji Dheere, and A. D. Gee. "From [11C]CO2 to [11C]amides: a rapid one-pot synthesis via the Mitsunobu reaction." Chemical Communications 53, no. 38 (2017): 5334–37. http://dx.doi.org/10.1039/c7cc01407d.
Full textDai, Chuan, Jun Ma, Min Li, Wen Wu, Xuefeng Xia, and Jinqiang Zhang. "Diversity-oriented submonomer synthesis of azapeptides mediated by the Mitsunobu reaction." Organic Chemistry Frontiers 6, no. 14 (2019): 2529–33. http://dx.doi.org/10.1039/c9qo00296k.
Full textCamp, D., and ID Jenkins. "The Mechanism of the Mitsunobu Reaction. III. The Use of Tributylphosphine." Australian Journal of Chemistry 45, no. 1 (1992): 47. http://dx.doi.org/10.1071/ch9920047.
Full textTang, Xiaoping, Charlotte Chapman, Matthew Whiting, and Ross Denton. "Development of a redox-free Mitsunobu reaction exploiting phosphine oxides as precursors to dioxyphosphoranes." Chem. Commun. 50, no. 55 (2014): 7340–43. http://dx.doi.org/10.1039/c4cc02171a.
Full textAdler, Pauline, Antoine Fadel, Joëlle Prunet, and Nicolas Rabasso. "From acyclic to cyclic α-amino vinylphosphonates by using ring-closing metathesis." Organic & Biomolecular Chemistry 15, no. 2 (2017): 387–95. http://dx.doi.org/10.1039/c6ob02548j.
Full textMujahid, Mohammad, Jambu Subramanian, Viswanadh Nalla, Murugesan Sasikumar, Sunita Sharad Kunte, and Murugan Muthukrishnan. "A new and efficient enantioselective synthesis of both enantiomers of the calcium channel blocker bepridil." New Journal of Chemistry 41, no. 2 (2017): 824–29. http://dx.doi.org/10.1039/c6nj02928k.
Full textSugimoto, Osamu, Tomoyo Arakaki, Hiroka Kamio, and Ken-ichi Tanji. "The use of a Mitsunobu reagent for the formation of heterocycles: a simple method for the preparation of 3-alkyl-5-aryl-1,3,4-oxadiazol-2(3H)-ones from carboxylic acids." Chem. Commun. 50, no. 55 (2014): 7314–17. http://dx.doi.org/10.1039/c4cc01971g.
Full textPal, Pratik, Nandan Jana, and Samik Nanda. "Asymmetric total synthesis of paecilomycin E, 10′-epi-paecilomycin E and 6′-epi-cochliomycin C." Org. Biomol. Chem. 12, no. 41 (2014): 8257–74. http://dx.doi.org/10.1039/c4ob01400f.
Full textHolzer, Wolfgang, Brigitte Plagens, and Karin Lorenz. "Alkylation of Pyrazolones via the Mitsunobu Reaction." HETEROCYCLES 45, no. 2 (1997): 309. http://dx.doi.org/10.3987/com-96-7657.
Full textVarasi, Mario, Keith A. M. Walker, and Michael L. Maddox. "A revised mechanism for the Mitsunobu reaction." Journal of Organic Chemistry 52, no. 19 (September 1987): 4235–38. http://dx.doi.org/10.1021/jo00228a016.
Full textCamp, David, Graeme R. Hanson, and Ian D. Jenkins. "Formation of Radicals in the Mitsunobu Reaction." Journal of Organic Chemistry 60, no. 10 (May 1995): 2977–80. http://dx.doi.org/10.1021/jo00115a011.
Full textHughes, David L. "PROGRESS IN THE MITSUNOBU REACTION. A REVIEW." Organic Preparations and Procedures International 28, no. 2 (April 1996): 127–64. http://dx.doi.org/10.1080/00304949609356516.
Full textYoakim, Christiane, I. Guse, J. A. O’Meara, and B. Thavonekham. "Removable Phosphine Reagents for the Mitsunobu Reaction." Synlett, no. 4 (2003): 0473–76. http://dx.doi.org/10.1055/s-2003-37520.
Full textHuang, Hai, and Jun Yong Kang. "Mitsunobu Reaction Using Basic Amines as Pronucleophiles." Journal of Organic Chemistry 82, no. 13 (June 15, 2017): 6604–14. http://dx.doi.org/10.1021/acs.joc.7b00622.
Full textPokluda, Adam, Michal Kohout, Josef Chudoba, Martin Krupička, and Radek Cibulka. "Nitrosobenzene: Reagent for the Mitsunobu Esterification Reaction." ACS Omega 4, no. 3 (March 7, 2019): 5012–18. http://dx.doi.org/10.1021/acsomega.8b03551.
Full textHarvey, Peta J., and Ian D. Jenkins. "Synthesis of fluorophosphoranes via the mitsunobu reaction." Tetrahedron Letters 35, no. 52 (December 1994): 9775–78. http://dx.doi.org/10.1016/0040-4039(94)88383-1.
Full textHovinen, Jari, and Reijo Sillanpää. "Synthesis of azamacrocycles via a Mitsunobu reaction." Tetrahedron Letters 46, no. 25 (June 2005): 4387–89. http://dx.doi.org/10.1016/j.tetlet.2005.04.078.
Full textSchenk, Stephan, Jennie Weston, and Ernst Anders. "Density Functional Investigation of the Mitsunobu Reaction." Journal of the American Chemical Society 127, no. 36 (September 2005): 12566–76. http://dx.doi.org/10.1021/ja052362i.
Full textSzlenkier, Maurycy, Karol Kamel, and Jerzy Boryski. "Regioselective Mitsunobu Reaction of Partially Protected Uridine." Nucleosides, Nucleotides & Nucleic Acids 35, no. 8 (June 28, 2016): 410–25. http://dx.doi.org/10.1080/15257770.2016.1188943.
Full textShull, Brian K., Takashi Sakai, Jeffrey B. Nichols, and Masato Koreeda. "Mitsunobu Reaction of Unbiased Cyclic Allylic Alcohols." Journal of Organic Chemistry 62, no. 24 (November 1997): 8294–303. http://dx.doi.org/10.1021/jo9615155.
Full textJia, Zhaozhong J., Sandra Kelberlau, Lars Olsson, G. Anilkumar, and Bert Fraser-Reid. "ChemInform Abstract: The Mitsunobu Reaction of Tetrachlorophthalimide." ChemInform 30, no. 38 (June 13, 2010): no. http://dx.doi.org/10.1002/chin.199938133.
Full textGRICE, I. D., P. J. HARVEY, I. D. JENKINS, M. J. GALLAGHER, and M. G. RANASINGHE. "ChemInform Abstract: Phosphitylation via the Mitsunobu Reaction." ChemInform 27, no. 22 (August 5, 2010): no. http://dx.doi.org/10.1002/chin.199622185.
Full textHirose, Daisuke, Martin Gazvoda, Janez Košmrlj, and Tsuyoshi Taniguchi. "Advances and mechanistic insight on the catalytic Mitsunobu reaction using recyclable azo reagents." Chemical Science 7, no. 8 (2016): 5148–59. http://dx.doi.org/10.1039/c6sc00308g.
Full textBeddoe, Rhydian H., Helen F. Sneddon, and Ross M. Denton. "The catalytic Mitsunobu reaction: a critical analysis of the current state-of-the-art." Organic & Biomolecular Chemistry 16, no. 42 (2018): 7774–81. http://dx.doi.org/10.1039/c8ob01929k.
Full textHanaya, Tadashi, Kiyoshi Torigoe, Kazuyuki Soranaka, Horoshi Yamamoto, Yao Qizhengt, and Wolfgang Pfleiderer. "Pteridines CV." Pteridines 6, no. 1 (February 1995): 1–7. http://dx.doi.org/10.1515/pteridines.1995.6.1.1.
Full textB., Unterhalt, and Adam T. "1-(4-Biphenylyl)ethylnitramine, bioisostere Profene." Scientia Pharmaceutica 70, no. 4 (December 5, 2002): 353–58. http://dx.doi.org/10.3797/scipharm.aut-02-34.
Full textSerpico, Luigia, Mauro De Nisco, Flavio Cermola, Michele Manfra, and Silvana Pedatella. "Stereoselective Synthesis of Selenium-Containing Glycoconjugates via the Mitsunobu Reaction." Molecules 26, no. 9 (April 27, 2021): 2541. http://dx.doi.org/10.3390/molecules26092541.
Full textLigi, Maria Cristina, Anna Flis, Giacomo Biagiotti, Giulia Serrano, K. Michał Pietrusiewicz, and Stefano Cicchi. "Heterogeneous Organo- and Metal Catalysis Using Phosphine Oxide Derivatives Anchored on Multiwalled Carbon Nanotubes." C—Journal of Carbon Research 6, no. 3 (September 21, 2020): 57. http://dx.doi.org/10.3390/c6030057.
Full textBurns, Michael J., Thomas O. Ronson, Richard J. K. Taylor, and Ian J. S. Fairlamb. "4-Hydroxy-6-alkyl-2-pyrones as nucleophilic coupling partners in Mitsunobu reactions and oxa-Michael additions." Beilstein Journal of Organic Chemistry 10 (May 20, 2014): 1159–65. http://dx.doi.org/10.3762/bjoc.10.116.
Full textBrulikova, L., Y. Okorochenkova, and J. Hlavac. "A solid-phase synthetic approach to pH-independent rhodamine-type fluorophores." Organic & Biomolecular Chemistry 14, no. 44 (2016): 10437–43. http://dx.doi.org/10.1039/c6ob01772j.
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