Nobel Prize Winning Transition-Metal Mediated Processes
Anant R. Kapdi
Department of Chemistry, Institute of Chemical Technology, Nathalal Parekh Road, Matunga, Mumbai - 400019
DOI: https://doi.org/10.36664/bt/2019/v66i1/148993
Keywords: No Keywords.
Abstract
Transition-metal mediated processes have revolutionized synthetic organic chemistry with the introduction of several Nobel Prize winning reactions which have been highlighted in this review.Downloads
References
J. Clayden, N. Greeves, S. Warren, Organic Chemistry, second edition, Oxford University Press, London, 2012.
A. K. Ghosh, J. Org. Chem. 2010, 75, 7967.
F. Geza, Magyar Kemikusok Lapja, 2014, 69, 38.
H. Bethany, Chem. Eng. News, 2016, 94, 5.
B. Muthuswamy, S. Rangasamy, M. Viswanathan, Mol. Cell. Biochem., 2005, 275, 117.
J. A. Leitch, C. G. Frost, Synthesis, 2018, 50, 2693.
P.Perez, Advances in Organometallic Chemistry, Elsevier, Academic Press, 2018.
V. Grignard, V. Compt. Rend., 1900, 130, 1322.
K. Maruyama, T.Katagiri, J. Phys. Org. Chem., 1989, 2, 205.
W. C. Zeise, Ann. Phys. Chem., 1831, 97, 497.
L. B. Hunt, Platin. Met. Rev., 1984, 28, 76.
W. Ostwald, "Improvements in the Manufacture of Nitric Acid and Nitrogen Oxides", 1902. GB 190200698
M. Bjorkman, S. Widmalm, NOTES REC ROY SOC2010, 64, 379.
F. Bozso, G. Ertl, M. Grunze,M. Weiss, J. Catal., 1977, 49, 18.
E. K. Rideal, Obituary Notices of Fellows of the Royal Society, 1942, 4, 63.
J. G. Dickinson, S. Phillip, ACS Catal., 2014, 4, 2605.
H. J. Taylor, J. Am. Chem. Soc.1944, 66, 4615.
W. G. Jackson, J. A. McKeon, S. Cortez, Inorg. Chem., 2004, 43, 6249.
O. Blacque, B. Heinz, Educacion Quimica,2 015, 26, 330.
M. J. Szollosi, Eur. Rev., 2001, 9, 97.
J. V. Dubrawski, Aust. J. Chem.,2008, 75, 6.
V. A. Filippin, A. V. Krylova, A. N. Zhilova, 1983, VINITI 5531-83, 13.
M. E. Jung, Tetrahedron, 1976, 12, 3.; A. Ichihara, J. Synt. Org. Chem., 1982, 40, 102.
H. B. Kagan, O. Riant, Chem. Rev., 1992, 92. 1007.
L. Pauling, The nature of the chemical bond, Cornell University Press, New York, 1940.
P. Cossee, J. Catal., 1964, 3, 80.
A. G. Potapov, J. Mol Catal., 2017, 432, 155.
A. Vittoria, A. Meppelder, N. Friederichs, V. Busico, R. Cipullo, ACS Catal. 2017, 7, 4509.
H. Sinn, W Kaminsky, Adv. Organomet. Chem., 1980, 18, 99.
A. Bailly; S. Sandis, Ziegler-Natta Catalyst, 1990, United States Patent-4, 960, 741.
J. Dupont, C. S. Consorti, J. Spencer, Chem. Rev. 2005, 105, 2527.
X. Riera, A. Caubet, C. Lopez, V. Moreno, Polyhedron, 1999, 18, 2549.
D. Astruc, Eur. J. Inorg. Chem. 2017, 6.
R. Noyori, Science, 1990, 248, 1195.
R. Noyori, Angew. Chem. Int. Ed., 2002, 41, 2008.
R. Noyori,S. Hashiguchi, Acc. Chem. Res., 1997, 30, 97.
W. S. Knowles, J. Chem. Educ., 1986, 63, 222.
V. Gayakhe, Y. S. Sanghvi, I. J. S. Fairlamb, A. R. Kapdi, Chem. Commun., 2015, 51, 11944.
J. K. Kochi, M. Tamura, J. Am. Chem. Soc., 1971, 93, 1485.
R. F. Heck, J. P. Nolley, J. Org. Chem., 1972, 37, 2320.
K. Sonogashira, Y. Tohda, N. Hagihara, Tetrahedron Lett., 1975, 16, 4467.
B. S. Negishi, J. Am. Chem. Soc., 1976, 98, 6729.
J. K. Stille, Angew. Chem. Int. Ed. Engl., 1986, 25, 508.
N. Miyaura, Y. Kinji, A. Suzuki, Tetrahedron Lett., 1979, 20, 3437.
S. E. Denmark, C. S. Regens, Acc. Chem. Res., 2008, 41, 1486.
A. S.Guram, S. L. Buchwald, L. J. Am. Chem. Soc., 1994, 116, 7901.
C. A. Wheaton, J. J. Bow, M. Stradiotto, Organometallics, 2013, 32, 6148.
S. Bhilare, S. S. M. Bandaru, J. Shah, N. Chrysochos, C. Schulzke, Y. Sanghvi, A. Kapdi, J. Org. Chem., 2018, 83, 13088.
S. Bhilare, V. Gayakhe, A.V. Ardhapure, Y.S. Sanghvi, C. Schulzke, Y. Borozdina, A.R. Kapdi, RSC Adv., 2016, 6, 83820.
H. Ohno, S. Inuki, Synthesis, 2018, 50, 700.
B. Toshikazu, N. Yukiko, S. Kozo, Tetrahedron: Asymmetry, 1997, 8, 2159.
A. S. Sanjeev, S. Ghosh, G. N. Mehta, Archives of Applied Science Research, 2010, 2, 135.
B. Sun, Y. Li, Huaxue Yanjiu Yu Yingyong, 2014, 26, 1645.
M. Paul, A. Murat, M. Wolfgang, P. Werner, Org. Process Res. Dev., 2003, 7, 436.
Y. Sharma, M. Degani, Green Chemistry Letters and Reviews, 2010, 3, 201.