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Advanced Organic Chemistry: Carbonyl Reactivity

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Synthesis Workshop Videos

In this installment of the Synthesis Workshop Advanced Organic Chemistry course, Patrick Deneny joins us to give an overview of carbonyl reactivity.

This episode has an accompanying problem and solution set available at https://synthesisworkshop.com/#probl....

References (in order of appearance):
Fundamentals of Organic Chemistry, 7th ed., Brooks/Cole Cengage Learning, 2011.
Organic Chemistry: A Tenth Edition., OpenStax, 2023. Access for free at openstax.org.
Organic Chemistry, 2nd ed., Oxford University Press, 2012.
Chemistry of the carbonyl group: A stepbystep approach to understanding organic reaction mechanisms, Wiley, 2018
J. Am. Chem. Soc. 1964, 86, 1089
J. Russ. Phys. Chem. Soc. 1911, 43, 582; Lieb. Ann. Chem. 1912, 394, 86; J. Am. Chem. Soc.1964, 86, 2909;
Chem. Ber. 1913, 46, 1837; Org. React. 1975, 22, 401.
J. Chem. Soc. 1946, 39; Tetrahedron Lett. 1968, 9, 3363; Tetrahedron Lett. 1975, 16, 2647; Tetrahedron Lett. 1979, 20, 399; J. Org. Chem. 1983, 48, 4155; J. Am Chem. Soc. 1991, 113, 7277; Tetrahedron 1978, 34, 1651.
Tetrahedron, 1974, 30, 1563; Acc. Chem. Res. 1983, 16, 153; C. R. Acad. Sci. 1900, 130, 1322; Organometallics 2009, 28, 1598.
Tetrahedron Lett., 1968, 9, 2199; J. Am. Chem. Soc. 1973, 95, 6146; Tetrahedron Lett. 1976, 17, 155.
J. Am. Chem. Soc. 1952, 74, 5828; Chem. Rev., 1999, 99, 1191; Tetrahedron Lett. 1994, 35, 8537;
J. Am. Chem. Soc. 1983, 105, 4833; J. Am. Chem. Soc. 1968, 90, 4011; Tetrahedron Lett. 1984, 25, 729
Chemistry of the carbonyl group: A stepbystep approach to understanding organic reaction mechanisms, Wiley, 2018;
J. Am. Chem. Soc. 1964, 86, 2105; J. Am. Chem. Soc. 1981, 103, 5393.
J. Chem. Soc. 1936, 623; Tetrahedron 1976, 32, 2979.
; J. Org. Chem. 1963, 28, 3362; Tetrahedron 1976, 32, 2979; J. Am. Chem. Soc. 1961, 83, 13, 2965.
J. Am. Chem. Soc. 1981, 103, 2127; J. Am. Chem. Soc. 1982, 104, 1737; Tetrahedron, 2014, 70, 2207; RSC Adv. 2016, 6, 30498; Tetrahedron Lett. 1981, 22, 3815; Synthesis, 2008, 2008, 3707.
J. Am. Chem. Soc. 2011, 133, 11936; J. Am. Chem. Soc. 2013, 135, 16853.
Bull Chim. Soc. Fr. 1872, 436; J. Am. Chem. Soc. 1973, 95, 3310; J. Org. Chem. 2016, 81, 5631; Synthesis, 1991, 2, 795.
J. Am. Chem. Soc. 1957, 79, 1920; Tetrahedron Lett. 1975, 16, 1225; J. Am. Chem. Soc. 1979, 101, 6120; J. Org. Chem. 1980, 45, 1066; J. Am. Chem. Soc. 1989, 111, 3441.
J. Am. Chem. Soc. 1979, 101, 6120; J. Am. Chem. Soc. 1981, 103, 2127; J. Am. Chem. Soc. 1981, 103, 3099;
Angew. Chem. Int. Ed. 2014, 53, 2692; Chem. Commun. 2021, 57, 3171.
J. Am. Chem. Soc. 1954, 76, 2029; J. Am. Chem. Soc. 1963, 85, 207; J. Am. Chem. Soc. 1970, 92, 4261.
J. Am. Chem. Soc. 2000, 122, 2395; J. Am. Chem. Soc. 2001, 123, 12911; Chem. Rev. 2007, 107, 5471; Angew. Chem. Int. Ed. 2005, 44, 794; Angew. Chem. Int. Ed. 2005, 44, 4212; J. Am. Chem. Soc. 2005, 127, 18296; Synlett 2012, 23, 953.
Angew. Chem. Int. Ed. 1979, 18, 239.
Angew. Chem. Int. Ed. 1965, 4, 1007; J. Org. Chem. 1966, 31, 4097; J. Org. Chem. 1975, 40, 231; Synthesis, 1977, 1977, 357; Acc. Chem. Res. 2004, 37, 365.
Ann. Pharm. 1832, 3, 249; Ann. Pharm. 1839, 31, 329; J. Chem. Soc. 1903, 83, 995.
J. Pharm. Soc. Jpn. 1943, 63, 296; J. Am. Chem. Soc. 1958, 80, 3719; Chem. Lett. 2008, 37, 534; J. Org. Chem. 2009, 74, 23, 9214; Beilstein J. Org. Chem. 2016, 12, 444.

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