Abstract
Alkanes, being saturated hydrocarbons cannot be reduced any further. However,
cycloalkanes give alkanes on catalytic hydrogenation in quantitative yield.
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References
R. Willstätter and J. Bruck, Chem. Ber., 1907, 40, 3979, 4456.
N.D. Zelinsky, B.A. Kazanka and A.F. Plate, Chem. Ber., 1933, 66, 1415
A.P.G. Kieboom, H.J. Van Benschop and H. Van Bekkum, Rec. Tranv. Chim. Pays-Bas, 1976, 95, 231.
S. Siegel and G.V. Smith, J. Am. Chem. Soc., 1960, 82, 6082.
J.H.P. Tyman and S.W. Wolkins, Tetrahedron Lett., 1973, 1773.
D.N. Kursanov, Z.N. Parnes and N.M. Loim, Synthesis, 1974, 633.
D.N. Kursanov, Z.N. Parnes G.I. Bassova, N.M. Loim and V.I. Zdanovich, Tetrahedron, 1967, 23, 2235.
E.E. Van Tamelen and R.J. Timmons J. Am. Chem. Soc., 1962, 84, 1067.
H.C. Brown and C.A. Brown, J. Am. Chem. Soc., 1963, 85, 1005.
C.A. Brown and V.K. Ahuja, Chem. Commun., 1973, 553.
C.A. Brown, J. Org. Chem., 1970, 35, 1900.
W.F. Newhall, J. Org. Chem., 1958, 23, 1247.
T. Moidgley and A.L. Henne, J. Am. Chem. Soc., 1929, 51, 1293.
K. Ziegler, F. Häffner and H. Grimm., Ann. Chem., 1937, 528, 101.
K. Zigler and H. Wilms, Ann. Chem., 1950, 567, 1, 36.
K. Zigler, L. Jakob, H. Wollthan and A. Wenz, Ann. Chem., 1934, 511.
P.B. Lumb and J.C. Smith, J. Chem. Soc., 1952, 5032.
D.R. Howton and R.H. Davis, J. Org. Chem., 1951, 16, 1405.
S. Bance, H.J. Barber and A.M. Woolmann, J. Chem. Soc., 1943, 1.
K.N. Campbell and M.A. O’Connor, J. Am. Chem. Soc., 1939, 61, 2896.
K.N. Campbell and L.T. Eby, J. Am. Chem. Soc., 1941, 63, 216.
E.F. Magon and L.H. Slaugh, Tetrahedron, 1967, 23, 4509.
G. Zweifel and R.B. Steele, J. Am. Chem. Soc., 1967, 89, 5085.
G. Wilke and H. Müller, Chem. Ber., 1956, 89, 444.
A. Skita and A. Schneck, Chem. Ber., 1922, 55, 144.
R. Adams and R.L. Shriner, J. Am. Chem. Soc., 1923, 45, 2171.
R. Adams, V. Voorhees and R.L. Shriner, Org. Synth Coll Vol., 1932, 1, 463.
J.J. Brunet, P. Gallois and P. Caubere, J. Org. Chem., 1980, 45, 1957, 1946.
E.C. Ashby, J.J. Lin and A.B. Goel, J. Org. Chem., 1978, 43, 757.
J.R. Weiz, B.A. Patel and R.F. Heck, J. Org. Chem. 1980, 45, 4926.
N.A. Dobson and R.A. Raphael, J. Chem. Soc., 1955, 3558.
J. Sicher, M. Svoboda and J. Zdvada, Collect. Czech. Chem. Commun, 1965, 30, 421.
M. Svoboda, J. Závada and J. Sicher, Collect. Czech. Chem. Commun., 1965, 30, 413.
A.T. Blomquist, L.H. Liu and J.C. Bohrer, J. Am. Chem. Soc., 1952, 74, 3643.
R.H. Baker and R.D. Schutz, J. Am. Chem. Soc., 1947, 69, 1250.
H. Adkins and W.A. Reed, J. Am. Chem. Soc., 1941, 63, 741.
R. Willstätter and F. Seitz., Chem. Ber., 1923, 56, 1388.
E.S. Cook and A.J. Hill, J. Am. Chem. Soc., 1940, 62, 1995.
W. Hückel and H. Bretschnider, Ann. Chem., 1939, 540, 157.
A.J. Birch, A.R. Murray and H. Smith, J. Chem. Soc., 1951, 1945.
W. Hückel and H. Schlee, Chem. Ber., 1955, 88, 346.
R.A. Benkeser and E.M. Kaiser, J. Org. Chem., 1964, 29, 955.
L. Reggel, R.A. Friedel and I. Wender, J. Org. Chem., 1957, 22, 89.
W. Hückel and U. Wo¨ rffel, Chem. Ber., 1956, 89, 2098.
M. Orchin, J. Am. Chem. Soc., 1944, 66, 535.
L.S. Stuhl, M. DuBois Rakowski, F.J. Hirsekorn, J.R. Bleeke, A.E. Stevens and E.L. Muetterties, J. Am. Chem. Soc., 1978, 100, 2405.
K.C. Bass, Org. Syn. Coll. Vol., 1973, 5, 398.
N.S. Crossley and H.B. Henbest, J. Chem. Soc., 1960, 4413.
J.R. Durland and H. Adkins, J. Am. Chem. Soc., 1937, 59, 135; 1938, 60, 1501.
A. Burger and E. Mosettig, J. Am. Chem. Soc., 1935, 57, 2731; 1936, 58, 1857.
D.D. Phillips, Org. Syn. Coll. Vol., 1963, 4, 313.
E. Bamberger and W. Lodter, Chem. Ber., 1887, 20, 3073.
D. Starr and R.M. Hixon, Org. Syn. Coll. Vol., 1943, 2, 566.
R. cannor and H. Adkins, J. Am. Chem. Soc., 1932, 54, 4678.
D.S. Torbell and C. Weaver, J. Am. Chem. Soc., 1941, 63, 2939.
J. Entel, C.H. Ruof and H.C. Howard, J. Am. Chem. Soc., 1951, 73, 4152.
E. Campaigne and J.L. Diedrich, J. Am. Chem. Soc., 1951, 73, 5240.
H. Greenfield, S. Metlin, M. Orchin and I. Wender, J. Org. Chem., 1958, 23, 1054.
R. Adams and B.S. Garvey, J. Am. Chem. Soc., 1926, 48, 477.
L.C. Craig and R.M. Hixon, J. Am. Chem. Soc., 1930, 52, 804; 1931, 53, 188.
F.K. Singaigo and H. Adkins, J. Am. Chem. Soc., 1936, 58, 709.
C.G. Overberger, L.C. Palmer, B.S. Marks and N.R. Byrd, J. Am. Chem. Soc., 1955, 77, 4100.
G.W. Gribble, P.D. Lord, J. Skotnicki, S.E. Dietz, J.T. Eaton and J.L. Johnson, J. Am. Chem. Soc., 1974, 96, 7812.
J.G. Berger, Synthesis, 1974, 508.
Y. Kikugawa, K. Saito and S. Yamada, Synthesis, 1978, 447.
L.J. Dolby and G.W. Gribble, Heterocyc. Chem., 1966, 3, 124.
H. Adkins and H.L. Coontradt, J. Am. Chem. Soc., 1941, 63, 1563.
D.V. Young and H.R. Snyder, J. Am. Chem. Soc., 1961, 83, 3160.
F.E. King, J.A. Barltrop and R.J. Walley, J. Chem. Soc., 1945, 277.
S. O’Brien and D.C.C., Smith, J. Chem. Soc., 1960, 4609.
H. Adkins, L.F. Kuick, M. Farlow and B. Wojeik, J. Am. Chem. Soc.,1934, 56, 2425.
M. Freifelder and G.R. Stone J Org. Chem., 1961, 26, 3805.
M. Freifelder, Advan. Catalysis, 1963, 14, 203.
W. Hückel and L. Hagedorn, Chem. Ber., 1957, 90, 752.
H. Adkins and H.I. Cramer, J. Am. Chem. Soc., 1930, 52, 4349.
W. Hückel and F. Stepf, Ann. Chem., 1927, 453, 163.
S. Landa and J. Mostecky’, Collect. Czech. Chem. Commun., 1955, 20, 430.
J.J. Brewster, S.F. Osman, H.O. Bayer and H.B. Hopps, J. Org. Chem., 1964, 29, 121.
E. Vowinkel and I. Buthe, Chem. Ber., 1974, 107, 1353.
L. Barth and G. Goldschmiedt. Chem. Ber., 1879, 12, 1244.
T. Severin and I. Ipach, Synthesis, 1973, 796.
E. Vowinkel and C. Wolf, Chem. Ber., 1974, 107, 907.
G.W. Gribble, R.M. Leese and B. Evans, Synthesis, 1977, 172.
J.H. Brewster and H.O. Bayer, J. Org. Chem., 1964, 29, 105, 110.
C.S. Marvel, F.D. Hager and E.C. Caudle, Org. Synth. Coll. Vol., 1932, 1, 224.
S. Nishimura, T. Onoda and A. Nakamura, Bull. Chem. Soc. Japan,
1960, 33, 1356; F.A. Hochstein and W. G. Brown, J. Am. Chem. Soc.,
, 3484.
R.H. Baker and R.D. Schuetz, J. Am. Chem. Soc., 1947, 69, 1250.
H. Adkins and H.I. Cramer, J. Am. Chem. Soc., 1930, 52, 4349.
V.K. Ahluwalia, Chandra Prakash and R.P. Singh, Ind. J. Chem., 1978, 16 B, 587; V.K. Ahluwalia and S. Mehta, Ind. J. Chem., 1978, 16 B, 977.
M.K. autmann and P. Pannevitz. Ber., 1912, 90, 6636.
R.F. Nystron and W.G. Broun, J. Am. Chem. Soc., 1947, 69, 1197.
R.F. Nystrom, S.W. Claikin and W.G. Broun, J. Am. Chem. Soc., 1949, 71, 3245.
S.W. Chaikin and W.G. Brown. J. Am. Chem. Soc., 1949, 71, 122.
S. Krishnamurty, J. Org. Chem., 1981, 46, 4628.
V. Ba•ant, M. Čapka, M. Černý, V. Chvalovský, K. Kochloeff, M. Kvaus and M. Mdlek, Tetrahedran Lett., 1968, 3303.
D.J. Brown and P. Waring, Austral, J. Chem., 1973, 26, 443.
G. Bouveault and G. Blanc, Compt. Rend., 1903, 136, 1676, Bull. Soc. Chem. France, 1904, (3) 31, 666.
V. Grigrard, Compt. Rend., 1900, 130, 1322, V.K. Ahluwalia and R.K. Parashar, Organic Reaction Mechanism, Narosa Publishing House, 2007, page 475.
E.L. Martin, Org. Reactions, 1942, 1, 155.
E. Clemmensen, Chem. Ber., 1913, 46, 1837.
D. Todd, Org. Reactions, 1948, 4, 378.
C.H. Herr, F.C. Whitmore and R.W. Schiessler, J. Am. Chem. Soc., 1945, 67, 2061.
R. Adams and B.S. Carvey, J. Am. Chem. Soc., 1926, 48, 477.
P.N. Rylander and D.R. Steele, Tetrahedron Lett., 1969, 1579.
W.G. Young, W.H. Hartung and F.S. Crossley, J. Am. Chem. Soc., 1936, 58, 100; H. Meerwein, Liebigs Ann., 1925, 444, 221; W. Ponndorf, Angew. Chem., 1926, 39, 138; A. Verly, Bull. Soc. Chem. Fr., 1925, 37, 537.
R.C. Brannock, J. Am. Chem. Soc., 1959, 81, 3379.
R. Mozingo, Org. Synth., Coll. Vol., 1955, 3, 685.
H.D. Law, J. Chem. Soc., 1912, 101, 1016.
T.W. Russell, D.M. Duncan and S.C. Hansen, J. Org. Chem., 1977, 42, 551.
K. Nanjo, K. Suzuki and M. Sekiya, Chem. Lett., 1976, 1169.
A. Sketa, Chem. Ber., 1915, 48, 1486.
J.J. Brunet, P. Gallois and P. Canbere, J. Org. Chem., 1980, 45, 1937.
T. Fujisawa, K. Sugimoto and H. Ohla, J. Org. Chem., 1976, 41, 1667.
H.C. Brown and E.J. Mead, J. Am. Chem. Soc., 1953, 75, 6263.
D.J. Raber and W.C. Guido, J. Org. Chem., 1976, 41, 690.
B.R. Brown and A.M.S. White, J. Chem. Soc., 1957, 3755.
D. Davidson and M. Welss, Org. Syn. Coll. Vol., 1943, 2, 590.
M.M. Midland, S. Greer, A. Trammtano and S.A. Zderic, J. Am. Chem. Soc., 1979, 101, 2352.
T.P.C. Mulholland and G. Ward, J. Chem. Soc., 1954, 4676.
J.L. Fry, M. Orfanopoulos, M.G. Adlington, W.P. Dittman, Jr., and S. B. Silverman, J. Org. Chem., 1978, 43, 372.
R. Schovarz and H. Hering, Org. Syn. Coll. Vol., 1963, 4, 203.
G. Lock and K. Stack, Chem. Ber., 1943, 76, 1252.
L. Caglioti, Tetrahedron, 1966, 22, 487.
T.W. Russell, D.M. Duncan and S.C. Hansen, J. Org. Chem., 1977, 42, 551.
H. Adkin and H.R. Billica, J. Am. Chem. Soc., 1948, 70, 695; Org. Syn Coll. Vol., 1955, 3, 176.
M.J. Jorgenson, Tetrahedron Lett., 1962, 559.
R.O. Hutchins and D.K. Andasamy, J. Org. Chem., 1975, 40, 2530.
R.O. Hutchins, B.E. Margnoff and C.A. Milewski, J. Am. Chem. Soc., 1971, 93, 1793.
S. Nishimura, Bull. Chem. Soc. Japan, 1961, 34, 32.
H. Adkins and R. Connor, J. Am. Chem. Soc., 1931, 53, 1091.
J. Plešek, S. Mer^mánek, Collect. Czech. Chem. Common., 1966, 31, 3060.
K. Heusler, P. Wieland and C.H. Meysfre, Org. Syn Coll. Vol., 1973, 5, 692.
E.L. Eliel and D. Nasipuri, J. Org. Chem., 1965, 30, 3809.
H.C. Brown, S.C. Kin and S. Krishnamurthy, J. Org. Chem., 1980, 45, 1.
E. Santaniello, F. Ponti and A. Manzocchi, Synthesis, 1978, 891.
R.O. Hutchins and N.R. Natale, J. Org. Chem., 1978, 43, 2299.
G.W. Kabalka and S.T. Summers, J. Org. Chem., 1981, 46, 1217.
G.R. Pettit and E.E. Van Tamelen, Org. Reactions, 1962, 12, 356.
M.L. Wolfrom and J.V. Karabinos, J. Am. Chem. Soc., 1944, 66, 909.
A. Adams and E.W. Adams, Org. Syn. Coll. Vol. 1932, 1, 459.
P.L. Cook, J. Org. Chem., 1962, 21, 3873.
J.H.P. Tyman, J. Appl. Chem., 1970, 20, 179.
D.J. Gram and F.A. Abd Elhafer, J. Am. Chem. Soc., 1952, 74, 5828.
R.O. Hutchins and D. Kandasamy, J. Am. Chem. Soc., 1973, 95, 613.
J.G. de Vries and R.M. Kellogg, J. Org. Chem., 1980, 45, 4126.
D. Seebach and H. Down, Chem. Ber., 1974, 107, 1748.
T.J. Donohoe, Oxidations and Reductions in Organic Syntheis, Oxford Science Publications 2000, page 68.
S. Yamashita, J. Organometal. Chem., 1968, 11, 377.
K. Kabuto, M. Imuta, E.S. Kempner and H. Ziffer, J. Org. Chem., 1978, 43, 2357.
(a). J. S Yadav, S. Nanda, P.T. Reddy and A.B. Rau, J. Org. Chem., 2000, 67, 3900.
M. Imuta and H. Ziffer, J. Org. Chem., 1978, 43, 3530.
E. Kienan, E.K. Hafeli, K.K. Seth and R. Lamed, J. Am. Chem. Soc., 1986, 108, 162.
P.A. Plattner, A. Fürst and W. Keller, Helv. Chem. Acta, 1949, 32, 2464.
F.K. Sigaigo and H. Adkins, J. Am. Chem. Soc., 1936, 58, 709.
G.W. Gribble, W.J. Kelly and S.E. Emery, Synthesis, 1978, 763.
A. Klages and P. Allendorff, Chem. Ber., 1898, 31, 998.
R.R. Read and J. Wood, Jr., Org. Syn. Coll. Vol. 1955, 3, 444.
W.B. Wahalley, J. Chem. Soc., 1951, 665.
L. Caglioti and M. Magi, Tetrahedron, 1963, 19, 1127.
R. Helg, H. Schinz and E.L. Eliel, Helv. Chem. Acta, 1952, 35, 2406.
E.L. Eliel and R.S. Ro, J. Am. Chem. Soc., 1957, 79, 5992.
D.H.R. Barton and C.H. Robinson J. Chem. Soc., 1954, 3045.
H.O. House, Modern Synthetic Reductions, 2nd Edn., 1972, page 175 (Menlo Park, California, Benjamin).
D.H.R. Bartan, Helv Chem. Acta, 1953, 1027, Note 23.
G.W. Kabalka, D.T.C. Yang and J.D. Baker, J. Org. Chem., 1976, 41, 574.
K. Biemann, G. Büchi and B.H. Walker, J. Am. Chem. Soc., 1957, 79, 5558.
E.F. Rosenblatt, J. Am. Chem. Soc., 1940, 62, 1092.
R.F. Nystrom and W.G. Brown, J. Am. Chem. Soc., 1948, 70, 3738.
A.J. Fatiadi and W.F. Sager, Org. Syn. Coll. Vol., 1973, 5, 595.
F. Russig, J. Prakt. Chem., 1900, 62, 30.
J. Schmidt and A. Kampf, Chem., Ber., 1902, 35, 3124.
M.L. Moore, Org. Reactions, 1949, 5, 301.
W.S. Emersan, Org. Reactions, 1948, 4, 174.
M. Muraki and T. Mukaiyama, Chem. Lett., 1974, 1447.
J. Tafel and G. Friedrichs, Chem. Ber., 1904, 37, 3187.
R.L. Augustine, J. Org. Chem., 1958, 23, 1853.
M. Černý, J. Málek, M. Čapka and V. Chvalovský, Collect. Czech. Chem. Common., 1969, 34, 1025.
M. Černý and J. Málek, Collect. Czech. Chem. Common., 1971, 36, 2394.
N.M. Yoon, C.S. Pak, H.C. Brown, S. Krishnamurty and T.P. Stocky, J. Org. Chem., 1973, 38, 2786.
G.E. Benedict and R.R. Russel, J. Am. Chem. Soc., 1951, 73, 5444.
T.M. Donohoe, Oxidations and Reduction in Organic Synthesis, Oxford Science Publication 2000, page 72.
K.W. Rosenmund, Ber., 1921, 54, 438.
E. Mosettig and R. Mozingo, Org. Reactions 1948, 4, 362.
J.D. Citron, J. Org. Chem., 1969, 34, 1977.
H.C. Brown and R.F. McFarlin, J. Am. Chem. Soc., 1958, 80, 5372.
H.C. Brown and B.C. Subba Ravo, J. Am. Chem. Soc., 1958, 80, 5377.
T.N. Sorrell and P.S. Pearlman, J. Org. Chem., 1980, 45, 3449.
L. Horner and H. Röder, Chem. Ber., 1970, 103, 2984.
J. Plešek and S. Hérmánek, Collect. Chech. Chem. Common., 1966, 31, 3060.
P.R. Austin, E.W. Bousquet and W.A. Lazeir, J. Am. Chem. Soc., 1937, 59, 864.
V. Ba•ant, M. Čapra, M. Černý, V. Chvalovský, K. Kochloeff, M. Kraus and J. Málek, Tetrahedron Lett., 1968, 3303.
L.I. Zakharin, V.V. Gavrikenko, D.N. Maslin, and I.M. Khorlina, Tetrahedron Lett., 1963, 2087.
L.I. Zakharin and I.M. Khorlina, Tetrahedron Lett., 1962, 619.
M. Maraki and T. Murkaiyama, Chem. Lett., 1975, 215.
G. Bouveault and G. Blanc. Compt. Rend., 1903, 136, 1676; Bull. Soc. Chem. France, 1904, 31, 666; H.O. House, Modern Synthetic Reactions, W.A. Benjamen, California, 1972, p. 150.
H. Adkins and R.H. Gillespie, Org. Syn. Coll. Vol., 1953, 3, 361.
L. Bouveault and R. Loguin, Compt. Rend., 1905, 140, 1593.
V.L. Hansley, J. Am. Chem. Soc., 1935, 57, 2303.
V. Prelog, L. Frenkiel, M. Kobelt and P. Barman, Helv. Chem. Acta, 1947, 30, 174.
T.J. Donohoe, Oxidation and Reduction in Organic Synthesis, Oxford Science, Publication 2000, page 71 and 74.
H.C. Brown and A. Tsukamoto, J. Am. Chem. Soc., 1964, 86, 1089.
V.M. Micovic’ and M.L. Mihailovic’, J. Org. Chem., 1953, 18, 1190.
M.M. Walborsky, M. Baum and D.F. Lonirine J. Am. Chem. Soc., 1955, 77, 3637.
H.C. Brown and S.C. Kim, Synthesis, 1977, 635.
B.D. James, Chem. Ind., 1971, 227.
N.M. Yoon and H.C. Brown, J. Am. Chem. Soc., 1968, 90, 2927.
N. Umino, T. Ikawuma and N. Itoh, Tetrahedron Lett., 1976, 763.
H.C. Brown and P. Heim, J. Am. Chem. Soc., 1964, 86, 3566; J. Org. Chem. 1973, 38, 912.
M.E. Kuehne and B.F. Lamberl, J. Am. Chem. Soc., 1959, 81, 4278, Org. Syn Coll. Vol., 1973, 5, 400.
E.S. Wallis and J.F. Lane, OR, 1946, II, 267; A. W. Hotmann, Ber., 1881, 14, 2725.
H. Schindlbaur, Montash, 1969, 100, 1413.
J. Tafel and M. Stern, Chem. Ber., 1900, 33, 2224.
Y. Kindo and B. Witkop, J. Org. Chem., 1968, 33, 206.
A. Dunet, R. Roller and A. Willemart, Bull. Soc. Chem., Fr., 1950, 877.
A. Calder and S.P. Hepburn, Org. Syn., 1972, 52, 77.
M. Senkus, Ind. Eng. Chem., 1948, 40, 506.
A.T. Nielsen, J. Org. Chem., 1962, 27, 1998.
V. Broun and W. Sobecki, Chem. Ber., 1911, 44, 2526, 2533.
A.A. Artemev, A.B. Genkina, A.B. Malimonova, V.P. Trofilkina and M.A. Isalnkova, Zh. Ves. Khun. Obschestva im. D.I. Mendeleeva, 1965, 10, 588, Chem. Abstr. 1966, 64, 1975.
H.E. Bigelow and A. Palner, Org. Syn. Coll. Vol., 1943, 2, 5.
K. Brand and J. Steiner Chem. Ber., 1922, 55, 875, 886.
B.D. James, Chem. Ind., 1971, 227.
H.E. Bigelow and D.B. Robinson, Org. Syn. Coll. Vol., 1955, 3, 103.
H. Wislicenus, Chem Ber., 1896, 29, 494.
O. Kamn, Org. Syn. Coll. Vol., 1932, 1, 445.
R.W. West, J. Chem. Soc., 1925, 127, 494.
T.F. Dankova, T.N. Bokova and N.A. Preobrazhenskii, Zh. Obschei Khim., 1951, 21, 787, Chem. Abstr., 1951, 45, 9517.
H.H. Hodgson and E.R. Wand, J. Chem. Soc., 1947, 327.
M.O. Terpko and R.F. Heck. J. Org. Chem., 1980, 45, 4992.
H. Stephen, J. Am. Chem. Soc., 1925, 127, 1874.
E. Mosettig, Organic Reactions, 1954, 8, 232.
T.S. Gardner, F.A. Smith, E. Wenis and J. Lee, J. Org. Chem., 1951, 16, 1121.
R.C. Fuson, W.D. Emmons and R. Tull, J. Org. Chem., 1951, 16, 648.
G. Hesse and R. Schroedel, Ann. Chem., 1957, 607, 24.
H.C. Brown and C.P. Garg, J. Am. Chem. Soc., 1964, 86, 1085.
M. Freifelder, J. Am. Chem. Soc., 1960, 82, 2386.
A. Albert and D. Magrath, J. Chem. Soc., 1944, 678.
L.H. Amundsen and L.S. Nelson, J. Am. Chem. Soc., 1951, 73, 242.
H.C. Brown and P.M. Weissmann, J. Am. Chem. Soc., 1965, 87, 5614.
H.C. Brown and B.C. Subba Rao, J. Am. Chem. Soc., 1956, 78, 2582.
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Ahluwalia, V.K. (2023). Reduction of Specific Types of Organic Compounds. In: Reduction in Organic Synthesis. Springer, Cham. https://doi.org/10.1007/978-3-031-37686-3_3
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