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Reviews of glyoxylates in organic synthesis: (a) Mikami, K. Pure Appl. Chem. 1996, 68, 639; (b) Johannsen, M.; Yao, S.; Graven, A.; Jørgensen, K. A. Pure Appl. Chem. 1998, 70, 1117; (c) Jurczak, J.; Bauer, T. Pure Appl. Chem. 2000, 72, 1589.
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Mikami, K.1
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Reviews of glyoxylates in organic synthesis: (a) Mikami, K. Pure Appl. Chem. 1996, 68, 639; (b) Johannsen, M.; Yao, S.; Graven, A.; Jørgensen, K. A. Pure Appl. Chem. 1998, 70, 1117; (c) Jurczak, J.; Bauer, T. Pure Appl. Chem. 2000, 72, 1589.
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Johannsen, M.1
Yao, S.2
Graven, A.3
Jørgensen, K.A.4
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Reviews of glyoxylates in organic synthesis: (a) Mikami, K. Pure Appl. Chem. 1996, 68, 639; (b) Johannsen, M.; Yao, S.; Graven, A.; Jørgensen, K. A. Pure Appl. Chem. 1998, 70, 1117; (c) Jurczak, J.; Bauer, T. Pure Appl. Chem. 2000, 72, 1589.
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Pure Appl. Chem.
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Jurczak, J.1
Bauer, T.2
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Review of α-hydroxy carboxylic acids:
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Review of α-hydroxy carboxylic acids: Gröger H. Adv. Synth. Catal. 343:2001;547.
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Adv. Synth. Catal.
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Gröger, H.1
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Reviews of bowl-shaped compounds: (a) Goto, K.; Okazaki, R. Liebigs Ann./Recueil 1997, 2393; (b) Saito, S.; Yamamoto, H. Chem. Commun. 1997, 1585.
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Liebigs Ann./Recueil
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Goto, K.1
Okazaki, R.2
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10
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0002238366
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Reviews of bowl-shaped compounds: (a) Goto, K.; Okazaki, R. Liebigs Ann./Recueil 1997, 2393; (b) Saito, S.; Yamamoto, H. Chem. Commun. 1997, 1585.
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(1997)
Chem. Commun.
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Saito, S.1
Yamamoto, H.2
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11
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0034684212
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Chemistry of bowl-shaped tris(2,6-diphenylbenzyl)silyl group: (a) Iwasaki, A.; Kondo, Y.; Maruoka, K. J. Am. Chem. Soc. 2000, 122, 10238; (b) Shirakawa, S.; Komatsu, N.; Iwasaki, A.; Maruoka, K. Synlett 2002, 577; (c) Shirakawa, S.; Maruoka, K. Tetrahedron Lett. 2002, 43, 1469.
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Iwasaki, A.1
Kondo, Y.2
Maruoka, K.3
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12
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0036214930
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Chemistry of bowl-shaped tris(2,6-diphenylbenzyl)silyl group: (a) Iwasaki, A.; Kondo, Y.; Maruoka, K. J. Am. Chem. Soc. 2000, 122, 10238; (b) Shirakawa, S.; Komatsu, N.; Iwasaki, A.; Maruoka, K. Synlett 2002, 577; (c) Shirakawa, S.; Maruoka, K. Tetrahedron Lett. 2002, 43, 1469.
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Synlett
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Shirakawa, S.1
Komatsu, N.2
Iwasaki, A.3
Maruoka, K.4
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13
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0037127572
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Chemistry of bowl-shaped tris(2,6-diphenylbenzyl)silyl group: (a) Iwasaki, A.; Kondo, Y.; Maruoka, K. J. Am. Chem. Soc. 2000, 122, 10238; (b) Shirakawa, S.; Komatsu, N.; Iwasaki, A.; Maruoka, K. Synlett 2002, 577; (c) Shirakawa, S.; Maruoka, K. Tetrahedron Lett. 2002, 43, 1469.
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Tetrahedron Lett.
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Shirakawa, S.1
Maruoka, K.2
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14
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0035910486
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For related study on the similar bowl-shaped tris(2,6-diphenylbenzyl)tin hydride and tris(2,6-diphenylbenzyl)amine, see: (a) Sasaki, K.; Kondo, Y.; Maruoka, K. Angew. Chem., Int. Ed. 2001, 40, 411; (b) Sasaki, K.; Komatsu, N.; Shirakawa, S.; Maruoka, K. Synlett 2002, 575; (c) Naiki, M.; Shirakawa, S.; Kon-i, K.; Kondo, Y.; Maruoka, K. Tetrahedron Lett. 2001, 42, 5467.
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Angew. Chem., Int. Ed.
, vol.40
, pp. 411
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Sasaki, K.1
Kondo, Y.2
Maruoka, K.3
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15
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0036219221
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For related study on the similar bowl-shaped tris(2,6-diphenylbenzyl)tin hydride and tris(2,6-diphenylbenzyl)amine, see: (a) Sasaki, K.; Kondo, Y.; Maruoka, K. Angew. Chem., Int. Ed. 2001, 40, 411; (b) Sasaki, K.; Komatsu, N.; Shirakawa, S.; Maruoka, K. Synlett 2002, 575; (c) Naiki, M.; Shirakawa, S.; Kon-i, K.; Kondo, Y.; Maruoka, K. Tetrahedron Lett. 2001, 42, 5467.
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(2002)
Synlett
, pp. 575
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Sasaki, K.1
Komatsu, N.2
Shirakawa, S.3
Maruoka, K.4
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16
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0035817261
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For related study on the similar bowl-shaped tris(2,6-diphenylbenzyl)tin hydride and tris(2,6-diphenylbenzyl)amine, see: (a) Sasaki, K.; Kondo, Y.; Maruoka, K. Angew. Chem., Int. Ed. 2001, 40, 411; (b) Sasaki, K.; Komatsu, N.; Shirakawa, S.; Maruoka, K. Synlett 2002, 575; (c) Naiki, M.; Shirakawa, S.; Kon-i, K.; Kondo, Y.; Maruoka, K. Tetrahedron Lett. 2001, 42, 5467.
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Tetrahedron Lett.
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Naiki, M.1
Shirakawa, S.2
Kon-I, K.3
Kondo, Y.4
Maruoka, K.5
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17
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0035528531
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Another example of bowl-shaped silyl compounds with shallow cavity:
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Another example of bowl-shaped silyl compounds with shallow cavity: Goto K., Okumura T., Kawashima T. Chem. Lett. 2001;1258.
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Chem. Lett.
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Goto, K.1
Okumura, T.2
Kawashima, T.3
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0012004271
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Attempted synthesis of triisopropylsilyl glyoxylate by ozonolysis of triisopropylsilyl acrylate resulted in formation of polymeric products.
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Attempted synthesis of triisopropylsilyl glyoxylate by ozonolysis of triisopropylsilyl acrylate resulted in formation of polymeric products.
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19
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0032491845
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Evans D.A., Trotter B.W., Côté B., Coleman P.J., Dias L.C., Tyler A.N. Angew. Chem., Int. Ed. Engl. 36:1997;2744.
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Diastereoselective aldol reactions of glyoxylates: (a) Mikami, K.; Matsukawa, S. J. Am. Chem. Soc. 1993, 115, 7039; (b) Evans, D. A.; MacMillan, D. W. C.; Campos, K. R. J. Am. Chem. Soc. 1997, 119, 10859.
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Diastereoselective aldol reactions of glyoxylates: (a) Mikami, K.; Matsukawa, S. J. Am. Chem. Soc. 1993, 115, 7039; (b) Evans, D. A.; MacMillan, D. W. C.; Campos, K. R. J. Am. Chem. Soc. 1997, 119, 10859.
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Campos, K.R.3
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Carreira, E.M.1
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0000032580
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Yamamoto, H., Ed.; Wiley-VCH: Weinheim
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4 is increased due to its octahedral coordination. See: (a) Urabe, H.; Sato F. In Lewis Acids in Organic Synthesis; Yamamoto, H., Ed.; Wiley-VCH: Weinheim, 2000; Vol. 2; p. 653; (b) Shambayati, S.; Crowe, W. E.; Schreiber, S. L. Angew. Chem., Int. Ed. Engl. 1990, 29, 256; (c) Walker, M. A.; Heathcock, C. H. J. Org. Chem. 1991, 56, 5747; (d) Cozzi, P. G.; Solari, E.; Floriani, C.; Chiesi-Villa, A.; Pizzol, C. Chem. Ber. 1996, 129, 1361.
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Urabe, H.1
Sato, F.2
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4 is increased due to its octahedral coordination. See: (a) Urabe, H.; Sato F. In Lewis Acids in Organic Synthesis; Yamamoto, H., Ed.; Wiley-VCH: Weinheim, 2000; Vol. 2; p. 653; (b) Shambayati, S.; Crowe, W. E.; Schreiber, S. L. Angew. Chem., Int. Ed. Engl. 1990, 29, 256; (c) Walker, M. A.; Heathcock, C. H. J. Org. Chem. 1991, 56, 5747; (d) Cozzi, P. G.; Solari, E.; Floriani, C.; Chiesi-Villa, A.; Pizzol, C. Chem. Ber. 1996, 129, 1361.
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Shambayati, S.1
Crowe, W.E.2
Schreiber, S.L.3
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27
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0342713705
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4 is increased due to its octahedral coordination. See: (a) Urabe, H.; Sato F. In Lewis Acids in Organic Synthesis; Yamamoto, H., Ed.; Wiley-VCH: Weinheim, 2000; Vol. 2; p. 653; (b) Shambayati, S.; Crowe, W. E.; Schreiber, S. L. Angew. Chem., Int. Ed. Engl. 1990, 29, 256; (c) Walker, M. A.; Heathcock, C. H. J. Org. Chem. 1991, 56, 5747; (d) Cozzi, P. G.; Solari, E.; Floriani, C.; Chiesi-Villa, A.; Pizzol, C. Chem. Ber. 1996, 129, 1361.
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Walker, M.A.1
Heathcock, C.H.2
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4 is increased due to its octahedral coordination. See: (a) Urabe, H.; Sato F. In Lewis Acids in Organic Synthesis; Yamamoto, H., Ed.; Wiley-VCH: Weinheim, 2000; Vol. 2; p. 653; (b) Shambayati, S.; Crowe, W. E.; Schreiber, S. L. Angew. Chem., Int. Ed. Engl. 1990, 29, 256; (c) Walker, M. A.; Heathcock, C. H. J. Org. Chem. 1991, 56, 5747; (d) Cozzi, P. G.; Solari, E.; Floriani, C.; Chiesi-Villa, A.; Pizzol, C. Chem. Ber. 1996, 129, 1361.
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Chem. Ber.
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Cozzi, P.G.1
Solari, E.2
Floriani, C.3
Chiesi-Villa, A.4
Pizzol, C.5
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