-
1
-
-
0035804384
-
Functionalized polymers-emerging versatile tools for solution-phase chemistry and automated parallel synthesis
-
Kirschning, A., Monenschein, H. and Wittenberg, R., Functionalized polymers-emerging versatile tools for solution-phase chemistry and automated parallel synthesis, Angew. Chem. Int. Ed. Engl., 40 (2001) 650-679.
-
(2001)
Angew. Chem. Int. Ed. Engl.
, vol.40
, pp. 650-679
-
-
Kirschning, A.1
Monenschein, H.2
Wittenberg, R.3
-
3
-
-
33748672334
-
Superbase catalysis of oxazolidin-2-one ring formation from carbondioxide and prop-2-yn-1-amines under homogeneous or heterogeneous conditions
-
Costa, M., Chiusoli, G., Taffurelli, D. and Dalmonego, G., Superbase catalysis of oxazolidin-2-one ring formation from carbondioxide and prop-2-yn-1-amines under homogeneous or heterogeneous conditions, J. Chem. Soc., Perkin Trans, 1, (1998) 1541-1546;
-
(1998)
J. Chem. Soc., Perkin Trans. 1
, pp. 1541-1546
-
-
Costa, M.1
Chiusoli, G.2
Taffurelli, D.3
Dalmonego, G.4
-
4
-
-
84962385340
-
Basicity of some organic superbases in acetonitrile
-
Kovacevic, B. and Maksic, Z.B., Basicity of some organic superbases in acetonitrile, Org. Lett., 3 (2001) 1523-1526.
-
(2001)
Org. Lett.
, vol.3
, pp. 1523-1526
-
-
Kovacevic, B.1
Maksic, Z.B.2
-
5
-
-
0034680561
-
Modified guanidines as potential chiral superbases. 1. Preparation of 1,3-disubstituted 2-iminoimidazolidines and the related guanidiens through chloroamidine derivatives
-
Isobe, T., Fukuda, K. and Ishikawa, T., Modified guanidines as potential chiral superbases. 1. Preparation of 1,3-disubstituted 2-iminoimidazolidines and the related guanidiens through chloroamidine derivatives, J. Org. Chem., 65 (2000) 7770-7773;
-
(2000)
J. Org. Chem.
, vol.65
, pp. 7770-7773
-
-
Isobe, T.1
Fukuda, K.2
Ishikawa, T.3
-
6
-
-
0034680659
-
Modified guanidines as potential chiral superbases. 2. Preparation of 1,3-unsubstituted and i-substituted 2-iminoimidazolidine derivatives and a related guanidiens by the 2-chloride-induced cyclization of thioureas
-
Isobe, T., Fukuda, K., Tokunaga, T., Seki, H., Yamaguchi, K. and Ishikawa, T., Modified guanidines as potential chiral superbases. 2. Preparation of 1,3-unsubstituted and i-substituted 2-iminoimidazolidine derivatives and a related guanidiens by the 2-chloride-induced cyclization of thioureas, J. Org. Chem., 65 (2000) 7774-7778;
-
(2000)
J. Org. Chem.
, vol.65
, pp. 7774-7778
-
-
Isobe, T.1
Fukuda, K.2
Tokunaga, T.3
Seki, H.4
Yamaguchi, K.5
Ishikawa, T.6
-
7
-
-
0034680580
-
Modified guanidines as potential chiral superbases. 3. Preparation of 1,4,6-triazabicyclooctene systems and 1,4-disubstituted 2-iminoimidazolidines by the 2-chloride-1,3-dimethylimidazolium chloride-induced cyclization of guanidines with a hydroxyethyl substituent
-
Isobe, T., Fukuda, K., Tokunaga, T., Seki, H., Yamaguchi, K. and Ishikawa, T., Modified guanidines as potential chiral superbases. 3. Preparation of 1,4,6-triazabicyclooctene systems and 1,4-disubstituted 2- iminoimidazolidines by the 2-chloride-1,3-dimethylimidazolium chloride-induced cyclization of guanidines with a hydroxyethyl substituent, J. Org. Chem., 65 (2000) 7779-7785.
-
(2000)
J. Org. Chem.
, vol.65
, pp. 7779-7785
-
-
Isobe, T.1
Fukuda, K.2
Tokunaga, T.3
Seki, H.4
Yamaguchi, K.5
Ishikawa, T.6
-
8
-
-
0035819594
-
Modified guanidines as chiral superbases: Application to asymmetric Michael reaction of glycine imine with acrylate or its related compounds
-
Ishikawa, T., Araki, Y., Kumamoto, T., Seki, H., Fukuda, K. and Isobe, T., Modified guanidines as chiral superbases: Application to asymmetric Michael reaction of glycine imine with acrylate or its related compounds, Chem. Commun., (2001) 245-246.
-
(2001)
Chem. Commun.
, pp. 245-246
-
-
Ishikawa, T.1
Araki, Y.2
Kumamoto, T.3
Seki, H.4
Fukuda, K.5
Isobe, T.6
-
9
-
-
0042495520
-
Umsetzungen α-metallierter isocyanide mit einigen 1,3-dipolen
-
Schoellkopf, U., Lau, H.H., Scheunemann, K.H., Blume, E. and Madawi-nata, K., Umsetzungen α-metallierter isocyanide mit einigen 1,3-dipolen, Liebigs Ann. Chem., (1980) 600-610.
-
(1980)
Liebigs Ann. Chem.
, pp. 600-610
-
-
Schoellkopf, U.1
Lau, H.H.2
Scheunemann, K.H.3
Blume, E.4
Madawi-Nata, K.5
-
10
-
-
0004777315
-
Synthesis of chiral N-and N,'substituted diamines and diamino alcohols from amino acids
-
Buono, G., Triantaphylides, C. and Peiffer, G., Synthesis of chiral N-and N,'substituted diamines and diamino alcohols from amino acids, Synthesis, (1982) 1030-1033.
-
(1982)
Synthesis
, pp. 1030-1033
-
-
Buono, G.1
Triantaphylides, C.2
Peiffer, G.3
-
11
-
-
0006517484
-
A new and efficient synthesis of 4-arylimidazolidin-2-ones
-
Rault, S., Tembo, O. N., Dallemagne, P. and Robba, M., A new and efficient synthesis of 4-arylimidazolidin-2-ones, Heterocycles, 32 (1991) 1301-1305.
-
(1991)
Heterocycles
, vol.32
, pp. 1301-1305
-
-
Rault, S.1
Tembo, O.N.2
Dallemagne, P.3
Robba, M.4
-
12
-
-
0027297238
-
Chiral oxazolidinones from N-Boc derivatives of β-amino alcohols. Effect of an N-methyl substituent on reactivity and stereochemistry
-
Agami, C., Cou-ty, F., Hamon, L. and Venier, O., Chiral oxazolidinones from N-Boc derivatives of β-amino alcohols. Effect of an N-methyl substituent on reactivity and stereochemistry, Tetrahedron Lett., 34 (1993) 4509-4512.
-
(1993)
Tetrahedron Lett.
, vol.34
, pp. 4509-4512
-
-
Agami, C.1
Cou-ty, F.2
Hamon, L.3
Venier, O.4
-
13
-
-
0008585811
-
The absolute configuration of (+)-1-methyl-2,6-diphenyl-4-piperidone oxime
-
Lyle, G. G. and Pelosi, E.T., The absolute configuration of (+)-1-methyl-2,6-diphenyl-4-piperidone oxime, J. Am. Chem. Soc., 88 (1966) 5276-5279.
-
(1966)
J. Am. Chem. Soc.
, vol.88
, pp. 5276-5279
-
-
Lyle, G.G.1
Pelosi, E.T.2
-
14
-
-
0001129359
-
Enantiospecific synthesis of a rigid, C2 symmetric, chiral guanidine by a new and direct method
-
Corey, E.J. and Otani, M., Enantiospecific synthesis of a rigid, C2 symmetric, chiral guanidine by a new and direct method, Tetrahedron Lett., 30 (1989) 5227-5230.
-
(1989)
Tetrahedron Lett.
, vol.30
, pp. 5227-5230
-
-
Corey, E.J.1
Otani, M.2
-
15
-
-
0033790635
-
A catalytic asymmetric Strecker-type reaction promoted by Lewis acid-Lewis base bifunctional catalyst
-
Takamura, M., Hamashima, Y., Usuda, H., Kanai, M. and Shibasaki, M., A catalytic asymmetric Strecker-type reaction promoted by Lewis acid-Lewis base bifunctional catalyst, Chem. Pharm. Bull., 48 (2000) 1586-1592.
-
(2000)
Chem. Pharm. Bull.
, vol.48
, pp. 1586-1592
-
-
Takamura, M.1
Hamashima, Y.2
Usuda, H.3
Kanai, M.4
Shibasaki, M.5
-
16
-
-
0037244721
-
Polymer-supported DMI as a potential heterogeneous dehydrating agent: Application to esterificationa and amidation
-
Wannaporn, D., Watanabe, T. and Ishikawa, T., Polymer-supported DMI as a potential heterogeneous dehydrating agent: Application to esterificationa and amidation, Synlett, (2003) 115-117.
-
(2003)
Synlett
, pp. 115-117
-
-
Wannaporn, D.1
Watanabe, T.2
Ishikawa, T.3
-
17
-
-
0035826551
-
New polymer-supported chiral phase-transfer catalysts in the asymmetric synthesis α-amino acids: The role of a spacer
-
Thierry, B., Plaquevent, J. C. and Cahard, D., New polymer-supported chiral phase-transfer catalysts in the asymmetric synthesis α-amino acids: The role of a spacer, Tetrahedron: Asymmetry, 12 (2001) 983-986.
-
(2001)
Tetrahedron: Asymmetry
, vol.12
, pp. 983-986
-
-
Thierry, B.1
Plaquevent, J.C.2
Cahard, D.3
-
18
-
-
0000542403
-
An efficient and versatile method for the synthesis of optically active 2-oxazolines: An acid-catalyzed condensation of ortho esters with amino acids
-
Kamata, K. and Agata, I., An efficient and versatile method for the synthesis of optically active 2-oxazolines: An acid-catalyzed condensation of ortho esters with amino acids, J. Org. Chem., 63 (1998), 3113-3116.
-
(1998)
J. Org. Chem.
, vol.63
, pp. 3113-3116
-
-
Kamata, K.1
Agata, I.2
-
19
-
-
0028111703
-
Synthesis of homochiral a-amino acids by reductive amination of α-ketoacids via 3-substituted-5-phenyl-3,4-dehydromorpholin-2-ones: Synthesis of (S)-and (R)-2-aminobutanoic acid
-
1994
-
Cox, G. G. and Harwood, L.M., Synthesis of homochiral a-amino acids by reductive amination of α-ketoacids via 3-substituted-5-phenyl-3,4- dehydromorpholin-2-ones: Synthesis of (S)-and (R)-2-aminobutanoic acid, Tetrahedron: Asymmetry, 5 (1994), 1669-1672 (1994).
-
(1994)
Tetrahedron: Asymmetry
, vol.5
, pp. 1669-1672
-
-
Cox, G.G.1
Harwood, L.M.2
-
20
-
-
0001036979
-
Enantioselective total synthesis of (+)-(S)-dihydroperiphylline
-
Kaseda, T., Kikuchi, T. and Kibayashi, C., Enantioselective total synthesis of (+)-(S)-dihydroperiphylline, Tetrahedron Lett., 30 (1998) 4539-4542.
-
(1998)
Tetrahedron Lett.
, vol.30
, pp. 4539-4542
-
-
Kaseda, T.1
Kikuchi, T.2
Kibayashi, C.3
-
21
-
-
0028286581
-
Inhibitors of acyl-CoA: Cholesterol O-acyl transferase (ACAT) as hypocholesterolemic agents. 8. Incorporation of amide or amine functionalities into a series of disubstituted ureas and carbamates. Effects on ACAT inhibition in vitro and efficacy in vivo
-
O'Brien, P. M., Sliskovic, D. R., Blankley, C. J., Roth, B. D. and Wilson, M. W., Inhibitors of acyl-CoA: cholesterol O-acyl transferase (ACAT) as hypocholesterolemic agents. 8. Incorporation of amide or amine functionalities into a series of disubstituted ureas and carbamates. Effects on ACAT inhibition in vitro and efficacy in vivo, J. Med. Chem., 37 (1994) 1810-1822.
-
(1994)
J. Med. Chem.
, vol.37
, pp. 1810-1822
-
-
O'Brien, P.M.1
Sliskovic, D.R.2
Blankley, C.J.3
Roth, B.D.4
Wilson, M.W.5
-
22
-
-
33751392709
-
New symmetric chiral dibenzyl- and diphenyl-substituted diamido-, dithioamido-, diaza-, and azapyridino-18-crown-6-ligands
-
Huszthy, P., Oue, M., Bradshaw, J.S., Zhu, C.Y. and Wang, T., New symmetric chiral dibenzyl- and diphenyl-substituted diamido-, dithioamido-, diaza-, and azapyridino-18-crown-6-ligands, J. Org. Chem., 57 (1992) 5383-5394.
-
(1992)
J. Org. Chem.
, vol.57
, pp. 5383-5394
-
-
Huszthy, P.1
Oue, M.2
Bradshaw, J.S.3
Zhu, C.Y.4
Wang, T.5
-
23
-
-
0023980281
-
Atropisomerism in polymers. Screw-sense selective polymerization of isocyanides by inhibiting the growth of one enantiomer of a racemic pair of helices
-
Kamer, P.C.J., Cleij, M.C., Nolte, R.J.M., Harada, T., Hezemans, A.M. F. and Drenth, W., Atropisomerism in polymers. Screw-sense selective polymerization of isocyanides by inhibiting the growth of one enantiomer of a racemic pair of helices, J. Am. Chem. Soc., 110 (1988) 1581-1587.
-
(1988)
J. Am. Chem. Soc.
, vol.110
, pp. 1581-1587
-
-
Kamer, P.C.J.1
Cleij, M.C.2
Nolte, R.J.M.3
Harada, T.4
Hezemans, A.M.F.5
Drenth, W.6
-
24
-
-
0031908520
-
A mild method for formylating amino esters without using any formylation agent
-
Giard, T., Benard, D. and Plaqueven, J.C., A mild method for formylating amino esters without using any formylation agent, Synthesis, (1998) 297-300.
-
(1998)
Synthesis
, pp. 297-300
-
-
Giard, T.1
Benard, D.2
Plaqueven, J.C.3
-
25
-
-
28344442913
-
Antifungal activities of α-isocyanoacetanilides
-
Takiguchi, K., Yamada, K., Suzuki, M., Nunami, K., Hayashi, K., Matsumoto, K., Antifungal activities of α-isocyanoacetanilides, Agric. Biol. Chem., 53 (1989) 69-76.
-
(1989)
Agric. Biol. Chem.
, vol.53
, pp. 69-76
-
-
Takiguchi, K.1
Yamada, K.2
Suzuki, M.3
Nunami, K.4
Hayashi, K.5
Matsumoto, K.6
|