-
1
-
-
0742324509
-
Chiral auxiliaries in polymer-supported organic synthesis
-
Chung, C.W.Y. & Toy, P.H. Chiral auxiliaries in polymer-supported organic synthesis. Tetrahedron: Asymmetry 15, 387-399 (2004
-
(2004)
Tetrahedron: Asymmetry
, vol.15
, pp. 387-399
-
-
Chung, C.W.Y.1
Toy, P.H.2
-
3
-
-
4744346554
-
Development of a solid-phase 'asymmetric resin-capture-releasé process: Application of an ephedrine chiral resin in an approach to γ-butyrolactones
-
Kerrigan, N.J., Hutchison, P.C., Heightman, T.D. & Procter, D.J. Development of a solid-phase 'asymmetric resin-capture-releasé process: Application of an ephedrine chiral resin in an approach to γ- butyrolactones. Org. Biomol. Chem. 2, 2476-2482 (2004
-
(2004)
Org. Biomol. Chem
, vol.2
, pp. 2476-2482
-
-
Kerrigan, N.J.1
Hutchison, P.C.2
Heightman, T.D.3
Procter, D.J.4
-
4
-
-
34248513143
-
Efficient dual catalytic enantioselective diethylzinc addition to the exocyclic C=N double bond of some 1,2,4-N-triazinylarylimines using polymer-supported chiral β-Amino alcohols derived from norephedrine
-
El-Shehawy, A.A. Efficient dual catalytic enantioselective diethylzinc addition to the exocyclic C=N double bond of some 1,2,4-N-triazinylarylimines using polymer-supported chiral β-Amino alcohols derived from norephedrine. Tetrahedron 63, 5490-5500 (2007
-
(2007)
Tetrahedron
, vol.63
, pp. 5490-5500
-
-
El-Shehawy, A.A.1
-
5
-
-
33947525013
-
Synthesis and evaluation of a new polymer-supported pseudoephedrine auxiliary for asymmetric alkylations on solid phase
-
McGhee, A.M., Kizirian, J.C. & Procter, D.J. Synthesis and evaluation of a new polymer-supported pseudoephedrine auxiliary for asymmetric alkylations on solid phase. Org. Biomol. Chem. 5, 1021-1024 (2007
-
(2007)
Org. Biomol. Chem
, vol.5
, pp. 1021-1024
-
-
McGhee, A.M.1
Kizirian, J.C.2
Procter, D.J.3
-
6
-
-
4644319268
-
Synthesis of a polymer-bound galactosylamine and its application as an immobilized chiral auxiliary in stereoselective syntheses of piperidine and amino acid derivatives
-
Zech, G. & Kunz, H. Synthesis of a polymer-bound galactosylamine and its application as an immobilized chiral auxiliary in stereoselective syntheses of piperidine and amino acid derivatives. Chem. Eur. J. 10, 4136-4149 (2004
-
(2004)
Chem. Eur. J.
, vol.10
, pp. 4136-4149
-
-
Zech, G.1
Kunz, H.2
-
7
-
-
18944373681
-
Dynamic kinetic resolution of α-chloro esters in asymmetric nucleophilic substitution using diacetone-d-glucose as a chiral auxiliary
-
Kim, H.J., Shin, E.K., Chang, J.Y., Kim, Y. & Park, Y.S. Dynamic kinetic resolution of α-chloro esters in asymmetric nucleophilic substitution using diacetone-d-glucose as a chiral auxiliary. Tetrahedron Lett. 46, 4115-4117 (2005
-
(2005)
Tetrahedron Lett
, vol.46
, pp. 4115-4117
-
-
Kim, H.J.1
Shin, E.K.2
Chang, J.Y.3
Kim, Y.4
Park, Y.S.5
-
8
-
-
26444468895
-
Chiral linker Part 2: Synthesis and evaluation of a novel, reusable solid-supported open chain chiral auxiliary derived from m-hydrobenzoin for the diastereoselective reduction of α-keto esters
-
Schuster, C., Knollmueller, M. & Gaertner, P. Chiral linker. Part 2: Synthesis and evaluation of a novel, reusable solid-supported open chain chiral auxiliary derived from m-hydrobenzoin for the diastereoselective reduction of α-keto esters. Tetrahedron: Asymmetry 16, 3211-3223 (2005
-
(2005)
Tetrahedron: Asymmetry
, vol.16
, pp. 3211-3223
-
-
Schuster, C.1
Knollmueller, M.2
Gaertner, P.3
-
9
-
-
33749247211
-
Chiral linker. Part 3: Synthesis and evaluation of aryl substituted m-hydrobenzoins as solid supported open chain chiral auxiliaries for the diastereoselective reduction of α-keto esters
-
Broeker, J., Knollmueller, M. & Gaertner, P. Chiral linker. Part 3: Synthesis and evaluation of aryl substituted m-hydrobenzoins as solid supported open chain chiral auxiliaries for the diastereoselective reduction of α-keto esters. Tetrahedron: Asymmetry 17, 2413-2429 (2006
-
(2006)
Tetrahedron: Asymmetry
, vol.17
, pp. 2413-2429
-
-
Broeker, J.1
Knollmueller, M.2
Gaertner, P.3
-
10
-
-
28044452665
-
Enantiopure sulfoxides and sulfinamides: Recent developments in their stereoselective synthesis and applications to asymmetric synthesis
-
Senanayake, C.H., Krishnamurthy, D., Lu, Z.H., Han, Z.X. & Gallou, I. Enantiopure sulfoxides and sulfinamides: Recent developments in their stereoselective synthesis and applications to asymmetric synthesis. Aldrichimica Acta. 38, 93-104 (2005
-
(2005)
Aldrichimica Acta
, vol.38
, pp. 93-104
-
-
Senanayake, C.H.1
Krishnamurthy, D.2
Lu, Z.H.3
Han, Z.X.4
Gallou, I.5
-
11
-
-
4544339940
-
Asymmetric synthesis of cycloalkenyl and alkenyloxiranes from allylic sulfoximines and aldehydes and application to solid-phase synthesis
-
Gais, H-J., Babu, G.S., Günter, M. & Das, P. Asymmetric synthesis of cycloalkenyl and alkenyloxiranes from allylic sulfoximines and aldehydes and application to solid-phase synthesis. Eur. J. Org. Chem. 1464-1473 (2004
-
(2004)
Eur. J. Org. Chem
, pp. 1464-1473
-
-
Gais, H.-J.1
Babu, G.S.2
Günter, M.3
Das, P.4
-
12
-
-
33645027432
-
Efficient remote axial-to-central chirality transfer in enantioselective Sml2-mediated reductive coupling of aldehydes with crotonates of atropisomeric 1-naphthamides
-
Zhang, Y., Wang, Y.Q. & Dai, W.M. Efficient remote axial-to-central chirality transfer in enantioselective Sml2-mediated reductive coupling of aldehydes with crotonates of atropisomeric 1-naphthamides. J. Org. Chem. 71, 2445-2455 (2006
-
(2006)
J. Org. Chem
, vol.71
, pp. 2445-2455
-
-
Zhang, Y.1
Wang, Y.Q.2
Dai, W.M.3
-
13
-
-
38349142808
-
Asymmetric diels-Alder reaction of aminodienes with a nonracemic acrylate bound to rink resin: A comparison of these reactions with their solution-state analogues
-
Songis, O., Geant, P.Y., Sautrey, G., Martinez, J. & Calmes, M. Asymmetric Diels-Alder reaction of aminodienes with a nonracemic acrylate bound to rink resin: A comparison of these reactions with their solution-state analogues. Eur. J. Org. Chem. 308-318 (2008
-
(2008)
Eur. J. Org. Chem
, pp. 308-318
-
-
Songis, O.1
Geant, P.Y.2
Sautrey, G.3
Martinez, J.4
Calmes, M.5
-
14
-
-
66049143012
-
Solid-phase asymmetric alkylation reactions using 2-imidazolidinone chiral auxiliary
-
Quynh, P.B.N., Kim, J.N. & Kim, T.H. Solid-phase asymmetric alkylation reactions using 2-imidazolidinone chiral auxiliary. Tetrahedron Lett. 50, 4015-4018 (2009
-
(2009)
Tetrahedron Lett
, vol.50
, pp. 4015-4018
-
-
Quynh, P.B.N.1
Kim, J.N.2
Kim, T.H.3
-
15
-
-
77949632348
-
N,N-Dialkylhydrazones in organic synthesis from simple N,N-dimethylhydrazones to supported chiral auxiliaries
-
Lazny, R. & Nodzewska, A. N,N-Dialkylhydrazones in organic synthesis. from simple N,N-dimethylhydrazones to supported chiral auxiliaries. Chem. Rev. 110, 1386-1434 (2009
-
(2009)
Chem. Rev
, vol.110
, pp. 1386-1434
-
-
Lazny, R.1
Nodzewska, A.2
-
16
-
-
0038468227
-
1,2-Amino alcohols and their heterocyclic derivatives as chiral auxiliaries in asymmetric synthesis
-
Ager, D.J., Prakash, I. & Schaad, D.R. 1,2-Amino alcohols and their heterocyclic derivatives as chiral auxiliaries in asymmetric synthesis. Chem. Rev. 96, 835-876 (1996
-
(1996)
Chem. Rev
, vol.96
, pp. 835-876
-
-
Ager, D.J.1
Prakash, I.2
Schaad, D.R.3
-
17
-
-
0030733231
-
Synthesis of chiral α-substituted β-hydroxy acid derivatives on solid support
-
Purandare, A.V. & Natarajan, S. Synthesis of chiral α-substituted β-hydroxy acid derivatives on solid support. Tetrahedron Lett. 38, 8777-8780 (1997
-
(1997)
Tetrahedron Lett
, vol.38
, pp. 8777-8780
-
-
Purandare, A.V.1
Natarajan, S.2
-
18
-
-
0000680330
-
Resin type can have important effects on solid phase asymmetric alkylation reactions
-
Burgess, K. & Lim, D. Resin type can have important effects on solid phase asymmetric alkylation reactions. Chem. Commun. 785-786 (1997
-
(1997)
Chem. Commun
, pp. 785-786
-
-
Burgess, K.1
Lim, D.2
-
19
-
-
0032500099
-
Diels-Alder reaction on solid supports using polymer-bound oxazolidinones
-
Winkler, J.D. & McCoull, W. Diels-Alder reaction on solid supports using polymer-bound oxazolidinones. Tetrahedron Lett. 39, 4935-4936 (1998
-
(1998)
Tetrahedron Lett
, vol.39
, pp. 4935-4936
-
-
Winkler, J.D.1
McCoull, W.2
-
20
-
-
0035944167
-
Solid supported chiral auxiliaries in asymmetric synthesis part 2: Catalysis of 1,3-dipolar cycloadditions by mg(ii) cation
-
Faita, G., Paio, A., Quadrelli, P., Rancati, F. & Seneci, P. Solid supported chiral auxiliaries in asymmetric synthesis. Part 2: Catalysis of 1,3-dipolar cycloadditions by Mg(II) cation. Tetrahedron 57, 8313-8322 (2001
-
(2001)
Tetrahedron
, vol.57
, pp. 8313-8322
-
-
Faita, G.1
Paio, A.2
Quadrelli, P.3
Rancati, F.4
Seneci, P.5
-
21
-
-
0034685257
-
4S)-p-Hydroxybenzyl-1,3-oxazolidin-2-one as a solid-supported chiral auxiliary in asymmetric 1,3-dipolar cycloadditions
-
Faita, G., Paio, A., Quadrelli, P., Rancati, F. & Seneci, P. (4S)-p-Hydroxybenzyl-1,3-oxazolidin-2-one as a solid-supported chiral auxiliary in asymmetric 1,3-dipolar cycloadditions. Tetrahedron Lett. 41, 1265-1269 (2000
-
(2000)
Tetrahedron Lett
, vol.41
, pp. 1265-1269
-
-
Faita, G.1
Paio, A.2
Quadrelli, P.3
Rancati, F.4
Seneci, P.5
-
22
-
-
15044359102
-
Design and synthesis of a new polymer-supported Evans-type oxazolidinone: An efficient chiral auxiliary in the solid-phase asymmetric alkylation reactions
-
Kotake, T. et al. Design and synthesis of a new polymer-supported Evans-type oxazolidinone: An efficient chiral auxiliary in the solid-phase asymmetric alkylation reactions. Tetrahedron 61, 3819-3833 (2005
-
(2005)
Tetrahedron
, vol.61
, pp. 3819-3833
-
-
Kotake, T.1
-
23
-
-
0032560075
-
Solid phase aldol and conjugate addition reactions using Evans' oxazolidinone chiral auxiliary
-
Phoon, C.W. & Abell, C. Solid phase aldol and conjugate addition reactions using Evans' oxazolidinone chiral auxiliary. Tetrahedron Lett. 39, 2655-2658 (1998
-
(1998)
Tetrahedron Lett
, vol.39
, pp. 2655-2658
-
-
Phoon, C.W.1
Abell, C.2
-
24
-
-
67649491241
-
Efficient asymmetric synthesis of chiral hydroxy-γ-butyrolactones
-
Davies, I.R. et al. Efficient asymmetric synthesis of chiral hydroxy-γ-butyrolactones. Org. Lett. 11, 2896-2899 (2009
-
(2009)
Org. Lett
, vol.11
, pp. 2896-2899
-
-
Davies, I.R.1
-
25
-
-
38049178422
-
A cleavable linker strategy for optimising enolate alkylation reactions of a polymer-supported Evans' oxazolidin-2-one
-
Green, R., Merritt, A.T. & Bull, S.D. A cleavable linker strategy for optimising enolate alkylation reactions of a polymer-supported Evans' oxazolidin-2-one. Chem. Commun. 508-510 (2008
-
(2008)
Chem. Commun
, pp. 508-510
-
-
Green, R.1
Merritt, A.T.2
Bull, S.D.3
-
26
-
-
0037010828
-
Solution-And solid-phase synthesis of enantiomerically pure spiro oxindoles
-
Ganguly, A.K. et al. Solution-And solid-phase synthesis of enantiomerically pure spiro oxindoles. Tetrahedron Lett. 43, 8981-8983 (2002
-
(2002)
Tetrahedron Lett
, vol.43
, pp. 8981-8983
-
-
Ganguly, A.K.1
-
27
-
-
42449161962
-
An oxidatively-Activated safety-catch linker for solid-phase synthesis
-
Davies, S.G. et al. An oxidatively-Activated safety-catch linker for solid-phase synthesis. Org. Biomol. Chem. 6, 1625-1634 (2008
-
(2008)
Org. Biomol. Chem
, vol.6
, pp. 1625-1634
-
-
Davies, S.G.1
-
28
-
-
78249255226
-
A new non-cross-linked polystyrene supported 2-phenylimino-2-oxazolidine chiral auxiliary: Synthesis and application in asymmetric alkylation reactions
-
Hu, F-Q., Xia, D-X., Lu, C-F., Chen, Z-X. & Yang, G-C. A new non-cross-linked polystyrene supported 2-phenylimino-2-oxazolidine chiral auxiliary: Synthesis and application in asymmetric alkylation reactions. Eur. J. Org. Chem. 2010, 5552-5554 (2010
-
(2010)
Eur. J. Org. Chem
, vol.2010
, pp. 5552-5554
-
-
Hu, F.-Q.1
Xia, D.-X.2
Lu, C.-F.3
Chen, Z.-X.4
Yang, G.-C.5
-
29
-
-
61849125183
-
Stereoselective synthesis of sex pheromone (R)-4-methyl-1-nonanol: Non-cross-linked polystyrene supported oxazolidinone as a chiral auxiliary
-
Lu, C., Li, D., Wang, Q., Yang, G. & Chen, Z. Stereoselective synthesis of sex pheromone (R)-4-methyl-1-nonanol: Non-cross-linked polystyrene supported oxazolidinone as a chiral auxiliary. Eur. J. Org. Chem. 1078-1081 (2009
-
(2009)
Eur. J. Org. Chem
, pp. 1078-1081
-
-
Lu, C.1
Li, D.2
Wang, Q.3
Yang, G.4
Chen, Z.5
-
30
-
-
0037155701
-
A soluble polymer-bound evans' chiral auxiliary: Syn thesis characterization and use in cycloaddition reactions
-
Desimoni, G. et al. A soluble polymer-bound Evans' chiral auxiliary: Synthesis, characterization and use in cycloaddition reactions. Tetrahedron: Asymmetry 13, 333-337 (2002
-
(2002)
Tetrahedron: Asymmetry
, vol.13
, pp. 333-337
-
-
Desimoni, G.1
-
31
-
-
0000911225
-
An improved preparation of oxazolidin-2-one chiral auxiliaries
-
Sudharshan, M. & Hultin, P.G. An improved preparation of oxazolidin-2-one chiral auxiliaries. Synlett 171-172 (1997
-
(1997)
Synlett
, pp. 171-172
-
-
Sudharshan, M.1
Hultin, P.G.2
-
32
-
-
0041830946
-
A practical synthesis of enantiopure (S)-4-(4-hydroxybenzyl)-oxazolidin- 2-one
-
Green, R. et al. A practical synthesis of enantiopure (S)-4-(4-hydroxybenzyl)-oxazolidin-2-one. Tetrahedron: Asymmetry 14, 2619-2623 (2003
-
(2003)
Tetrahedron: Asymmetry
, vol.14
, pp. 2619-2623
-
-
Green, R.1
-
33
-
-
77953202473
-
Preparation and supporting on solid phase of chiral auxiliary (S)-4-(4-hydroxybenzyl)oxazolidin-2-one from l-tyrosinol assisted by microwaves
-
Cruz, A. & Rivero, I.A. Preparation and supporting on solid phase of chiral auxiliary (S)-4-(4-hydroxybenzyl)oxazolidin-2-one from l-tyrosinol assisted by microwaves. J. Mex. Chem. Soc. 53, 120-125 (2009
-
(2009)
J. Mex. Chem. Soc
, vol.53
, pp. 120-125
-
-
Cruz, A.1
Rivero, I.A.2
-
34
-
-
0030889523
-
Efficient synthesis of selectively protected l-dopa derivatives from l-Tyrosine via Reimer-Tiemann and Dakin reactions
-
Jung, M.E. & Lazarova, T.I. Efficient synthesis of selectively protected l-dopa derivatives from l-Tyrosine via Reimer-Tiemann and Dakin reactions. J. Org. Chem. 62, 1553-1555 (1997
-
(1997)
J. Org. Chem
, vol.62
, pp. 1553-1555
-
-
Jung, M.E.1
Lazarova, T.I.2
-
35
-
-
0033407595
-
Enantioselective allylic alkylation using polymer-supported palladium catalysts
-
Hallman, K., Macedo, E., Nordström, K. & Moberg, C. Enantioselective allylic alkylation using polymer-supported palladium catalysts. Tetrahedron: Asymmetry 10, 4037-4046 (1999
-
(1999)
Tetrahedron: Asymmetry
, vol.10
, pp. 4037-4046
-
-
Hallman, K.1
Macedo, E.2
Nordström, K.3
Moberg, C.4
-
36
-
-
36348939278
-
A temporary stereocentre approach for the stereodivergent synthesis of either enantiomer of α-methyloctanal
-
Niyadurupola, D.G., Davies, I.R., Wisedale, R. & Bull, S.D. A temporary stereocentre approach for the stereodivergent synthesis of either enantiomer of α-methyloctanal. Eur. J. Org. Chem. 5487-5491 (2007
-
(2007)
Eur. J. Org. Chem
, pp. 5487-5491
-
-
Niyadurupola, D.G.1
Davies, I.R.2
Wisedale, R.3
Bull, S.D.4
-
37
-
-
78149281157
-
An expedient asymmetric synthesis of N-protected (S,S)-2-Aminomethyl-1- cyclopropanecarboxylic acid
-
Aitken, D.J. et al. An expedient asymmetric synthesis of N-protected (S,S)-2-Aminomethyl-1-cyclopropanecarboxylic acid. Synlett 2729-2732 (2010
-
(2010)
Synlett
, pp. 2729-2732
-
-
Aitken, D.J.1
-
38
-
-
33646568495
-
An efficient asymmetric synthesis of cascarillic acid
-
Cheeseman, M. & Bull, S.D. An efficient asymmetric synthesis of cascarillic acid. Synlett 7, 1119-1121 (2006
-
(2006)
Synlett
, vol.7
, pp. 1119-1121
-
-
Cheeseman, M.1
Bull, S.D.2
-
39
-
-
70349298428
-
A temporary stereocentre approach for the asymmetric synthesis of chiral cyclopropane-carboxaldehydes
-
Cheeseman, M., Davies, I.R., Axe, P., Johnson, A.L. & Bull, S.D. A temporary stereocentre approach for the asymmetric synthesis of chiral cyclopropane-carboxaldehydes. Org. Biomol. Chem. 7, 3537-3548 (2009
-
(2009)
Org. Biomol. Chem
, vol.7
, pp. 3537-3548
-
-
Cheeseman, M.1
Davies, I.R.2
Axe, P.3
Johnson, A.L.4
Bull, S.D.5
-
40
-
-
19944381888
-
A novel strategy for the asymmetric synthesis of chiral cyclopropane carboxaldehydes
-
Cheeseman, M., Feuillet, F.J.P., Johnson, A.L. & Bull, S.D. A novel strategy for the asymmetric synthesis of chiral cyclopropane carboxaldehydes. Chem. Commun. 2372-2374 (2005
-
(2005)
Chem. Commun
, pp. 2372-2374
-
-
Cheeseman, M.1
Feuillet, F.J.P.2
Johnson, A.L.3
Bull, S.D.4
-
41
-
-
22144484527
-
An efficient synthesis of semiplenamide C
-
Davies, I.R., Cheeseman, M., Niyadurupola, D.G. & Bull, S.D. An efficient synthesis of semiplenamide C. Tetrahedron Lett. 46, 5547-5549 (2005
-
(2005)
Tetrahedron Lett
, vol.46
, pp. 5547-5549
-
-
Davies, I.R.1
Cheeseman, M.2
Niyadurupola, D.G.3
Bull, S.D.4
-
42
-
-
26844501274
-
An efficient asymmetric synthesis of grenadamide
-
Green, R., Cheeseman, M., Duffill, S., Merritt, A. & Bull, S.D. An efficient asymmetric synthesis of grenadamide. Tetrahedron Lett. 46, 7931-7934 (2005
-
(2005)
Tetrahedron Lett
, vol.46
, pp. 7931-7934
-
-
Green, R.1
Cheeseman, M.2
Duffill, S.3
Merritt, A.4
Bull, S.D.5
-
43
-
-
79960154365
-
Asymmetric synthesis of chiral δ-lactones containing multiple contiguous stereocenters
-
Peed, J. et al. Asymmetric synthesis of chiral δ-lactones containing multiple contiguous stereocenters. Org. Lett. 13, 3592-3595 (2011
-
(2011)
Org. Lett
, vol.13
, pp. 3592-3595
-
-
Peed, J.1
-
44
-
-
84855544324
-
Dihydroxylation-based approach for the asymmetric syntheses of hydroxy-γ-butyrolactones
-
Peed, J. et al. Dihydroxylation-based approach for the asymmetric syntheses of hydroxy-γ-butyrolactones. J. Org. Chem. 77, 543-555 (2012
-
(2012)
J. Org. Chem
, vol.77
, pp. 543-555
-
-
Peed, J.1
-
45
-
-
0000604671
-
Acyclic stereoselection 48 Reversal of stereochemistry in the aldol reactions of a chiral boron enolate
-
Danda, H., Hansen, M.M. & Heathcock, C.H. Acyclic stereoselection. 48. Reversal of stereochemistry in the aldol reactions of a chiral boron enolate. J. Org. Chem. 55, 173-181 (1990
-
(1990)
J. Org. Chem
, vol.55
, pp. 173-181
-
-
Danda, H.1
Hansen, M.M.2
Heathcock, C.H.3
-
46
-
-
0001071065
-
Lithium-initiated imide formation A simple method for N-Acylation of 2-oxazolidinones and bornane-2,10-sultam
-
Ho, G-J. & Mathre, D.J. Lithium-initiated imide formation. A simple method for N-Acylation of 2-oxazolidinones and bornane-2,10-sultam. J. Org. Chem. 60, 2271-2273 (1995
-
(1995)
J. Org. Chem
, vol.60
, pp. 2271-2273
-
-
Ho, G.-J.1
Mathre, D.J.2
-
47
-
-
0004936902
-
Peptide synthesis in aqueous solution 5 Properties and reactivities of (p-hydroxyphenyl)benzylmethylsulfonium salts for direct benzyl esterification of N-Acylpeptides
-
Nakata, T. et al. Peptide synthesis in aqueous solution. 5. Properties and reactivities of (p-hydroxyphenyl)benzylmethylsulfonium salts for direct benzyl esterification of N-Acylpeptides. Bull. Chem. Soc. Jpn. 69, 1099-1106 (1996
-
(1996)
Bull. Chem. Soc. Jpn
, vol.69
, pp. 1099-1106
-
-
Nakata, T.1
-
48
-
-
0023250889
-
New approaches to the synthesis of trans-Alkene isosteres of dipeptides
-
Spaltenstein, A., Carpino, P.A., Miyake, F. & Hopkins, P.B. New approaches to the synthesis of trans-Alkene isosteres of dipeptides. J. Org. Chem. 52, 3759-3766 (1987
-
(1987)
J. Org. Chem
, vol.52
, pp. 3759-3766
-
-
Spaltenstein, A.1
Carpino, P.A.2
Miyake, F.3
Hopkins, P.B.4
-
49
-
-
0344137670
-
Protocols for the preparation of each of the four possible stereoisomeric α-Alkyl-β-hydroxy carboxylic acids from a single chiral aldol reagent
-
Vandraanen, N.A., Arseniyadis, S., Crimmins, M.T. & Heathcock, C.H. Protocols for the preparation of each of the four possible stereoisomeric α-Alkyl-β-hydroxy carboxylic acids from a single chiral aldol reagent. J. Org. Chem. 56, 2499-2506 (1991
-
(1991)
J. Org. Chem
, vol.56
, pp. 2499-2506
-
-
Vandraanen, N.A.1
Arseniyadis, S.2
Crimmins, M.T.3
Heathcock, C.H.4
-
50
-
-
78149280506
-
Cyclosulfamide as a chiral auxiliary: Application to efficient asymmetric syn thesis alkylation/aldolization
-
Fécourt, F., Lopez, G., Van Der Lee, A., Martinez, J. & Dewynter, G. Cyclosulfamide as a chiral auxiliary: Application to efficient asymmetric synthesis (alkylation/aldolization). Tetrahedron: Asymmetry 21, 2361-2366 (2010
-
(2010)
Tetrahedron: Asymmetry
, vol.21
, pp. 2361-2366
-
-
Fécourt, F.1
Lopez, G.2
Van Der Lee, A.3
Martinez, J.4
Dewynter, G.5
-
51
-
-
0037025732
-
Chelation-controlled ester-derived titanium enolate aldol reaction: Diastereoselective syn-Aldols with mono-And bidentate aldehydes
-
Ghosh, A.K. & Kim, J.H. Chelation-controlled ester-derived titanium enolate aldol reaction: Diastereoselective syn-Aldols with mono-And bidentate aldehydes. Tetrahedron Lett. 43, 5621-5624 (2002
-
(2002)
Tetrahedron Lett
, vol.43
, pp. 5621-5624
-
-
Ghosh, A.K.1
Kim, J.H.2
|