-
1
-
-
48249132560
-
Asymmetric organocatalysis
-
Jaroch, S.; Weinmann, H.; Zeitler, K. Asymmetric organocatalysis Chem. Med. Chem. 2007, 2, 1261-1264
-
(2007)
Chem. Med. Chem.
, vol.2
, pp. 1261-1264
-
-
Jaroch, S.1
Weinmann, H.2
Zeitler, K.3
-
4
-
-
0001564142
-
Recent advances in the measurement of enantiomeric excesses
-
Tsukamoto, M.; Kagan, H. B. Recent advances in the measurement of enantiomeric excesses Adv. Synth. Catal. 2002, 344, 453-463
-
(2002)
Adv. Synth. Catal.
, vol.344
, pp. 453-463
-
-
Tsukamoto, M.1
Kagan, H.B.2
-
5
-
-
0036084211
-
Emerging methods for the rapid determination of enantiomeric excess
-
Finn, M. G. Emerging methods for the rapid determination of enantiomeric excess Chirality 2002, 14, 534-540
-
(2002)
Chirality
, vol.14
, pp. 534-540
-
-
Finn, M.G.1
-
6
-
-
0031561759
-
Some recent high-performance liquid chromatography separations of the enantiomers of pharmaceuticals and other compounds using the Whelk-O 1 chiral stationary phase
-
Welch, C. J.; Szczerba, T.; Perrin, S. R. Some recent high-performance liquid chromatography separations of the enantiomers of pharmaceuticals and other compounds using the Whelk-O 1 chiral stationary phase J. Chromatogr. A 1997, 758, 93-98
-
(1997)
J. Chromatogr. A
, vol.758
, pp. 93-98
-
-
Welch, C.J.1
Szczerba, T.2
Perrin, S.R.3
-
7
-
-
0035812734
-
Use of chiral HPLC-MS for rapid evaluation of the yeast-mediated enantioselective bioreduction of a diaryl ketone
-
Welch, C. J.; Grau, B.; Moore, J.; Mathre, D. J. Use of chiral HPLC-MS for rapid evaluation of the yeast-mediated enantioselective bioreduction of a diaryl ketone J. Org. Chem. 2001, 66, 6836-6837
-
(2001)
J. Org. Chem.
, vol.66
, pp. 6836-6837
-
-
Welch, C.J.1
Grau, B.2
Moore, J.3
Mathre, D.J.4
-
8
-
-
1842506638
-
Chromatography as an enabling technology in pharmaceutical process development: Expedited multikilogram preparation of a candidate HIV protease inhibitor
-
Welch, C. J.; Fleitz, F.; Antia, F.; Yehl, P. Chromatography as an enabling technology in pharmaceutical process development: Expedited multikilogram preparation of a candidate HIV protease inhibitor Org. Process Res. Dev. 2004, 8, 186-191
-
(2004)
Org. Process Res. Dev.
, vol.8
, pp. 186-191
-
-
Welch, C.J.1
Fleitz, F.2
Antia, F.3
Yehl, P.4
-
9
-
-
0003554758
-
Schiff base catalysts for the asymmetric Strecker reaction identified and optimized from parallel synthetic libraries
-
Sigman, M. S.; Jacobsen, E. N. Schiff base catalysts for the asymmetric Strecker reaction identified and optimized from parallel synthetic libraries J. Am. Chem. Soc. 1998, 120, 4901-4902
-
(1998)
J. Am. Chem. Soc.
, vol.120
, pp. 4901-4902
-
-
Sigman, M.S.1
Jacobsen, E.N.2
-
10
-
-
0037134205
-
A high-throughput screening protocol for fast evaluation of enantioselective catalysts
-
Wolf, C.; Hawes, P. A. A high-throughput screening protocol for fast evaluation of enantioselective catalysts J. Org. Chem. 2002, 67, 2727-2729
-
(2002)
J. Org. Chem.
, vol.67
, pp. 2727-2729
-
-
Wolf, C.1
Hawes, P.A.2
-
11
-
-
1842430722
-
Fluorescence of organic molecules in chiral recognition
-
Pu, L. Fluorescence of organic molecules in chiral recognition Chem. Rev. 2004, 104, 1687-1716
-
(2004)
Chem. Rev.
, vol.104
, pp. 1687-1716
-
-
Pu, L.1
-
12
-
-
84878649427
-
Chirality sensing using stereodynamic probes with distinct electronic circular dichroism output
-
Wolf, C.; Bentley, K. W. Chirality sensing using stereodynamic probes with distinct electronic circular dichroism output Chem. Soc. Rev. 2013, 42, 5408-5424
-
(2013)
Chem. Soc. Rev.
, vol.42
, pp. 5408-5424
-
-
Wolf, C.1
Bentley, K.W.2
-
13
-
-
84883070053
-
Stereodynamic chemosensor with selective circular dichroism and fluorescence readout for in situ determination of absolute configuration, enantiomeric excess, and concentration of chiral compounds
-
Bentley, K. W.; Wolf, C. Stereodynamic chemosensor with selective circular dichroism and fluorescence readout for in situ determination of absolute configuration, enantiomeric excess, and concentration of chiral compounds J. Am. Chem. Soc. 2013, 135, 12200-12203
-
(2013)
J. Am. Chem. Soc.
, vol.135
, pp. 12200-12203
-
-
Bentley, K.W.1
Wolf, C.2
-
14
-
-
1642404953
-
Facile quantification of enantiomeric excess and concentration with indicator-displacement assays: An example in the analyses of alpha-hydroxyacids
-
Zhu, L.; Anslyn, E. V. Facile quantification of enantiomeric excess and concentration with indicator-displacement assays: an example in the analyses of alpha-hydroxyacids J. Am. Chem. Soc. 2004, 126, 3676-3677
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 3676-3677
-
-
Zhu, L.1
Anslyn, E.V.2
-
15
-
-
16244420077
-
Guidelines in implementing enantioselective indicator-displacement assays for alpha-hydroxycarboxylates and diols
-
Zhu, L.; Zhong, Z.; Anslyn, E. V. Guidelines in implementing enantioselective indicator-displacement assays for alpha-hydroxycarboxylates and diols J. Am. Chem. Soc. 2005, 127, 4260-4269
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 4260-4269
-
-
Zhu, L.1
Zhong, Z.2
Anslyn, E.V.3
-
16
-
-
33845941522
-
Two methods for the determination of enantiomeric excess and concentration of a chiral sample with a single spectroscopic measurement
-
Zhu, L.; Shabbir, S. H.; Anslyn, E. V. Two methods for the determination of enantiomeric excess and concentration of a chiral sample with a single spectroscopic measurement Chem.-Eur. J. 2007, 13, 99-104
-
(2007)
Chem.-Eur. J.
, vol.13
, pp. 99-104
-
-
Zhu, L.1
Shabbir, S.H.2
Anslyn, E.V.3
-
17
-
-
70349146708
-
Pattern-based recognition for the rapid determination of identity, concentration, and enantiomeric excess of subtly different threo diols
-
Shabbir, S. H.; Joyce, L. A.; da Cruz, G. M.; Lynch, V. M.; Sorey, S.; Anslyn, E. V. Pattern-based recognition for the rapid determination of identity, concentration, and enantiomeric excess of subtly different threo diols J. Am. Chem. Soc. 2009, 131, 13125-13131
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 13125-13131
-
-
Shabbir, S.H.1
Joyce, L.A.2
Da Cruz, G.M.3
Lynch, V.M.4
Sorey, S.5
Anslyn, E.V.6
-
18
-
-
67649795138
-
A general protocol for creating high-throughput screening assays for reaction yield and enantiomeric excess applied to hydrobenzoin
-
Shabbir, S. H.; Regan, C. J.; Anslyn, E. V. A general protocol for creating high-throughput screening assays for reaction yield and enantiomeric excess applied to hydrobenzoin Proc. Natl. Acad. Sci. U.S.A. 2009, 106, 10487
-
(2009)
Proc. Natl. Acad. Sci. U.S.A.
, vol.106
, pp. 10487
-
-
Shabbir, S.H.1
Regan, C.J.2
Anslyn, E.V.3
-
19
-
-
20444413104
-
Colorimetric enantiodiscrimination of alpha-amino acids in protic media
-
Folmer-Andersen, J. F.; Lynch, V. M.; Anslyn, E. V. Colorimetric enantiodiscrimination of alpha-amino acids in protic media J. Am. Chem. Soc. 2005, 127, 7986-7987
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 7986-7987
-
-
Folmer-Andersen, J.F.1
Lynch, V.M.2
Anslyn, E.V.3
-
20
-
-
33646575600
-
Pattern-based discrimination of enantiomeric and structurally similar amino acids: An optical mimic of the mammalian taste response
-
Folmer-Andersen, J. F.; Kitamura, M.; Anslyn, E. V. Pattern-based discrimination of enantiomeric and structurally similar amino acids: an optical mimic of the mammalian taste response J. Am. Chem. Soc. 2006, 128, 5652-5653
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 5652-5653
-
-
Folmer-Andersen, J.F.1
Kitamura, M.2
Anslyn, E.V.3
-
21
-
-
51949091374
-
Using enantioselective indicator displacement assays to determine the enantiomeric excess of alpha-amino acids
-
Leung, D.; Folmer-Andersen, J. F.; Lynch, V. M.; Anslyn, E. V. Using enantioselective indicator displacement assays to determine the enantiomeric excess of alpha-amino acids J. Am. Chem. Soc. 2008, 130, 12318-12327
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 12318-12327
-
-
Leung, D.1
Folmer-Andersen, J.F.2
Lynch, V.M.3
Anslyn, E.V.4
-
22
-
-
51949110385
-
Transitioning enantioselective indicator displacement assays for α-amino acids to protocols amenable to high-throughput screening
-
Leung, D.; Anslyn, E. V. Transitioning enantioselective indicator displacement assays for α-amino acids to protocols amenable to high-throughput screening J. Am. Chem. Soc. 2008, 130, 12328-12333
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 12328-12333
-
-
Leung, D.1
Anslyn, E.V.2
-
23
-
-
33947546305
-
Optimization by statistical linear discriminant analysis in analytical chemistry
-
Coomans, D.; Massart, D. L.; Kaufman, L. Optimization by statistical linear discriminant analysis in analytical chemistry Anal. Chim. Acta 1979, 112, 97-122
-
(1979)
Anal. Chim. Acta
, vol.112
, pp. 97-122
-
-
Coomans, D.1
Massart, D.L.2
Kaufman, L.3
-
24
-
-
0008466488
-
Robust linear discriminant analysis for chemical pattern recognition
-
Li, Y.; Jiang, J. H.; Chen, Z. P.; Xu, C. J. Robust linear discriminant analysis for chemical pattern recognition J. Chemom. 1999, 13, 3-13
-
(1999)
J. Chemom.
, vol.13
, pp. 3-13
-
-
Li, Y.1
Jiang, J.H.2
Chen, Z.P.3
Xu, C.J.4
-
25
-
-
40449141013
-
What is principal component analysis?
-
Ringnér, M. What is principal component analysis? Nat. Biotechnol. 2008, 26, 303-304
-
(2008)
Nat. Biotechnol.
, vol.26
, pp. 303-304
-
-
Ringnér, M.1
-
26
-
-
47749111758
-
High-throughput screening of identity, enantiomeric excess, and concentration using MLCT transitions in CD spectroscopy
-
Nieto, S.; Lynch, V. M.; Anslyn, E. V.; Kim, H. High-throughput screening of identity, enantiomeric excess, and concentration using MLCT transitions in CD spectroscopy J. Am. Chem. Soc. 2008, 130, 9232-9233
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 9232-9233
-
-
Nieto, S.1
Lynch, V.M.2
Anslyn, E.V.3
Kim, H.4
-
27
-
-
58149196462
-
Rapid enantiomeric excess and concentration determination using simple racemic metal complexes
-
Nieto, S.; Lynch, V. M.; Anslyn, E. V.; Kim, H.; Chin, J. Rapid enantiomeric excess and concentration determination using simple racemic metal complexes Org. Lett. 2008, 10, 5167-5170
-
(2008)
Org. Lett.
, vol.10
, pp. 5167-5170
-
-
Nieto, S.1
Lynch, V.M.2
Anslyn, E.V.3
Kim, H.4
Chin, J.5
-
28
-
-
84864966808
-
Vibrational circular dichroism spectroscopy of two chiral binaphthyl diphosphine ligands and their palladium complexes in solution
-
Dezhahang, Z.; Merten, C.; Poopari, M. R.; Xu, Y. Vibrational circular dichroism spectroscopy of two chiral binaphthyl diphosphine ligands and their palladium complexes in solution Dalton Trans. 2012, 41, 10817-10824
-
(2012)
Dalton Trans.
, vol.41
, pp. 10817-10824
-
-
Dezhahang, Z.1
Merten, C.2
Poopari, M.R.3
Xu, Y.4
-
29
-
-
73949101129
-
A facile circular dichroism protocol for rapid determination of enantiomeric excess and concentration of chiral primary amines
-
Nieto, S.; Dragna, J. M.; Anslyn, E. V. A facile circular dichroism protocol for rapid determination of enantiomeric excess and concentration of chiral primary amines Chem.-Eur. J. 2010, 16, 227-232
-
(2010)
Chem.-Eur. J.
, vol.16
, pp. 227-232
-
-
Nieto, S.1
Dragna, J.M.2
Anslyn, E.V.3
-
30
-
-
79955638488
-
Rapid determination of enantiomeric excess of α-chiral cyclohexanones using circular dichroism spectroscopy
-
Leung, D.; Anslyn, E. V. Rapid determination of enantiomeric excess of α-chiral cyclohexanones using circular dichroism spectroscopy Org. Lett. 2011, 13, 2298-2301
-
(2011)
Org. Lett.
, vol.13
, pp. 2298-2301
-
-
Leung, D.1
Anslyn, E.V.2
-
31
-
-
84857848611
-
In situ assembly of octahedral Fe(II) complexes for the enantiomeric excess determination of chiral amines using circular dichroism spectroscopy
-
Dragna, J. M.; Pescitelli, G.; Tran, L.; Lynch, V. M.; Anslyn, E. V.; Di Bari, L. In situ assembly of octahedral Fe(II) complexes for the enantiomeric excess determination of chiral amines using circular dichroism spectroscopy J. Am. Chem. Soc. 2012, 134, 4398-4407
-
(2012)
J. Am. Chem. Soc.
, vol.134
, pp. 4398-4407
-
-
Dragna, J.M.1
Pescitelli, G.2
Tran, L.3
Lynch, V.M.4
Anslyn, E.V.5
Di Bari, L.6
-
32
-
-
33644773399
-
Simple protocol for NMR analysis of the enantiomeric purity of primary amines
-
Pérez-Fuertes, Y.; Kelly, A. M.; Johnson, A. L.; Arimori, S.; Bull, S. D.; James, T. D. Simple protocol for NMR analysis of the enantiomeric purity of primary amines Org. Lett. 2006, 8, 609-612
-
(2006)
Org. Lett.
, vol.8
, pp. 609-612
-
-
Pérez-Fuertes, Y.1
Kelly, A.M.2
Johnson, A.L.3
Arimori, S.4
Bull, S.D.5
James, T.D.6
-
33
-
-
39449139629
-
Simple protocols for NMR analysis of the enantiomeric purity of chiral primary amines
-
Pérez-Fuertes, Y.; Kelly, A. M.; Fossey, J. S.; Powell, M. E.; Bull, S. D.; James, T. D. Simple protocols for NMR analysis of the enantiomeric purity of chiral primary amines Nat. Protoc. 2008, 3, 210-214
-
(2008)
Nat. Protoc.
, vol.3
, pp. 210-214
-
-
Pérez-Fuertes, Y.1
Kelly, A.M.2
Fossey, J.S.3
Powell, M.E.4
Bull, S.D.5
James, T.D.6
-
34
-
-
82455174223
-
Circular dichroism of multi-component assemblies for chiral amine recognition and rapid ee determination
-
Metola, P.; Anslyn, E. V.; James, T. D.; Bull, S. D. Circular dichroism of multi-component assemblies for chiral amine recognition and rapid ee determination Chem. Sci. 2012, 3, 156-161
-
(2012)
Chem. Sci.
, vol.3
, pp. 156-161
-
-
Metola, P.1
Anslyn, E.V.2
James, T.D.3
Bull, S.D.4
-
35
-
-
34249686052
-
Application of electronic circular dichroism in configurational and conformational analysis of organic compounds
-
Berova, N.; Di Bari, L.; Pescitelli, G. Application of electronic circular dichroism in configurational and conformational analysis of organic compounds Chem. Soc. Rev. 2007, 36, 914-931
-
(2007)
Chem. Soc. Rev.
, vol.36
, pp. 914-931
-
-
Berova, N.1
Di Bari, L.2
Pescitelli, G.3
-
36
-
-
0033598235
-
Absolute configurations of N, N -dialkyl α-amino acids and β-amino alcohols from exciton-coupled circular dichroism spectra of Cu(II) complexes
-
Zahn, S. S.; Canary, J. W. J. Absolute configurations of N, N -dialkyl α-amino acids and β-amino alcohols from exciton-coupled circular dichroism spectra of Cu(II) complexes Org. Lett. 1999, 1, 861-864
-
(1999)
Org. Lett.
, vol.1
, pp. 861-864
-
-
Zahn, S.S.1
Canary, J.W.J.2
-
37
-
-
0037255836
-
Derivatization, complexation, and absolute configurational assignment of chiral primary amines: Application of exciton-coupled circular dichroism
-
Zhang, J.; Holmes, A. E.; Sharma, A.; Brooks, N. R.; Rarig, R. S.; Zubieta, J.; Canary, J. W. Derivatization, complexation, and absolute configurational assignment of chiral primary amines: Application of exciton-coupled circular dichroism Chirality 2003, 15, 180-189
-
(2003)
Chirality
, vol.15
, pp. 180-189
-
-
Zhang, J.1
Holmes, A.E.2
Sharma, A.3
Brooks, N.R.4
Rarig, R.S.5
Zubieta, J.6
Canary, J.W.7
-
38
-
-
0034017370
-
Porphyrins and metalloporphyrins: Versatile circular dichroic reporter groups for structural studies
-
Huang, X. X.; Nakanishi, K. K.; Berova, N. N. Porphyrins and metalloporphyrins: Versatile circular dichroic reporter groups for structural studies Chirality 2000, 12, 237-255
-
(2000)
Chirality
, vol.12
, pp. 237-255
-
-
Huang, X.X.1
Nakanishi, K.K.2
Berova, N.N.3
-
39
-
-
21244490493
-
A cationic zinc porphyrin as a chiroptical probe for Z-DNA
-
Balaz, M.; De Napoli, M.; Holmes, A. E.; Mammana, A.; Nakanishi, K.; Berova, N.; Purrello, R. A cationic zinc porphyrin as a chiroptical probe for Z-DNA Angew. Chem., Int. Ed. 2005, 44, 4006-4009
-
(2005)
Angew. Chem., Int. Ed.
, vol.44
, pp. 4006-4009
-
-
Balaz, M.1
De Napoli, M.2
Holmes, A.E.3
Mammana, A.4
Nakanishi, K.5
Berova, N.6
Purrello, R.7
-
40
-
-
0001255839
-
Porphyrins: Powerful chromophores for structural studies by exciton-coupled circular dichroism
-
Matile, S.; Berova, N.; Nakanishi, K.; Novkova, S.; Philipova, I.; Blagoev, B. Porphyrins: Powerful chromophores for structural studies by exciton-coupled circular dichroism J. Am. Chem. Soc. 1995, 117, 7021-7022
-
(1995)
J. Am. Chem. Soc.
, vol.117
, pp. 7021-7022
-
-
Matile, S.1
Berova, N.2
Nakanishi, K.3
Novkova, S.4
Philipova, I.5
Blagoev, B.6
-
41
-
-
0000362651
-
Chirality-memory molecule: AD 2-symmetric fully substituted porphyrin as a conceptually new chirality sensor
-
Furusho, Y.; Kimura, T.; Mizuno, Y. Chirality-memory molecule: AD 2-symmetric fully substituted porphyrin as a conceptually new chirality sensor J. Am. Chem. Soc. 1997, 119, 5267-5268
-
(1997)
J. Am. Chem. Soc.
, vol.119
, pp. 5267-5268
-
-
Furusho, Y.1
Kimura, T.2
Mizuno, Y.3
-
42
-
-
68949122391
-
An unusual conformation of α-haloamides due to cooperative binding with zincated porphyrins
-
Tanasova, M.; Yang, Q.; Olmsted, C. C. An unusual conformation of α-haloamides due to cooperative binding with zincated porphyrins Eur. J. Org. Chem. 2009, 4242-4253
-
(2009)
Eur. J. Org. Chem.
, pp. 4242-4253
-
-
Tanasova, M.1
Yang, Q.2
Olmsted, C.C.3
-
43
-
-
0034837951
-
Supramolecular chirogenesis in zinc porphyrins: Mechanism, role of guest structure, and application for the absolute configuration determination
-
Borovkov, V. V.; Lintuluoto, J. M.; Inoue, Y. Supramolecular chirogenesis in zinc porphyrins: mechanism, role of guest structure, and application for the absolute configuration determination J. Am. Chem. Soc. 2001, 123, 2979-2989
-
(2001)
J. Am. Chem. Soc.
, vol.123
, pp. 2979-2989
-
-
Borovkov, V.V.1
Lintuluoto, J.M.2
Inoue, Y.3
-
44
-
-
57149103708
-
Prompt determination of absolute configuration for epoxy alcohols via exciton chirality protocol
-
Li, X.; Borhan, B. Prompt determination of absolute configuration for epoxy alcohols via exciton chirality protocol J. Am. Chem. Soc. 2008, 130, 16126-16127
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 16126-16127
-
-
Li, X.1
Borhan, B.2
-
45
-
-
84861898040
-
Absolute configuration for 1, n -glycols: A nonempirical approach to long-range stereochemical determination
-
Li, X.; Burrell, C. E.; Staples, R. J.; Borhan, B. Absolute configuration for 1, n -glycols: A nonempirical approach to long-range stereochemical determination J. Am. Chem. Soc. 2012, 134, 9026-9029
-
(2012)
J. Am. Chem. Soc.
, vol.134
, pp. 9026-9029
-
-
Li, X.1
Burrell, C.E.2
Staples, R.J.3
Borhan, B.4
-
46
-
-
46849085800
-
A chemical/computational approach to the determination of absolute configuration of flexible and transparent molecules: Aliphatic diols as a case study
-
Tartaglia, S.; Padula, D.; Scafato, P.; Chiummiento, L.; Rosini, C. A chemical/computational approach to the determination of absolute configuration of flexible and transparent molecules: Aliphatic diols as a case study J. Org. Chem. 2008, 73, 4865-4873
-
(2008)
J. Org. Chem.
, vol.73
, pp. 4865-4873
-
-
Tartaglia, S.1
Padula, D.2
Scafato, P.3
Chiummiento, L.4
Rosini, C.5
-
47
-
-
70450169432
-
Chiral amplification with a stereodynamic triaryl probe: Assignment of the absolute configuration and enantiomeric excess of amino alcohols
-
Ghosn, M. W.; Wolf, C. Chiral amplification with a stereodynamic triaryl probe: Assignment of the absolute configuration and enantiomeric excess of amino alcohols J. Am. Chem. Soc. 2009, 131, 16360-16361
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 16360-16361
-
-
Ghosn, M.W.1
Wolf, C.2
-
48
-
-
79956111867
-
Synthesis, conformational stability, and asymmetric transformation of atropisomeric 1,8-bisphenolnaphthalenes
-
Ghosn, M. W. M.; Wolf, C. C. Synthesis, conformational stability, and asymmetric transformation of atropisomeric 1,8-bisphenolnaphthalenes J. Org. Chem. 2011, 76, 3888-3897
-
(2011)
J. Org. Chem.
, vol.76
, pp. 3888-3897
-
-
Ghosn, M.W.M.1
Wolf, C.C.2
-
49
-
-
84866390169
-
Absolute stereochemical determination of chiral carboxylates using an achiral molecular tweezer
-
Yoon, H.; Lee, C.-H.; Jang, W.-D. Absolute stereochemical determination of chiral carboxylates using an achiral molecular tweezer Chem.-Eur. J. 2012, 18, 12479-12486
-
(2012)
Chem.-Eur. J.
, vol.18
, pp. 12479-12486
-
-
Yoon, H.1
Lee, C.-H.2
Jang, W.-D.3
-
50
-
-
84864669492
-
Induced circular dichroism in chiral N-methyl amides possessing an achiral binaphthyl chromophore and its application to absolute configuration determination of aliphatic chiral amines
-
Fujiwara, T.; Taniguchi, Y.; Katsumoto, Y.; Tanaka, T.; Node, M.; Ozeki, M.; Yamashita, M.; Hosoi, S. Induced circular dichroism in chiral N-methyl amides possessing an achiral binaphthyl chromophore and its application to absolute configuration determination of aliphatic chiral amines Tetrahedron: Asymmetry 2012, 23, 981-991
-
(2012)
Tetrahedron: Asymmetry
, vol.23
, pp. 981-991
-
-
Fujiwara, T.1
Taniguchi, Y.2
Katsumoto, Y.3
Tanaka, T.4
Node, M.5
Ozeki, M.6
Yamashita, M.7
Hosoi, S.8
-
51
-
-
79952273541
-
A stereodynamic probe providing a chiroptical response to substrate-controlled induction of an axially chiral arylacetylene framework
-
Iwaniuk, D. P.; Wolf, C. A stereodynamic probe providing a chiroptical response to substrate-controlled induction of an axially chiral arylacetylene framework J. Am. Chem. Soc. 2011, 133, 2414-2417
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 2414-2417
-
-
Iwaniuk, D.P.1
Wolf, C.2
-
52
-
-
78651387425
-
Effective chirogenesis in a bis(metallosalphen) complex through host-guest binding with carboxylic acids
-
Wezenberg, S. J.; Salassa, G.; Escudero-Adán, E. C.; Benet-Buchholz, J.; Kleij, A. W. Effective chirogenesis in a bis(metallosalphen) complex through host-guest binding with carboxylic acids Angew. Chem., Int. Ed. 2011, 50, 713-716
-
(2011)
Angew. Chem., Int. Ed.
, vol.50
, pp. 713-716
-
-
Wezenberg, S.J.1
Salassa, G.2
Escudero-Adán, E.C.3
Benet-Buchholz, J.4
Kleij, A.W.5
-
53
-
-
67249093403
-
Synthesis, conformation and chiroptical properties of diaryl esters of tartaric acid
-
Cysewski, R.; Kwit, M.; Warzajtis, B.; Rychlewska, U.; Gawroński, J. Synthesis, conformation and chiroptical properties of diaryl esters of tartaric acid J. Org. Chem. 2009, 74, 4573-4583
-
(2009)
J. Org. Chem.
, vol.74
, pp. 4573-4583
-
-
Cysewski, R.1
Kwit, M.2
Warzajtis, B.3
Rychlewska, U.4
Gawroński, J.5
-
54
-
-
55249090431
-
Highly stereospecific generation of helical chirality by imprinting with amino acids: A universal sensor for amino acid enantiopurity
-
Kim, H.; So, S. M.; Yen, C. P.-H.; Vinhato, E.; Lough, A. J.; Hong, J.-I.; Kim, H.-J.; Chin, J. Highly stereospecific generation of helical chirality by imprinting with amino acids: a universal sensor for amino acid enantiopurity Angew. Chem., Int. Ed. 2008, 47, 8657-8660
-
(2008)
Angew. Chem., Int. Ed.
, vol.47
, pp. 8657-8660
-
-
Kim, H.1
So, S.M.2
Yen, C.P.-H.3
Vinhato, E.4
Lough, A.J.5
Hong, J.-I.6
Kim, H.-J.7
Chin, J.8
-
55
-
-
77950163253
-
Probing molecular chirality by CD-sensitive dimeric metalloporphyrin hosts
-
Berova, N.; Pescitelli, G.; Petrovic, A. G.; Proni, G. Probing molecular chirality by CD-sensitive dimeric metalloporphyrin hosts Chem. Commun. 2009, 5958-5958
-
(2009)
Chem. Commun.
, pp. 5958-5958
-
-
Berova, N.1
Pescitelli, G.2
Petrovic, A.G.3
Proni, G.4
-
56
-
-
84892798883
-
Rapid determination of enantiomeric excess of α-chiral aldehydes using circular dichroism spectroscopy
-
Barman, S.; Anslyn, E. V. Rapid determination of enantiomeric excess of α-chiral aldehydes using circular dichroism spectroscopy Tetrahedron 2014, 70, 1357-1362
-
(2014)
Tetrahedron
, vol.70
, pp. 1357-1362
-
-
Barman, S.1
Anslyn, E.V.2
-
57
-
-
80052096646
-
A simple method for the determination of enantiomeric excess and identity of chiral carboxylic acids
-
Joyce, L. A.; Maynor, M. S.; Dragna, J. M.; da Cruz, G. M.; Lynch, V. M.; Canary, J. W.; Anslyn, E. V. A simple method for the determination of enantiomeric excess and identity of chiral carboxylic acids J. Am. Chem. Soc. 2011, 133, 13746-13752
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 13746-13752
-
-
Joyce, L.A.1
Maynor, M.S.2
Dragna, J.M.3
Da Cruz, G.M.4
Lynch, V.M.5
Canary, J.W.6
Anslyn, E.V.7
-
58
-
-
84862547512
-
Enantio- and chemoselective differentiation of protected α-amino acids and β-homoamino acids with a single copper(II) host
-
Joyce, L. A.; Canary, J. W.; Anslyn, E. V. Enantio- and chemoselective differentiation of protected α-amino acids and β-homoamino acids with a single copper(II) host Chem.-Eur. J. 2012, 18, 8064-8069
-
(2012)
Chem.-Eur. J.
, vol.18
, pp. 8064-8069
-
-
Joyce, L.A.1
Canary, J.W.2
Anslyn, E.V.3
-
59
-
-
82055208121
-
Dynamic multi-component covalent assembly for the reversible binding of secondary alcohols and chirality sensing
-
You, L.; Berman, J. S.; Anslyn, E. V. Dynamic multi-component covalent assembly for the reversible binding of secondary alcohols and chirality sensing Nat. Chem. 2011, 3, 943-948
-
(2011)
Nat. Chem.
, vol.3
, pp. 943-948
-
-
You, L.1
Berman, J.S.2
Anslyn, E.V.3
-
60
-
-
84860347312
-
An exciton-coupled circular dichroism protocol for the determination of identity, chirality, and enantiomeric excess of chiral secondary alcohols
-
You, L.; Pescitelli, G.; Anslyn, E. V.; Di Bari, L. An exciton-coupled circular dichroism protocol for the determination of identity, chirality, and enantiomeric excess of chiral secondary alcohols J. Am. Chem. Soc. 2012, 134, 7117-7125
-
(2012)
J. Am. Chem. Soc.
, vol.134
, pp. 7117-7125
-
-
You, L.1
Pescitelli, G.2
Anslyn, E.V.3
Di Bari, L.4
-
61
-
-
84860327193
-
Correlating sterics parameters and diastereomeric ratio values for a multicomponent assembly to predict exciton-coupled circular dichroism intensity and thereby enantiomeric excess of chiral secondary alcohols
-
You, L.; Berman, J. S.; Lucksanawichien, A.; Anslyn, E. V. Correlating sterics parameters and diastereomeric ratio values for a multicomponent assembly to predict exciton-coupled circular dichroism intensity and thereby enantiomeric excess of chiral secondary alcohols J. Am. Chem. Soc. 2012, 134, 7126-7134
-
(2012)
J. Am. Chem. Soc.
, vol.134
, pp. 7126-7134
-
-
You, L.1
Berman, J.S.2
Lucksanawichien, A.3
Anslyn, E.V.4
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