-
3
-
-
64149103140
-
Structure-function relationships in peptoids: Recent advances toward deciphering the structural requirements for biological function
-
Fowler, S. A. & Blackwell, H. E. Structure-function relationships in peptoids: recent advances toward deciphering the structural requirements for biological function. Org. Biomol. Chem. 7, 1508-1524 (2009)
-
(2009)
Org. Biomol. Chem
, vol.7
, pp. 1508-1524
-
-
Fowler, S.A.1
Blackwell, H.E.2
-
4
-
-
0028260073
-
DNA-like double helix formed by peptide nucleic acid
-
DOI 10.1038/368561a0
-
Wittung, P., Nielsen, P. E., Buchardt, O., Egholm, M. & Norden, B. DNA-like double helix formed by peptide nucleic acid. Nature 368, 561-563 (1994) (Pubitemid 24118775)
-
(1994)
Nature
, vol.368
, Issue.6471
, pp. 561-563
-
-
Wittung, P.1
Nielsen, P.E.2
Buchardt, O.3
Egholm, M.4
Norden, B.5
-
5
-
-
0034830898
-
Molecular recognition of DNA by small molecules
-
DOI 10.1016/S0968-0896(01)00262-0, PII S0968089601002620
-
Dervan, P. B. Molecular recognition of DNA by small molecules. Bioorgan. Med. Chem. 9, 2215-2235 (2001) (Pubitemid 32834613)
-
(2001)
Bioorganic and Medicinal Chemistry
, vol.9
, Issue.9
, pp. 2215-2235
-
-
Dervan, P.B.1
-
6
-
-
79960965295
-
-
ed. Goodchild, J. Ch. 1 Humana Press
-
Goodchild, J. in Therapeutic Oligonucleotides Vol. 764 (ed. Goodchild, J.) Ch. 1, 1-15 (Humana Press, 2011)
-
(2011)
Therapeutic Oligonucleotides
, vol.764
, pp. 1-15
-
-
Goodchild, J.1
-
7
-
-
41149084993
-
Conformational dynamics for chemical sensing: Simplicity and diversity
-
DOI 10.1039/b715673c
-
Riddle, J. A., Jiang, X. & Lee, D. Conformational dynamics for chemical sensing: simplicity and diversity. Analyst 133, 417-422 (2008) (Pubitemid 351441964)
-
(2008)
Analyst
, vol.133
, Issue.4
, pp. 417-422
-
-
Riddle, J.A.1
Jiang, X.2
Lee, D.3
-
8
-
-
0034658624
-
Molecular signal transduction through conformational transmission of a perhydroanthracene transducer
-
DOI 10.1002/(SICI)1521-3773(20000515)39:10<1835::AID-ANIE1835>3.0. CO;2-S
-
Krauss, R., Weinig, H-G., Seydack, M., Bendig, J. & Koert, U. Molecular signal transduction through conformational transmission of a perhydroanthracene transducer. Angew. Chem. Int. Ed. 39, 1835-1837 (2000) (Pubitemid 30365776)
-
(2000)
Angewandte Chemie - International Edition
, vol.39
, Issue.10
, pp. 1835-1837
-
-
Krauss, R.1
Weinig, H.-G.2
Seydack, M.3
Bendig, J.4
Koert, U.5
-
9
-
-
64349116529
-
Transfer of noncovalent chiral information along an optically inactive helical peptide chain: Allosteric control of asymmetry of the C-terminal site by external molecule that binds to the N-terminal site
-
Ousaka, N. & Inai, Y. Transfer of noncovalent chiral information along an optically inactive helical peptide chain: allosteric control of asymmetry of the C-terminal site by external molecule that binds to the N-terminal site. J. Org. Chem. 74, 1429-1439 (2009)
-
(2009)
J. Org. Chem
, vol.74
, pp. 1429-1439
-
-
Ousaka, N.1
Inai, Y.2
-
10
-
-
0035542909
-
A field guide to foldamers
-
Hill, D. J., Mio, M. J., Prince, R. B., Hughes, T. S. & Moore, J. S. A field guide to foldamers. Chem. Rev. 101, 3893-4012 (2001)
-
(2001)
Chem. Rev
, vol.101
, pp. 3893-4012
-
-
Hill, D.J.1
Mio, M.J.2
Prince, R.B.3
Hughes, T.S.4
Moore, J.S.5
-
12
-
-
73249140329
-
Helical polymers: Synthesis structures, and functions
-
Yashima, E., Maeda, K., Iida, H., Furusho, Y. & Nagai, K. Helical polymers: synthesis, structures, and functions. Chem. Rev. 109, 6102-6211 (2009)
-
(2009)
Chem. Rev
, vol.109
, pp. 6102-6211
-
-
Yashima, E.1
Maeda, K.2
Iida, H.3
Furusho, Y.4
Nagai, K.5
-
13
-
-
0035781183
-
Synthetic helical polymers: Conformation and function
-
DOI 10.1021/cr0000978
-
Nakano, T. & Okamoto, Y. Synthetic helical polymers: conformation and function. Chem. Rev. 101, 4013-4038 (2001) (Pubitemid 35373051)
-
(2001)
Chemical Reviews
, vol.101
, Issue.12
, pp. 4013-4038
-
-
Nakano, T.1
Okamoto, Y.2
-
14
-
-
33845184268
-
Macromolecular stereochemistry: The out-of-proportion influence of optically active comonomers on the conformational characteristics of polyisocyanates. The sergeants and soldiers experiment
-
Green, M. M. et al. Macromolecular stereochemistry: the out-of-proportion influence of optically active comonomers on the conformational characteristics of polyisocyanates. The sergeants and soldiers experiment. J. Am. Chem. Soc. 111, 6452-6454 (1989)
-
(1989)
J. Am. Chem. Soc
, vol.111
, pp. 6452-6454
-
-
Green, M.M.1
-
15
-
-
6744266061
-
A helical polymer with a cooperative response to chiral information
-
Green, M. M. et al. A helical polymer with a cooperative response to chiral information. Science 268, 1860-1866 (1995)
-
(1995)
Science
, vol.268
, pp. 1860-1866
-
-
Green, M.M.1
-
16
-
-
84923332640
-
Poly((4-carboxyphenyl)acetylene) as a probe for chirality assignment of amines by circular dichroism
-
Yashima, E., Matsushima, T. & Okamoto, Y. Poly((4-carboxyphenyl) acetylene) as a probe for chirality assignment of amines by circular dichroism. J. Am. Chem. Soc. 117, 11596-11597 (1995)
-
(1995)
J. Am. Chem. Soc
, vol.117
, pp. 11596-11597
-
-
Yashima, E.1
Matsushima, T.2
Okamoto, Y.3
-
17
-
-
0032507280
-
Trapped kinetic states, chiral amplification and molecular chaperoning in synthetic polymers: Chiral induction in polyguanidines through ion pair interactions [13]
-
DOI 10.1021/ja974048x
-
Schlitzer, D. S. & Novak, B. M. Trapped kinetic states, chiral amplification and molecular chaperoning in synthetic polymers: chiral induction in polyguanidines through ion pair interactions. J. Am. Chem. Soc. 120, 2196-2197 (1998) (Pubitemid 28179201)
-
(1998)
Journal of the American Chemical Society
, vol.120
, Issue.9
, pp. 2196-2197
-
-
Schlitzer, D.S.1
Novak, B.M.2
-
18
-
-
70349925664
-
Quantifying end-toend conformational communication of chirality through an achiral peptide chain
-
Clayden, J., Castellanos, A., Solà, J. & Morris, G. A. Quantifying end-toend conformational communication of chirality through an achiral peptide chain. Angew. Chem. Int. Ed. 48, 5962-5965 (2009)
-
(2009)
Angew. Chem. Int. Ed
, vol.48
, pp. 5962-5965
-
-
Clayden, J.1
Castellanos, A.2
Solà, J.3
Morris, G.A.4
-
19
-
-
25144474487
-
Chiral induction in quinoline-derived oligoamide foldamers: Assignment of helical handedness and role of steric effects
-
DOI 10.1021/ja0527828
-
Dolain, C., Jiang, H., Léger, J-M., Guionneau, P. & Huc, I. Chiral induction in quinoline-derived oligoamide foldamers: assignment of helical handedness and role of steric effects. J. Am. Chem. Soc. 127, 12943-12951 (2005) (Pubitemid 41339178)
-
(2005)
Journal of the American Chemical Society
, vol.127
, Issue.37
, pp. 12943-12951
-
-
Dolain, C.1
Jiang, H.2
Leger, J.-M.3
Guionneau, P.4
Huc, I.5
-
20
-
-
34250832094
-
Molecular transmission: Controlling the twist sense of a helical polymer with a single light-driven molecular motor
-
DOI 10.1002/anie.200604941
-
Pijper, D. & Feringa, B. L. Molecular transmission: controlling the twist sense of a helical polymer with a single light-driven molecular motor. Angew. Chem. Int. Ed. 46, 3693-3696 (2007) (Pubitemid 46981251)
-
(2007)
Angewandte Chemie - International Edition
, vol.46
, Issue.20
, pp. 3693-3696
-
-
Pijper, D.1
Feringa, B.L.2
-
21
-
-
80155155922
-
Chiral information harvesting in dendritic metallopeptides
-
Ousaka, N., Takeyama, Y., Iida, H. & Yashima, E. Chiral information harvesting in dendritic metallopeptides. Nature Chem. 3, 856-861 (2011)
-
(2011)
Nature Chem
, vol.3
, pp. 856-861
-
-
Ousaka, N.1
Takeyama, Y.2
Iida, H.3
Yashima, E.4
-
22
-
-
84875856640
-
Anion-driven reversible switching of metal-centered stereoisomers in metallopeptides
-
Ousaka, N., Takeyama, Y. & Yashima, E. Anion-driven reversible switching of metal-centered stereoisomers in metallopeptides. Chem. Eur. J. 19, 4680-4685 (2013)
-
(2013)
Chem. Eur. J
, vol.19
, pp. 4680-4685
-
-
Ousaka, N.1
Takeyama, Y.2
Yashima, E.3
-
23
-
-
77956589648
-
Nanometer-range communication of stereochemical information by reversible switching of molecular helicity
-
Solà, J., Fletcher, S. P., Castellanos, A. & Clayden, J. Nanometer-range communication of stereochemical information by reversible switching of molecular helicity. Angew. Chem. Int. Ed. 49, 6836-6839 (2010)
-
(2010)
Angew. Chem. Int. Ed
, vol.49
, pp. 6836-6839
-
-
Solà, J.1
Fletcher, S.P.2
Castellanos, A.3
Clayden, J.4
-
24
-
-
84867317117
-
Coordination chemistry strategies for dynamic helicates: Time-programmable chirality switching with labile and inert metal helicates
-
Miyake, H. & Tsukube, H. Coordination chemistry strategies for dynamic helicates: time-programmable chirality switching with labile and inert metal helicates. Chem. Soc. Rev. 41, 6977-6991 (2012)
-
(2012)
Chem. Soc. Rev
, vol.41
, pp. 6977-6991
-
-
Miyake, H.1
Tsukube, H.2
-
25
-
-
84866241652
-
Transfer of chirality from ligands to metal centers: Recent examples
-
Crassous, J. Transfer of chirality from ligands to metal centers: recent examples. Chem. Commun. 48, 9687-9695 (2012)
-
(2012)
Chem. Commun
, vol.48
, pp. 9687-9695
-
-
Crassous, J.1
-
26
-
-
84867355275
-
Aromatic amide foldamers: Structures, properties, and functions
-
Zhang, D-W., Zhao, X., Hou, J-L. & Li, Z-T. Aromatic amide foldamers: structures, properties, and functions. Chem. Rev. 112, 5271-5316 (2012)
-
(2012)
Chem. Rev
, vol.112
, pp. 5271-5316
-
-
Zhang, D.-W.1
Zhao, X.2
Hou, J.-L.3
Li, Z.-T.4
-
27
-
-
38349110900
-
Timeprogrammed peptide helix inversion of a synthetic metal complex triggered by an achiral NO3 2 anion
-
Miyake, H., Kamon, H., Miyahara, I., Sugimoto, H. & Tsukube, H. Timeprogrammed peptide helix inversion of a synthetic metal complex triggered by an achiral NO3 2 anion. J. Am. Chem. Soc. 130, 792-793 (2007)
-
(2007)
J. Am. Chem. Soc
, vol.130
, pp. 792-793
-
-
Miyake, H.1
Kamon, H.2
Miyahara, I.3
Sugimoto, H.4
Tsukube, H.5
-
28
-
-
61349093028
-
Transmission of stereochemical information over nanometre distances in chemical reactions
-
Clayden, J. Transmission of stereochemical information over nanometre distances in chemical reactions. Chem. Soc. Rev. 38, 817-829 (2009)
-
(2009)
Chem. Soc. Rev
, vol.38
, pp. 817-829
-
-
Clayden, J.1
-
29
-
-
0029272840
-
Chiral discrimination of monosaccharides using a fluorescent molecular sensor
-
James, T. D., Samankumara Sandanayake, K. R. A. & Shinkai, S. Chiral discrimination of monosaccharides using a fluorescent molecular sensor. Nature 374, 345-347 (1995)
-
(1995)
Nature
, vol.374
, pp. 345-347
-
-
James, T.D.1
Samankumara Sandanayake, K.R.A.2
Shinkai, S.3
-
31
-
-
33645467008
-
An improved class of sugar-binding boronic acids, soluble and capable of complexing glycosides in neutral water
-
Dowlut, M. & Hall, D. G. An improved class of sugar-binding boronic acids, soluble and capable of complexing glycosides in neutral water. J. Am. Chem. Soc. 128, 4226-4227 (2006)
-
(2006)
J. Am. Chem. Soc
, vol.128
, pp. 4226-4227
-
-
Dowlut, M.1
Hall, D.G.2
-
32
-
-
0035471131
-
Design of folded peptides
-
DOI 10.1021/cr000053z
-
Venkatraman, J., Shankaramma, S. C. & Balaram, P. Design of folded peptides. Chem. Rev. 101, 3131-3152 (2001) (Pubitemid 35377814)
-
(2001)
Chemical Reviews
, vol.101
, Issue.10
, pp. 3131-3152
-
-
Venkatraman, J.1
Shankaramma, S.C.2
Balaram, P.3
-
34
-
-
84985628243
-
Conformational transitions between enantiomeric 310-helices
-
Hummel, R-P., Toniolo, C. & Jung, G. Conformational transitions between enantiomeric 310-helices. Angew. Chem. Int. Ed. 26, 1150-1152 (1987)
-
(1987)
Angew. Chem. Int. Ed
, vol.26
, pp. 1150-1152
-
-
Hummel, R.-P.1
Toniolo, C.2
Jung, G.3
-
35
-
-
79952751114
-
Measuring screw-sense preference in a helical oligomer by comparison of 13C NMR signal separation at slow and fast exchange
-
Solà, J., Morris, G. A. & Clayden, J. Measuring screw-sense preference in a helical oligomer by comparison of 13C NMR signal separation at slow and fast exchange. J. Am. Chem. Soc. 133, 3712-3715 (2011)
-
(2011)
J. Am. Chem. Soc
, vol.133
, pp. 3712-3715
-
-
Solà, J.1
Morris, G.A.2
Clayden, J.3
-
36
-
-
84857837907
-
Chemical communication: Conductors and insulators of screw-sense preference between helical oligo(aminoisobutyric acid) domains
-
Boddaert, T., Sola, J., Helliwell, M. & Clayden, J. Chemical communication: conductors and insulators of screw-sense preference between helical oligo(aminoisobutyric acid) domains. Chem. Commun. 48, 3397-3399 (2012)
-
(2012)
Chem. Commun
, vol.48
, pp. 3397-3399
-
-
Boddaert, T.1
Sola, J.2
Helliwell, M.3
Clayden, J.4
-
37
-
-
80052982792
-
Synthesis of enantiomerically enriched (R)-13C-labelled 2-aminoisobutyric acid (Aib) by conformational memory in the alkylation of a derivative of L-alanine
-
Fletcher, S. P., Solà, J., Holt, D., Brown, R. A. & Clayden, J. Synthesis of enantiomerically enriched (R)-13C-labelled 2-aminoisobutyric acid (Aib) by conformational memory in the alkylation of a derivative of L-alanine. Beilstein J. Org. Chem. 7, 1304-1309 (2011)
-
(2011)
Beilstein J. Org. Chem
, vol.7
, pp. 1304-1309
-
-
Fletcher, S.P.1
Solà, J.2
Holt, D.3
Brown, R.A.4
Clayden, J.5
-
38
-
-
0035799849
-
a values and geometries of secondary and tertiary amines complexed to boronic acids - Implications for sensor design
-
DOI 10.1021/ol0156805
-
Wiskur, S. L. et al. pKa Values and geometries of secondary and tertiary amines complexed to boronic acids-implications for sensor design. Org. Lett. 3, 1311-1314 (2001) (Pubitemid 33629453)
-
(2001)
Organic Letters
, vol.3
, Issue.9
, pp. 1311-1314
-
-
Wiskur, S.L.1
Lavigne, J.J.2
Ait-Haddou, H.3
Lynch, V.4
Chiu, Y.H.5
Canary, J.W.6
Anslyn, E.V.7
-
39
-
-
34248377816
-
-
ed. Schrader, T. Ch. 110 Springer
-
James, T. in Creative Chemical Sensor Systems Vol. 277 (ed. Schrader, T.) Ch. 110, 107-152 (Springer, 2007)
-
(2007)
Creative Chemical Sensor Systems
, vol.277
, pp. 107-152
-
-
James, T.1
-
40
-
-
31944449355
-
A structural investigation of the N-B interaction in an o-(N,N-dialkylaminomethyl)arylboronate system
-
DOI 10.1021/ja055817c
-
Zhu, L. et al. A structural investigation of the N-B interaction in an o-(N,N-dialkylaminomethyl)arylboronate system. J. Am. Chem. Soc. 128, 1222-1232 (2006) (Pubitemid 43190634)
-
(2006)
Journal of the American Chemical Society
, vol.128
, Issue.4
, pp. 1222-1232
-
-
Zhu, L.1
Shabbir, S.H.2
Gray, M.3
Lynch, V.M.4
Sorey, S.5
Anslyn, E.V.6
-
41
-
-
66249103333
-
Probing intramolecular B-N interactions in orthoaminomethyl arylboronic acids
-
Collins, B. E. et al. Probing intramolecular B-N interactions in orthoaminomethyl arylboronic acids. J. Org. Chem. 74, 4055-4060 (2009)
-
(2009)
J. Org. Chem
, vol.74
, pp. 4055-4060
-
-
Collins, B.E.1
-
42
-
-
84873305305
-
On the rate of boronate ester formation in ortho-aminomethyl- functionalised phenyl boronic acids
-
Collins, B. E., Metola, P. & Anslyn, E. V. On the rate of boronate ester formation in ortho-aminomethyl-functionalised phenyl boronic acids. Supramol. Chem. 25, 79-86 (2012)
-
(2012)
Supramol. Chem.
, vol.25
, pp. 79-86
-
-
Collins, B.E.1
Metola, P.2
Anslyn, E.V.3
-
43
-
-
0042074618
-
10-helix equilibrium: A heptapeptide behaves as a solvent-driven molecular spring
-
DOI 10.1002/anie.200351015
-
Pengo, P. et al. Quantitative correlation of solvent polarity with the a-/310-helix equilibrium: a heptapeptide behaves as a solvent-driven molecular spring. Angew. Chem. Int. Ed. 42, 3388-3392 (2003) (Pubitemid 36980575)
-
(2003)
Angewandte Chemie - International Edition
, vol.42
, Issue.29
, pp. 3388-3392
-
-
Pengo, P.1
Pasquato, L.2
Moro, S.3
Brigo, A.4
Fogolari, F.5
Broxterman, Q.B.6
Kaptein, B.7
Scrimin, P.8
-
44
-
-
34548499896
-
A comparative study of the relative stability of representative chiral and achiral boronic esters employing transesterification
-
Roy, C. D. & Brown, H. C. A comparative study of the relative stability of representative chiral and achiral boronic esters employing transesterification. Monatsh. Chem. 138, 879-887 (2007)
-
(2007)
Monatsh. Chem
, vol.138
, pp. 879-887
-
-
Roy, C.D.1
Brown, H.C.2
-
45
-
-
84863012106
-
Induction of unexpected left-handed helicity by an N-terminal L-amino acid in an otherwise achiral peptide chain
-
Brown, R. A., Marcelli, T., De Poli, M., Solà, J. & Clayden, J. Induction of unexpected left-handed helicity by an N-terminal L-amino acid in an otherwise achiral peptide chain. Angew. Chem. Int. Ed. 51, 1395-1399 (2012)
-
(2012)
Angew. Chem. Int. Ed
, vol.51
, pp. 1395-1399
-
-
Brown, R.A.1
Marcelli, T.2
De Poli, M.3
Solà, J.4
Clayden, J.5
-
46
-
-
0021104058
-
Lipid bilayer thickness varies linearly with acyl chain length in fluid phosphatidylcholine vesicles
-
Lewis, B. A. & Engelman, D. M. Lipid bilayer thickness varies linearly with acyl chain length in fluid phosphatidylcholine vesicles. J. Mol. Biol. 166, 211-217 (1983)
-
(1983)
J. Mol. Biol
, vol.166
, pp. 211-217
-
-
Lewis, B.A.1
Engelman, D.M.2
-
47
-
-
79954782236
-
Structure of an agonist-bound human A2A adenosine receptor
-
Xu, F. et al. Structure of an agonist-bound human A2A adenosine receptor. Science 332, 322-327 (2011)
-
(2011)
Science
, vol.332
, pp. 322-327
-
-
Xu, F.1
-
48
-
-
77955984298
-
The crystallographic structure of the human adenosine A2A receptor in a high-affinity antagonist-bound state: Implications for GPCR drug screening and design
-
Jaakola, V-P. & Ijzerman, A. P. The crystallographic structure of the human adenosine A2A receptor in a high-affinity antagonist-bound state: implications for GPCR drug screening and design. Curr. Opin. Struct. Biol. 20, 401-414 (2010)
-
(2010)
Curr. Opin. Struct. Biol
, vol.20
, pp. 401-414
-
-
Jaakola, V.-P.1
Ijzerman, A.P.2
-
49
-
-
0000568490
-
Molecular design of boronic acid-based dye receptors for nucleosides
-
Takeuchi, M., Taguchi, M., Shinmori, H. & Shinkai, S. Molecular design of boronic acid-based dye receptors for nucleosides. Bull. Chem. Soc. Jpn 69, 2613-2618 (1996) (Pubitemid 126476799)
-
(1996)
Bulletin of the Chemical Society of Japan
, vol.69
, Issue.9
, pp. 2613-2618
-
-
Takeuchi, M.1
Taguchi, M.2
Shinmori, H.3
Shinkai, S.4
-
50
-
-
0034860754
-
Organization of nucleosides supported by boronic-acid-appended poly(L-lysine): Creation of a novel RNA mimic
-
DOI 10.1246/bcsj.74.1311
-
Kobayashi, H., Amaike, M., Koumoto, K. & Shinkai, S. Organization of nucleosides supported by boronic-acid-appended poly(L-lysine): creation of a novel RNA mimic. Bull. Chem. Soc. Jpn 74, 1311-1317 (2001) (Pubitemid 32786332)
-
(2001)
Bulletin of the Chemical Society of Japan
, vol.74
, Issue.7
, pp. 1311-1317
-
-
Kobayashi, H.1
Amaike, M.2
Koumoto, K.3
Shinkai, S.4
-
51
-
-
33748757941
-
Stereochemical and regiochemical trends in the selective detection of saccharides
-
DOI 10.1021/ja063651p
-
Jiang, S. et al. Stereochemical and regiochemical trends in the selective detection of saccharides. J. Am. Chem. Soc. 128, 12221-12228 (2006) (Pubitemid 44413853)
-
(2006)
Journal of the American Chemical Society
, vol.128
, Issue.37
, pp. 12221-12228
-
-
Jiang, S.1
Escobedo, J.O.2
Kim, K.K.3
Alpturk, O.4
Samoei, G.K.5
Fakayode, S.O.6
Warner, I.M.7
Rusin, O.8
Strongin, R.M.9
-
52
-
-
56949099992
-
Remarkably selective saccharide recognition by solid-supported peptide boronic acids
-
Duggan, P. J. & Offermann, D. A. Remarkably selective saccharide recognition by solid-supported peptide boronic acids. Tetrahedron 65, 109-114 (2009)
-
(2009)
Tetrahedron
, vol.65
, pp. 109-114
-
-
Duggan, P.J.1
Offermann, D.A.2
-
53
-
-
0026213245
-
O-Acetamidophenylboronate esters stabilized toward hydrolysis by an intramolecular O-B interaction: Potential linkers for selective bioconjugation via vicinal diol moieties of carbohydrates
-
Cai, S. X. & Keana, J. F. W. o-Acetamidophenylboronate esters stabilized toward hydrolysis by an intramolecular O-B interaction: potential linkers for selective bioconjugation via vicinal diol moieties of carbohydrates. Bioconj. Chem. 2, 317-322 (1991)
-
(1991)
Bioconj. Chem
, vol.2
, pp. 317-322
-
-
Cai, S.X.1
Keana, J.F.W.2
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