-
1
-
-
77956517003
-
-
Gutsche C D. Calixarenes revisited. In: Stoddart J F, ed. Monographs in Supramolecular Chemistry. London: Royal Society of Chemistry, 1998.
-
-
-
-
2
-
-
0004287470
-
-
Z. Asfari, V. Böhmer, and J. Harrowfield et al.(Eds.), Dordrecht, the Netherlands: Kluwer Academic Publishers
-
Asfari Z, Böhmer V, Harrowfield J, et al. eds. Calixarenes 2001. Dordrecht, the Netherlands: Kluwer Academic Publishers, 2001.
-
(2001)
Calixarenes 2001
-
-
-
3
-
-
0029785123
-
Colorimetric chiral recognition by a molecular sensor
-
Kubo Y, Maeda S, Tokita S, et al. Colorimetric chiral recognition by a molecular sensor. Nature, 1996, 382: 522-524.
-
(1996)
Nature
, vol.382
, pp. 522-524
-
-
Kubo, Y.1
Maeda, S.2
Tokita, S.3
-
4
-
-
0001648635
-
Synthesis of upper and lower rim binaphthyl bridged calix[4]arenes: New potential chiral hosts for molecular recognition and catalysis
-
Pinkhassik E, Stibor I, Casnati A, et al. Synthesis of upper and lower rim binaphthyl bridged calix[4]arenes: New potential chiral hosts for molecular recognition and catalysis. J Org Chem, 1997, 62: 8654-8659.
-
(1997)
J Org Chem
, vol.62
, pp. 8654-8659
-
-
Pinkhassik, E.1
Stibor, I.2
Casnati, A.3
-
5
-
-
0033537031
-
Transfer of chiral information through molecular assembly
-
Castellano R K, Nuckolls C, Rebek J Jr. Transfer of chiral information through molecular assembly. J Am Chem Soc, 1999, 121: 11156-11163.
-
(1999)
J Am Chem Soc
, vol.121
, pp. 11156-11163
-
-
Castellano, R.K.1
Nuckolls, C.2
Rebek Jr., J.3
-
6
-
-
2542499609
-
Exceptional chiral recognition of racemic carboxylic acids by calix[4]arenes bearing optically pure alpha,ss-amino alcohol groups
-
Zheng Y S, Zhang C. Exceptional chiral recognition of racemic carboxylic acids by calix[4]arenes bearing optically pure alpha, ss-amino alcohol groups. Org Lett, 2004, 6: 1189-1192.
-
(2004)
Org Lett
, vol.6
, pp. 1189-1192
-
-
Zheng, Y.S.1
Zhang, C.2
-
7
-
-
33644784660
-
Calix[4]arene alpha-aminophosphonic acids: Asymmetric synthesis and enantioselective inhibition of an alkaline phosphatase
-
Cherenok S, Vovk A, Muravyova I, et al. Calix[4]arene alpha-aminophosphonic acids: Asymmetric synthesis and enantioselective inhibition of an alkaline phosphatase. Org Lett, 2006, 8: 549-552.
-
(2006)
Org Lett
, vol.8
, pp. 549-552
-
-
Cherenok, S.1
Vovk, A.2
Muravyova, I.3
-
8
-
-
0034685439
-
Control of structural isomerism in noncovalent hydrogen-bonded assemblies using peripheral chiral information
-
Prins L J, Jolliffe K A, Hulst R, et al. Control of structural isomerism in noncovalent hydrogen-bonded assemblies using peripheral chiral information. J Am Chem Soc, 2000, 122: 3617-3627.
-
(2000)
J Am Chem Soc
, vol.122
, pp. 3617-3627
-
-
Prins, L.J.1
Jolliffe, K.A.2
Hulst, R.3
-
9
-
-
0000683605
-
Calixarenes 8. Short, stepwise synthesis of p-phenylcalix[4]arene, p-phenyl-p-tert-butylcalix[4]arene, and derived products
-
No K H, Gutsche C D. Calixarenes 8. Short, stepwise synthesis of p-phenylcalix[4]arene, p-phenyl-p-tert-butylcalix[4]arene, and derived products. J Org Chem, 1982, 47: 2713-2719.
-
(1982)
J Org Chem
, vol.47
, pp. 2713-2719
-
-
No, K.H.1
Gutsche, C.D.2
-
10
-
-
0033597259
-
Inherently chiral alpha-picolyloxy-p-tert-butyl-calix[5]arene crown ethers: Synthesis, structure proof, and enantioselective HPLC resolution
-
Caccamese S, Notti A, Pappalardo S, et al. Inherently chiral alpha-picolyloxy-p-tert-butyl-calix[5]arene crown ethers: Synthesis, structure proof, and enantioselective HPLC resolution. Tetrahedron, 1999, 55: 5505-5514.
-
(1999)
Tetrahedron
, vol.55
, pp. 5505-5514
-
-
Caccamese, S.1
Notti, A.2
Pappalardo, S.3
-
11
-
-
0034637271
-
Resolution of inherently chiral calix[4]arenes with AABB and CDCD substitution patterns on the upper and lower rims, respectively
-
Caccamese S, Bottino A, Cunsolo F, et al. Resolution of inherently chiral calix[4]arenes with AABB and CDCD substitution patterns on the upper and lower rims, respectively. Tetrahedron: Asymmetry, 2000, 11: 3103-3112.
-
(2000)
Tetrahedron: Asymmetry
, vol.11
, pp. 3103-3112
-
-
Caccamese, S.1
Bottino, A.2
Cunsolo, F.3
-
12
-
-
0012017025
-
Acid-promoted rearrangement of carbonate functionality anchored to the lower rim of a calix [4] arene skeleton: A new class of chiral calix[4]arene and its chiroptical properties
-
Hesek D, Inoue Y, Drew M G B, et al. Acid-promoted rearrangement of carbonate functionality anchored to the lower rim of a calix [4] arene skeleton: A new class of chiral calix[4]arene and its chiroptical properties. Org Lett, 2000, 2: 2237-2240.
-
(2000)
Org Lett
, vol.2
, pp. 2237-2240
-
-
Hesek, D.1
Inoue, Y.2
Drew, M.G.B.3
-
13
-
-
64149111012
-
Synthesis and resolution of a multifunctional inherently chiral calyx [4] arene with an ABCD substi- tution pattern at the wide rim: The effect of a multifunctional structure in the organocatalyst on enantioselectivity in asymmetric reactions
-
Shirakawa S, Kimura T, Murata S, et al. Synthesis and resolution of a multifunctional inherently chiral calyx [4] arene with an ABCD substi- tution pattern at the wide rim: The effect of a multifunctional structure in the organocatalyst on enantioselectivity in asymmetric reactions. J Org Chem, 2009, 74: 1288-1296.
-
(2009)
J Org Chem
, vol.74
, pp. 1288-1296
-
-
Shirakawa, S.1
Kimura, T.2
Murata, S.3
-
14
-
-
0346100542
-
Preparation of both antipodes of enantiopure inherently chiral calix[4]crowns
-
Cao Y D, Luo J, Zheng Q Y, et al. Preparation of both antipodes of enantiopure inherently chiral calix[4]crowns. J Org Chem, 2004, 69: 206-208.
-
(2004)
J Org Chem
, vol.69
, pp. 206-208
-
-
Cao, Y.D.1
Luo, J.2
Zheng, Q.Y.3
-
15
-
-
26844440038
-
Synthesis and optical resolution of a series of inherently chiral calix[4]crowns with cone and partial cone conformations
-
Luo J, Zheng Q Y, Chen C F, et al. Synthesis and optical resolution of a series of inherently chiral calix[4]crowns with cone and partial cone conformations. Chem Eur J, 2005, 11: 5917-5928.
-
(2005)
Chem Eur J
, vol.11
, pp. 5917-5928
-
-
Luo, J.1
Zheng, Q.Y.2
Chen, C.F.3
-
16
-
-
24944484200
-
Efficient syntheses and resolutions of inherently chiral calix[4]quinolines in the cone and partial-cone conformation
-
Mao R, Zheng Q Y, Chen C F, et al. Efficient syntheses and resolutions of inherently chiral calix[4]quinolines in the cone and partial-cone conformation. J Org Chem, 2005, 70: 7662-7671.
-
(2005)
J Org Chem
, vol.70
, pp. 7662-7671
-
-
Mao, R.1
Zheng, Q.Y.2
Chen, C.F.3
-
17
-
-
23044472599
-
Facile synthesis and optical resolution of inherently chiral fluorescent calix[4]crowns: Enantioselective recognition towards chiral leucinol
-
Luo J, Zheng Q Y, Chen C F, et al. Facile synthesis and optical resolution of inherently chiral fluorescent calix[4]crowns: Enantioselective recognition towards chiral leucinol. Tetrahedron, 2005, 61: 8517-8528.
-
(2005)
Tetrahedron
, vol.61
, pp. 8517-8528
-
-
Luo, J.1
Zheng, Q.Y.2
Chen, C.F.3
-
18
-
-
13844256417
-
Preparation of enantiopure inherently chiral calix[5]arenes
-
Li S Y, Zheng Q Y, Chen C F, et al. Preparation of enantiopure inherently chiral calix[5]arenes. Tetrahedron: Asymmetry, 2005, 16: 641-645.
-
(2005)
Tetrahedron: Asymmetry
, vol.16
, pp. 641-645
-
-
Li, S.Y.1
Zheng, Q.Y.2
Chen, C.F.3
-
19
-
-
0038162422
-
Synthesis and optical resolution of an anti-O,O′-dialkylated calix[4]arene
-
Narumi F, Yamabuki W, Hattori T, et al. Synthesis and optical resolution of an anti-O, O′-dialkylated calix[4]arene. Chem Lett, 2003, 32: 320-321.
-
(2003)
Chem Lett
, vol.32
, pp. 320-321
-
-
Narumi, F.1
Yamabuki, W.2
Hattori, T.3
-
20
-
-
13844254277
-
-
Tetrahedron: Asymmetry
-
Narumi F, Hattori T, Yamabuki W, et al. Resolution of inherently chiral anti-O, O′-dialkylated calix[4]arenes and determination of their absolute stereochemistries by CD and X-ray methods. Tetrahedron: Asymmetry, 2005, 16: 793-800.
-
(2005)
Resolution of Inherently Chiral Anti-O, O′-Dialkylated Calix[4]Arenes and Determination of Their Absolute Stereochemistries by CD and X-Ray Methods
, pp. 793-800
-
-
Narumi, F.1
Hattori, T.2
Yamabuki, W.3
-
21
-
-
4043095602
-
Synthesis of an inherently chiral O, O′-bridged thiacalix[4]crowncarboxylic acid and its application to a chiral solvating agent
-
Narumi F, Hattori T, Matsumura N, et al. Synthesis of an inherently chiral O, O′-bridged thiacalix[4]crowncarboxylic acid and its application to a chiral solvating agent. Tetrahedron, 2004, 60: 7827-7833.
-
(2004)
Tetrahedron
, vol.60
, pp. 7827-7833
-
-
Narumi, F.1
Hattori, T.2
Matsumura, N.3
-
22
-
-
33748967953
-
A stereoselective synthesis of asymmetrically substituted calyx [4] arene-carbamates
-
Boyko V I, Shivanyuk A, Pyrozhenko V V, et al. A stereoselective synthesis of asymmetrically substituted calyx [4] arene-carbamates. Tetrahedron Lett, 2006, 47: 7775-7778.
-
(2006)
Tetrahedron Lett
, vol.47
, pp. 7775-7778
-
-
Boyko, V.I.1
Shivanyuk, A.2
Pyrozhenko, V.V.3
-
23
-
-
34147155244
-
Diastereoselective lower rim (1S)-camphorsulfonylation as the shortest way to the inherently chiral calix[4]arene
-
Yakovenko A V, Boyko V I, Danylyuk O, et al. Diastereoselective lower rim (1S)-camphorsulfonylation as the shortest way to the inherently chiral calix[4]arene. Org Lett, 2007, 9: 1183-1185.
-
(2007)
Org Lett
, vol.9
, pp. 1183-1185
-
-
Yakovenko, A.V.1
Boyko, V.I.2
Danylyuk, O.3
-
24
-
-
34547942528
-
Design of a novel inherently chiral calix[4]arene for chiral molecular recognition
-
Shirakawa S, Moriyama A, Shimizu S. Design of a novel inherently chiral calix[4]arene for chiral molecular recognition. Org Lett, 2007, 9: 3117-3119.
-
(2007)
Org Lett
, vol.9
, pp. 3117-3119
-
-
Shirakawa, S.1
Moriyama, A.2
Shimizu, S.3
-
25
-
-
64149111012
-
Synthesis and resolution of a multifunctional inherently chiral calix[4]arene with an ABCD substitution pattern at the wide rim: The effect of a multifunctional structure in the organocatalyst on enantioselectivity in asymmetric reactions
-
Shirakawa S, Kimura T, Murata S, et al. Synthesis and resolution of a multifunctional inherently chiral calix[4]arene with an ABCD substitution pattern at the wide rim: The effect of a multifunctional structure in the organocatalyst on enantioselectivity in asymmetric reactions. J Org Chem, 2009, 74: 1288-1296.
-
(2009)
J Org Chem
, vol.74
, pp. 1288-1296
-
-
Shirakawa, S.1
Kimura, T.2
Murata, S.3
-
26
-
-
35948998795
-
A new approach to enantiopure inherently chiral calix[4]arenes: Determination of their absolute configurations
-
Xu Z X, Zhang C, Zheng Q Y, et al. A new approach to enantiopure inherently chiral calix[4]arenes: Determination of their absolute configurations. Org Lett, 2007, 9: 4447-4450.
-
(2007)
Org Lett
, vol.9
, pp. 4447-4450
-
-
Xu, Z.X.1
Zhang, C.2
Zheng, Q.Y.3
-
27
-
-
38949134778
-
Effective nonenzymatic kinetic resolution of racemic m-nitro-substituted inherently chiral aminocalix [4] arenes
-
Xu Z X, Zhang C, Yang Y, et al. Effective nonenzymatic kinetic resolution of racemic m-nitro-substituted inherently chiral aminocalix [4] arenes. Org Lett, 2008, 10: 477-479.
-
(2008)
Org Lett
, vol.10
, pp. 477-479
-
-
Xu, Z.X.1
Zhang, C.2
Yang, Y.3
-
28
-
-
10044228495
-
Synthesis and characterization of two new p-tert-butylcalix[4]arene Schiff bases
-
Alemi A A, Shaabani B, Dilmaghani K A, et al. Synthesis and characterization of two new p-tert-butylcalix[4]arene Schiff bases. Molecules, 2001, 6: 417-423.
-
(2001)
Molecules
, vol.6
, pp. 417-423
-
-
Alemi, A.A.1
Shaabani, B.2
Dilmaghani, K.A.3
-
29
-
-
0028924920
-
A novel approach to inherently chiral calix[4]arenes by direct introduction of a substitutent at the meta position
-
Verboom W, Bodewes P J, Essen G V, et al. A novel approach to inherently chiral calix[4]arenes by direct introduction of a substitutent at the meta position. Tetrahedron, 1995, 51: 499-512.
-
(1995)
Tetrahedron
, vol.51
, pp. 499-512
-
-
Verboom, W.1
Bodewes, P.J.2
Essen, G.V.3
-
30
-
-
33745043243
-
Highly selective C-H functionalization /halogenation of acetanilide
-
Wan X B, Ma Z X, Li B J, et al. Highly selective C-H functionalization /halogenation of acetanilide. J Am Chem Soc, 2006, 128: 7416-7417.
-
(2006)
J Am Chem Soc
, vol.128
, pp. 7416-7417
-
-
Wan, X.B.1
Ma, Z.X.2
Li, B.J.3
-
31
-
-
48049109173
-
Inherently chiral calix[4]arene based bifunctional organocatalysts for enantioselective aldol reactions
-
Xu Z X, Li G K, Chen C F, et al. Inherently chiral calix[4]arene based bifunctional organocatalysts for enantioselective aldol reactions. Tetrahedron, 2008, 64: 8668-8675.
-
(2008)
Tetrahedron
, vol.64
, pp. 8668-8675
-
-
Xu, Z.X.1
Li, G.K.2
Chen, C.F.3
-
32
-
-
0010911259
-
Synthesis and alkali-metal binding-properties of upper rim functionalized calix[4]arenes
-
Conner M, Janout V, Regen S L. Synthesis and alkali-metal binding-properties of upper rim functionalized calix[4]arenes. J Org Chem, 1992, 57: 3744-3746.
-
(1992)
J Org Chem
, vol.57
, pp. 3744-3746
-
-
Conner, M.1
Janout, V.2
Regen, S.L.3
-
33
-
-
0032509491
-
Synthesis of calix[4] arenylvinylene and calix[4]arenylphenylene oligomers by Stille and Suzuki cross-coupling reactions
-
Dondoni A, Ghiglione C, Marra A, et al. Synthesis of calix[4] arenylvinylene and calix[4]arenylphenylene oligomers by Stille and Suzuki cross-coupling reactions. J Org Chem, 1998, 63: 9535-9539.
-
(1998)
J Org Chem
, vol.63
, pp. 9535-9539
-
-
Dondoni, A.1
Ghiglione, C.2
Marra, A.3
|