-
1
-
-
11744250899
-
Asymmetric photochemistry in solution
-
H. Rau Asymmetric photochemistry in solution Chem. Rev. 1983 83 535 547
-
(1983)
Chem. Rev.
, vol.83
, pp. 535-547
-
-
Rau, H.1
-
2
-
-
0001013736
-
Asymmetric photochemical reactions in solution
-
Y. Inoue Asymmetric photochemical reactions in solution Chem. Rev. 1992 92 741 770
-
(1992)
Chem. Rev.
, vol.92
, pp. 741-770
-
-
Inoue, Y.1
-
3
-
-
85050326151
-
Asymmetric photoreactions of conjugated enones and esters
-
J. P. Pete Asymmetric photoreactions of conjugated enones and esters Adv. Photochem. 1996 21 135 216
-
(1996)
Adv. Photochem.
, vol.21
, pp. 135-216
-
-
Pete, J.P.1
-
6
-
-
0041967557
-
Highly enantioselective Diels-Alder reaction of a photochemically generated o-quinodimethane with olefins
-
B. Grosch C. N. Orlebar E. Herdtweck W. Massa T. Bach Highly enantioselective Diels-Alder reaction of a photochemically generated o-quinodimethane with olefins Angew. Chem. Int. Ed. 2003 42 3693 3696
-
(2003)
Angew. Chem. Int. Ed.
, vol.42
, pp. 3693-3696
-
-
Grosch, B.1
Orlebar, C.N.2
Herdtweck, E.3
Massa, W.4
Bach, T.5
-
8
-
-
24144490444
-
Light on chirality
-
Nobel Lectures, see:
-
Y. Inoue Light on chirality Nature 2005 436 1099 1100
-
(2005)
Nature
, vol.436
, pp. 1099-1100
-
-
Inoue, Y.1
-
9
-
-
0037124758
-
Asymmetric hydrogenations
-
W. S. Knowles Asymmetric hydrogenations Angew. Chem. Int. Ed. 2002 41 1998 2007
-
(2002)
Angew. Chem. Int. Ed.
, vol.41
, pp. 1998-2007
-
-
Knowles, W.S.1
-
10
-
-
0037124885
-
Asymmetric catalysis: Science and opportunities
-
R. Noyori Asymmetric catalysis: science and opportunities Angew. Chem. Int. Ed. 2002 41 2008 2022
-
(2002)
Angew. Chem. Int. Ed.
, vol.41
, pp. 2008-2022
-
-
Noyori, R.1
-
11
-
-
0037124794
-
Searching for new reactivity
-
K. B. Sharpless Searching for new reactivity Angew. Chem. Int. Ed. 2002 41 2024 2032
-
(2002)
Angew. Chem. Int. Ed.
, vol.41
, pp. 2024-2032
-
-
Sharpless, K.B.1
-
12
-
-
33845184415
-
Temperature switching of product chirality upon photosensitized enantiodifferentiating cis-trans isomerization of cyclooctene
-
Y. Inoue T. Yokoyama N. Yamasaki A. Tai Temperature switching of product chirality upon photosensitized enantiodifferentiating cis-trans isomerization of cyclooctene J. Am. Chem. Soc. 1989 111 6480 6482
-
(1989)
J. Am. Chem. Soc.
, vol.111
, pp. 6480-6482
-
-
Inoue, Y.1
Yokoyama, T.2
Yamasaki, N.3
Tai, A.4
-
13
-
-
0001158967
-
An optical yield that increases with temperature in a photochemically induced enantiomeric isomerization
-
Y. Inoue T. Yokoyama N. Yamasaki A. Tai An optical yield that increases with temperature in a photochemically induced enantiomeric isomerization Nature 1989 341 225 226
-
(1989)
Nature
, vol.341
, pp. 225-226
-
-
Inoue, Y.1
Yokoyama, T.2
Yamasaki, N.3
Tai, A.4
-
14
-
-
0001061376
-
Enantiodifferentiating Z-E photoisomerization of cyclooctene sensitized by chiral polyalkyl benzenepolycarboxylates
-
Y. Inoue N. Yamasaki T. Yokoyama A. Tai Enantiodifferentiating Z-E photoisomerization of cyclooctene sensitized by chiral polyalkyl benzenepolycarboxylates J. Org. Chem. 1992 57 1332 1345
-
(1992)
J. Org. Chem.
, vol.57
, pp. 1332-1345
-
-
Inoue, Y.1
Yamasaki, N.2
Yokoyama, T.3
Tai, A.4
-
15
-
-
0000293245
-
Highly enantiodifferentiating photoisomerization of cyclooctene by congested and/or triplex-forming chiral sensitizers
-
Y. Inoue N. Yamasaki T. Yokoyama A. Tai Highly enantiodifferentiating photoisomerization of cyclooctene by congested and/or triplex-forming chiral sensitizers J. Org. Chem. 1993 58 1011 1018
-
(1993)
J. Org. Chem.
, vol.58
, pp. 1011-1018
-
-
Inoue, Y.1
Yamasaki, N.2
Yokoyama, T.3
Tai, A.4
-
16
-
-
0032556204
-
Pressure and temperature control of product chirality in asymmetric photochemistry. Enantiodifferentiating photoisomerization of cyclooctene sensitized by chiral benzenepolycarboxylates
-
Y. Inoue E. Matsushima T. Wada Pressure and temperature control of product chirality in asymmetric photochemistry. Enantiodifferentiating photoisomerization of cyclooctene sensitized by chiral benzenepolycarboxylates J. Am. Chem. Soc. 1998 120 10687 10696
-
(1998)
J. Am. Chem. Soc.
, vol.120
, pp. 10687-10696
-
-
Inoue, Y.1
Matsushima, E.2
Wada, T.3
-
17
-
-
0036259867
-
Discontinuous pressure effect upon enantiodifferentiating photosensitized isomerization of cyclooctene
-
M. Kaneda S. Asaoka H. Ikeda T. Mori T. Wada Y. Inoue Discontinuous pressure effect upon enantiodifferentiating photosensitized isomerization of cyclooctene Chem. Commun. 2002 1272 1273
-
(2002)
Chem. Commun.
, pp. 1272-1273
-
-
Kaneda, M.1
Asaoka, S.2
Ikeda, H.3
Mori, T.4
Wada, T.5
Inoue, Y.6
-
18
-
-
0346907130
-
Pressure control of enantiodifferentiating photoisomerization of cyclooctenes sensitized by chiral benzenepolycarboxylates. the origin of discontinuous pressure dependence of the optical yield
-
M. Kaneda A. Nakamura S. Asaoka H. Ikeda T. Mori T. Wada Y. Inoue Pressure control of enantiodifferentiating photoisomerization of cyclooctenes sensitized by chiral benzenepolycarboxylates. The origin of discontinuous pressure dependence of the optical yield Org. Biomol. Chem. 2003 1 4435 4400
-
(2003)
Org. Biomol. Chem.
, vol.1
, pp. 4435-4400
-
-
Kaneda, M.1
Nakamura, A.2
Asaoka, S.3
Ikeda, H.4
Mori, T.5
Wada, T.6
Inoue, Y.7
-
20
-
-
0034696113
-
Photochirogenesis: Multidimensional control of asymmetric photochemistry
-
Y. Inoue T. Wada S. Asaoka H. Sato J.-P. Pete Photochirogenesis: multidimensional control of asymmetric photochemistry Chem. Commun. 2000 251 259
-
(2000)
Chem. Commun.
, pp. 251-259
-
-
Inoue, Y.1
Wada, T.2
Asaoka, S.3
Sato, H.4
Pete, J.-P.5
-
21
-
-
0035743464
-
Vital role of entropy in photochirogenesis
-
Y. Inoue N. Sugahara T. Wada Vital role of entropy in photochirogenesis Pure Appl. Chem. 2001 73 475 480
-
(2001)
Pure Appl. Chem.
, vol.73
, pp. 475-480
-
-
Inoue, Y.1
Sugahara, N.2
Wada, T.3
-
22
-
-
0023178396
-
Regio- and stereoselective photodimerization of anthracene derivatives included by cyclodextrins
-
T. Tamaki T. Kokubo K. Ichimura Regio- and stereoselective photodimerization of anthracene derivatives included by cyclodextrins Tetrahedron 1987 43 1485 1494
-
(1987)
Tetrahedron
, vol.43
, pp. 1485-1494
-
-
Tamaki, T.1
Kokubo, T.2
Ichimura, K.3
-
23
-
-
0001362634
-
Asymmetric induction in benzoin by photolysis of benzaldehyde adsorbed in cyclodextrin cavities
-
V. P. Rao N. J. Turro Asymmetric induction in benzoin by photolysis of benzaldehyde adsorbed in cyclodextrin cavities Tetrahedron Lett. 1989 30 4641 4644
-
(1989)
Tetrahedron Lett.
, vol.30
, pp. 4641-4644
-
-
Rao, V.P.1
Turro, N.J.2
-
24
-
-
0033812690
-
Asymmetric induction with cyclodextrins: Photocyclization of tropolone alkyl ethers
-
S. Koodanjeri A. Joy V. Ramamurthy Asymmetric induction with cyclodextrins: photocyclization of tropolone alkyl ethers Tetrahedron 2000 56 7003 7009
-
(2000)
Tetrahedron
, vol.56
, pp. 7003-7009
-
-
Koodanjeri, S.1
Joy, A.2
Ramamurthy, V.3
-
25
-
-
0035912303
-
Asymmetric induction in intramolecular meta photocycloaddition: Cyclodextrin-mediated solid-phase photochemistry of various phenoxyalkenes
-
K. Vízvárdi K. Desmet I. Luyten P. Sandra G. Hoornaert E. V. Eycken Asymmetric induction in intramolecular meta photocycloaddition: cyclodextrin-mediated solid-phase photochemistry of various phenoxyalkenes Org. Lett. 2001 3 1173 1175
-
(2001)
Org. Lett.
, vol.3
, pp. 1173-1175
-
-
Vízvárdi, K.1
Desmet, K.2
Luyten, I.3
Sandra, P.4
Hoornaert, G.5
Eycken, E.V.6
-
26
-
-
0037049190
-
Cyclodextrin mediated enantio and diastereoselective geometric photoisomerization of diphenylcyclopropane and its derivatives
-
S. Koodanjeri V. Ramamurthy Cyclodextrin mediated enantio and diastereoselective geometric photoisomerization of diphenylcyclopropane and its derivatives Tetrahedron Lett. 2002 43 9229 9232
-
(2002)
Tetrahedron Lett.
, vol.43
, pp. 9229-9232
-
-
Koodanjeri, S.1
Ramamurthy, V.2
-
27
-
-
0037121566
-
Cyclodextrin mediated solvent-free enantioselective photocyclization of N-alkyl pyridones
-
J. Shailaja S. Karthikeyan V. Ramamurthy Cyclodextrin mediated solvent-free enantioselective photocyclization of N-alkyl pyridones Tetrahedron Lett. 2002 43 9335 9339
-
(2002)
Tetrahedron Lett.
, vol.43
, pp. 9335-9339
-
-
Shailaja, J.1
Karthikeyan, S.2
Ramamurthy, V.3
-
28
-
-
13844308321
-
Template-assisted stereoselective photocyclodimerization of 2-anthracenecarboxylic acid by bispyridinio-appended γ-cyclodextrin
-
H. Ikeda T. Nihei A. Ueno Template-assisted stereoselective photocyclodimerization of 2-anthracenecarboxylic acid by bispyridinio-appended γ-cyclodextrin J. Org. Chem. 2005 70 1237 1242
-
(2005)
J. Org. Chem.
, vol.70
, pp. 1237-1242
-
-
Ikeda, H.1
Nihei, T.2
Ueno, A.3
-
29
-
-
33644675697
-
Asymmetric [2 + 2] photocycloaddition of cycloalkenone-cyclodextrin complexes to ethylene
-
A. Furutani K. Katayama Y. Ueshima M. Ogura Y. Tobe H. Kurosawa K. Tsutsumi T. Morimoto K. Kakiuchi Asymmetric [2 + 2] photocycloaddition of cycloalkenone-cyclodextrin complexes to ethylene Chirality 2006 18 217 221
-
(2006)
Chirality
, vol.18
, pp. 217-221
-
-
Furutani, A.1
Katayama, K.2
Ueshima, Y.3
Ogura, M.4
Tobe, Y.5
Kurosawa, H.6
Tsutsumi, K.7
Morimoto, T.8
Kakiuchi, K.9
-
30
-
-
0001677328
-
Inclusion-enhanced optical yield and E/Z ratio in enantiodifferentiating photoisomerization of cyclooctene included and sensitized by β-cyclodextrin monobenzoate
-
Y. Inoue F. Dong K. Yamamoto L.-H. Tong H. Tsuneishi T. Hakushi A. Tai Inclusion-enhanced optical yield and E/Z ratio in enantiodifferentiating photoisomerization of cyclooctene included and sensitized by β-cyclodextrin monobenzoate J. Am. Chem. Soc. 1995 117 11033 11034
-
(1995)
J. Am. Chem. Soc.
, vol.117
, pp. 11033-11034
-
-
Inoue, Y.1
Dong, F.2
Yamamoto, K.3
Tong, L.-H.4
Tsuneishi, H.5
Hakushi, T.6
Tai, A.7
-
31
-
-
0034680615
-
Supramolecular photochirogenesis. 2. Enantiodifferentiating photoisomerization of cyclooctene included and sensitized by 6-O-modified cyclodextrins
-
Y. Inoue T. Wada N. Sugahara K. Yamamoto K. Kimura L.-H. Tong X.-M. Gao Z.-J. Hou Y. Liu Supramolecular photochirogenesis. 2. Enantiodifferentiating photoisomerization of cyclooctene included and sensitized by 6-O-modified cyclodextrins J. Org. Chem. 2000 65 8041 8050
-
(2000)
J. Org. Chem.
, vol.65
, pp. 8041-8050
-
-
Inoue, Y.1
Wada, T.2
Sugahara, N.3
Yamamoto, K.4
Kimura, K.5
Tong, L.-H.6
Gao, X.-M.7
Hou, Z.-J.8
Liu, Y.9
-
32
-
-
12344312075
-
Supramolecular photochirogenesis. 3. Enantiodifferentiating photoisomerization of cyclooctene included and sensitized by 6-O-mono(o-methoxybenzoyl)-β-cyclodextrin
-
Y. Gao M. Inoue T. Wada Y. Inoue Supramolecular photochirogenesis. 3. Enantiodifferentiating photoisomerization of cyclooctene included and sensitized by 6-O-mono(o-methoxybenzoyl)-β-cyclodextrin J. Incl. Phenom. Macrocycl. Chem. 2004 50 111 114
-
(2004)
J. Incl. Phenom. Macrocycl. Chem.
, vol.50
, pp. 111-114
-
-
Gao, Y.1
Inoue, M.2
Wada, T.3
Inoue, Y.4
-
33
-
-
37749023584
-
Supramolecular enantiodifferentiating photoisomerization of cyclooctene with modified β-cyclodextrins: Critical control by a host structure
-
R. Lu C. Yang Y. Cao Z. Wang T. Wada W. Jiao T. Mori Y. Inoue Supramolecular enantiodifferentiating photoisomerization of cyclooctene with modified β-cyclodextrins: critical control by a host structure Chem. Commun. 2008 374 376
-
(2008)
Chem. Commun.
, pp. 374-376
-
-
Lu, R.1
Yang, C.2
Cao, Y.3
Wang, Z.4
Wada, T.5
Jiao, W.6
Mori, T.7
Inoue, Y.8
-
34
-
-
20444473216
-
Enantioselective photoelectrocyclization within zeolites: Tropolone methyl ether in chirally modified NaY
-
A. Joy V. Ramamurthy J. R. Scheffer D. R. Corbin Enantioselective photoelectrocyclization within zeolites: tropolone methyl ether in chirally modified NaY J. Chem. Soc., Chem. Commun. 1998 1379 1380
-
(1998)
J. Chem. Soc., Chem. Commun.
, pp. 1379-1380
-
-
Joy, A.1
Ramamurthy, V.2
Scheffer, J.R.3
Corbin, D.R.4
-
35
-
-
0001458354
-
Chirally modified zeolites as reaction media: Photochemistry of an achiral tropolone ether
-
A. Joy R. Scheffer V. Ramamurthy Chirally modified zeolites as reaction media: photochemistry of an achiral tropolone ether Org. Lett. 2000 2 119 121
-
(2000)
Org. Lett.
, vol.2
, pp. 119-121
-
-
Joy, A.1
Scheffer, R.2
Ramamurthy, V.3
-
36
-
-
0033802167
-
From boiling stones to smart crystals: Supramolecular and magnetic isotope control of radical-radical reactions in zeolites
-
N. J. Turro From boiling stones to smart crystals: supramolecular and magnetic isotope control of radical-radical reactions in zeolites Acc. Chem. Res. 2000 33 637 646
-
(2000)
Acc. Chem. Res.
, vol.33
, pp. 637-646
-
-
Turro, N.J.1
-
37
-
-
0035929347
-
First photosensitized enantiodifferentiating isomerization by optically active sensitizer immobilized in zeolite supercages
-
T. Wada M. Shikimi Y. Inoue G. Lem N. J. Turro First photosensitized enantiodifferentiating isomerization by optically active sensitizer immobilized in zeolite supercages Chem. Commun. 2001 1864 1865
-
(2001)
Chem. Commun.
, pp. 1864-1865
-
-
Wada, T.1
Shikimi, M.2
Inoue, Y.3
Lem, G.4
Turro, N.J.5
-
40
-
-
4444220353
-
Stereocontrol within confined spaces: Enantioselective photooxidation of enecarbamates inside zeolites supercages
-
J. Sivaguru T. Poon R. Franz S. Jockusch W. Adam N. J. Turro Stereocontrol within confined spaces: enantioselective photooxidation of enecarbamates inside zeolites supercages J. Am. Chem. Soc. 2004 126 10816 10817
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 10816-10817
-
-
Sivaguru, J.1
Poon, T.2
Franz, R.3
Jockusch, S.4
Adam, W.5
Turro, N.J.6
-
41
-
-
33644775962
-
Control of chirality by cations in confined spaces: Photooxidation of enecarbamates inside zeolite supercages
-
J. Sivaguru H. Saito M. R. Solomon L. S. Kaanumalle T. Poon S. Jockusch W. Adam V. Ramamurthy Y. Inoue N. J. Turro Control of chirality by cations in confined spaces: photooxidation of enecarbamates inside zeolite supercages Photochem. Photobiol. 2006 82 123 131
-
(2006)
Photochem. Photobiol.
, vol.82
, pp. 123-131
-
-
Sivaguru, J.1
Saito, H.2
Solomon, M.R.3
Kaanumalle, L.S.4
Poon, T.5
Jockusch, S.6
Adam, W.7
Ramamurthy, V.8
Inoue, Y.9
Turro, N.J.10
-
42
-
-
34250737922
-
Value of zeolites in asymmetric induction during photocyclization of pyridones, cyclohexadienones and naphthalenones
-
K. Sivasubramanian L. S. Kaanumalle S. Uppili V. Ramamurthy Value of zeolites in asymmetric induction during photocyclization of pyridones, cyclohexadienones and naphthalenones Org. Biomol. Chem. 2007 5 1569 1576
-
(2007)
Org. Biomol. Chem.
, vol.5
, pp. 1569-1576
-
-
Sivasubramanian, K.1
Kaanumalle, L.S.2
Uppili, S.3
Ramamurthy, V.4
-
43
-
-
25144459418
-
Entropy-controlled supramolecular photochirogenesis: Enantiodifferentiating Z-E photoisomerization of cyclooctene included and sensitized by permethylated 6-O-benzoyl-β-cyclodextrin
-
G. Fukuhara T. Mori T. Wada Y. Inoue Entropy-controlled supramolecular photochirogenesis: enantiodifferentiating Z-E photoisomerization of cyclooctene included and sensitized by permethylated 6-O-benzoyl-β-cyclodextrin Chem. Commun. 2005 4199 4201
-
(2005)
Chem. Commun.
, pp. 4199-4201
-
-
Fukuhara, G.1
Mori, T.2
Wada, T.3
Inoue, Y.4
-
44
-
-
33645792786
-
Pressure and temperature-controlled enantiodifferentiating [4 + 4] photocyclodimerization of 2-anthracenecarboxylate mediated by secondary face- and skeleton-modified γ-cyclodextrins
-
C. Yang A. Nakamura G. Fukuhara Y. Origane T. Mori T. Wada Y. Inoue Pressure and temperature-controlled enantiodifferentiating [4 + 4] photocyclodimerization of 2-anthracenecarboxylate mediated by secondary face- and skeleton-modified γ-cyclodextrins J. Org. Chem. 2006 71 3126 3136
-
(2006)
J. Org. Chem.
, vol.71
, pp. 3126-3136
-
-
Yang, C.1
Nakamura, A.2
Fukuhara, G.3
Origane, Y.4
Mori, T.5
Wada, T.6
Inoue, Y.7
-
45
-
-
33646937413
-
The first supramolecular photosensitization of enantiodifferentiating bimolecular reaction: Anti-Markovnikov photoaddition of methanol to 1,1-diphenylpropene sensitized by modified β-cyclodextrin
-
G. Fukuhara T. Mori T. Wada Y. Inoue The first supramolecular photosensitization of enantiodifferentiating bimolecular reaction: anti-Markovnikov photoaddition of methanol to 1,1-diphenylpropene sensitized by modified β-cyclodextrin Chem. Commun. 2006 1712 1714
-
(2006)
Chem. Commun.
, pp. 1712-1714
-
-
Fukuhara, G.1
Mori, T.2
Wada, T.3
Inoue, Y.4
-
46
-
-
33750025006
-
Entropy-controlled supramolecular photochirogenesis: Enantiodifferentiating Z-E photoisomerization of cyclooctene included and sensitized by permethylated 6-O-modified β-cyclodextrins
-
G. Fukuhara T. Mori T. Wada Y. Inoue Entropy-controlled supramolecular photochirogenesis: enantiodifferentiating Z-E photoisomerization of cyclooctene included and sensitized by permethylated 6-O-modified β-cyclodextrins J. Org. Chem. 2006 71 8233 8243
-
(2006)
J. Org. Chem.
, vol.71
, pp. 8233-8243
-
-
Fukuhara, G.1
Mori, T.2
Wada, T.3
Inoue, Y.4
-
47
-
-
34248372816
-
Supramolecular enantiodifferentiating photoisomerization of (Z,Z)-1,3-cyclooctadiene included and sensitized by naphthalene-modified cyclodextrins
-
C. Yang T. Mori T. Wada Y. Inoue Supramolecular enantiodifferentiating photoisomerization of (Z,Z)-1,3-cyclooctadiene included and sensitized by naphthalene-modified cyclodextrins New J. Chem. 2007 31 697 702
-
(2007)
New J. Chem.
, vol.31
, pp. 697-702
-
-
Yang, C.1
Mori, T.2
Wada, T.3
Inoue, Y.4
-
48
-
-
34250745339
-
Inherently chiral molecular clips: Synthesis, chiroptical properties, and application to chiral discrimination
-
Other type of chiral MCs, see:
-
G. Fukuhara S. Madenci J. Polkowska F. Bastkowski F.-G. Klärner Y. Origane M. Kaneda T. Mori T. Wada Y. Inoue Inherently chiral molecular clips: synthesis, chiroptical properties, and application to chiral discrimination Chem. Eur. J. 2007 13 2473 2479
-
(2007)
Chem. Eur. J.
, vol.13
, pp. 2473-2479
-
-
Fukuhara, G.1
Madenci, S.2
Polkowska, J.3
Bastkowski, F.4
Klärner, F.-G.5
Origane, Y.6
Kaneda, M.7
Mori, T.8
Wada, T.9
Inoue, Y.10
-
49
-
-
0000148654
-
Tröger's base analogs. New structural units for the preparation of chiral hosts and metal ligands
-
C. S. Wilcox Tröger's base analogs. New structural units for the preparation of chiral hosts and metal ligands Tetrahedron Lett. 1985 26 5749 5752
-
(1985)
Tetrahedron Lett.
, vol.26
, pp. 5749-5752
-
-
Wilcox, C.S.1
-
50
-
-
0001086648
-
Synthesis of chiral molecular clefts. New armatures for biomimetic systems
-
C. S. Wilcox L. M. Greer V. Lynch Synthesis of chiral molecular clefts. New armatures for biomimetic systems J. Am. Chem. Soc. 1987 109 1865 1867
-
(1987)
J. Am. Chem. Soc.
, vol.109
, pp. 1865-1867
-
-
Wilcox, C.S.1
Greer, L.M.2
Lynch, V.3
-
51
-
-
0001076770
-
Molecular clefts. 1. Synthetic methodology for the preparation of analogues of Kagan's ether
-
M. Harmata T. Murray Molecular clefts. 1. Synthetic methodology for the preparation of analogues of Kagan's ether J. Org. Chem. 1989 54 3761 3763
-
(1989)
J. Org. Chem.
, vol.54
, pp. 3761-3763
-
-
Harmata, M.1
Murray, T.2
-
52
-
-
33845184812
-
Chiral recognition in clefts and cyclophane cavities shaped by the 1,1′-binaphthyl major groove
-
P. P. Castro T. M. Georgiadis F. Diederich Chiral recognition in clefts and cyclophane cavities shaped by the 1,1′-binaphthyl major groove J. Org. Chem. 1989 54 5835 5838
-
(1989)
J. Org. Chem.
, vol.54
, pp. 5835-5838
-
-
Castro, P.P.1
Georgiadis, T.M.2
Diederich, F.3
-
53
-
-
0025261205
-
Molecular clefts 2. An analogue of Kagan's ether as a molecular cleft: Synthesis and clathrate formation with ethyl acetate
-
M. Harmata C. L. Barnes Molecular clefts 2. An analogue of Kagan's ether as a molecular cleft: synthesis and clathrate formation with ethyl acetate Tetrahedron Lett. 1990 31 1825 1828
-
(1990)
Tetrahedron Lett.
, vol.31
, pp. 1825-1828
-
-
Harmata, M.1
Barnes, C.L.2
-
54
-
-
0000556121
-
Molecular clefts. 3. the crystal structure of a chiral molecular tweezer and its guest
-
M. Harmata C. L. Barnes Molecular clefts. 3. The crystal structure of a chiral molecular tweezer and its guest J. Am. Chem. Soc. 1990 112 5655 5657
-
(1990)
J. Am. Chem. Soc.
, vol.112
, pp. 5655-5657
-
-
Harmata, M.1
Barnes, C.L.2
-
55
-
-
0025915905
-
Selective α,ω-dicarboxylic acid recognition in a chiral cleft shaped by the 9,9′-spirobifluorene unit
-
V. A. Montero L. Tomlinson K. N. Houk F. Diederich Selective α,ω-dicarboxylic acid recognition in a chiral cleft shaped by the 9,9′-spirobifluorene unit Tetrahedron Lett. 1991 32 5309 5312
-
(1991)
Tetrahedron Lett.
, vol.32
, pp. 5309-5312
-
-
Montero, V.A.1
Tomlinson, L.2
Houk, K.N.3
Diederich, F.4
-
56
-
-
0029130006
-
Chiral 1,1′-binaphthyl molecular clefts for the complexation of excitatory amino-acid derivatives
-
E. Martinborough T. M. Denti P. P. Castro T. B. Wyman C. B. Knobler F. Diederich Chiral 1,1′-binaphthyl molecular clefts for the complexation of excitatory amino-acid derivatives Helv. Chim. Acta 1995 78 1037 1066
-
(1995)
Helv. Chim. Acta
, vol.78
, pp. 1037-1066
-
-
Martinborough, E.1
Denti, T.M.2
Castro, P.P.3
Wyman, T.B.4
Knobler, C.B.5
Diederich, F.6
-
57
-
-
0001301987
-
Design, synthesis, and evaluation of bile acid-based molecular tweezers
-
L. J. D'Souza U. Maitra Design, synthesis, and evaluation of bile acid-based molecular tweezers J. Org. Chem. 1996 61 9494 9502
-
(1996)
J. Org. Chem.
, vol.61
, pp. 9494-9502
-
-
D'Souza, L.J.1
Maitra, U.2
-
58
-
-
0030833068
-
The determination of the absolute configuration of a chiral molecular tweezer using CD spectroscopy
-
J. Fleischhauer M. Harmata M. Kahraman A. Koslowski C. J. Welch The determination of the absolute configuration of a chiral molecular tweezer using CD spectroscopy Tetrahedron Lett. 1997 38 8655 8658
-
(1997)
Tetrahedron Lett.
, vol.38
, pp. 8655-8658
-
-
Fleischhauer, J.1
Harmata, M.2
Kahraman, M.3
Koslowski, A.4
Welch, C.J.5
-
59
-
-
0032516378
-
Solvent effect in molecular recognition: Determining binding constants in different solvents following an extraction based protocol
-
U. Maitra P. Rao V. Kurmar P. R. Balasubramanian L. Mathew Solvent effect in molecular recognition: determining binding constants in different solvents following an extraction based protocol Tetrahedron Lett. 1998 39 3255 3258
-
(1998)
Tetrahedron Lett.
, vol.39
, pp. 3255-3258
-
-
Maitra, U.1
Rao, P.2
Kurmar, V.3
Balasubramanian, P.R.4
Mathew, L.5
-
60
-
-
0034685996
-
Synthesis of functionalized chiral carbocyclic cleft molecules complementary to Tröger's base derivatives
-
M. C. Kimber A. C. Try L. Painter M. M. Harding P. Turner Synthesis of functionalized chiral carbocyclic cleft molecules complementary to Tröger's base derivatives J. Org. Chem. 2000 65 3042 3046
-
(2000)
J. Org. Chem.
, vol.65
, pp. 3042-3046
-
-
Kimber, M.C.1
Try, A.C.2
Painter, L.3
Harding, M.M.4
Turner, P.5
-
61
-
-
0034680655
-
Bile acid-derived molecular tweezers: Study of solvent effects in binding, and determination of thermodynamic parameters by an extraction-based protocol
-
V. K. Potluri U. Maitra Bile acid-derived molecular tweezers: study of solvent effects in binding, and determination of thermodynamic parameters by an extraction-based protocol J. Org. Chem. 2000 65 7764 7769
-
(2000)
J. Org. Chem.
, vol.65
, pp. 7764-7769
-
-
Potluri, V.K.1
Maitra, U.2
-
64
-
-
0344153826
-
Homochiral molecular tweezers as hosts for the highly enantioselective recognition of amino acid derivatives
-
C.-P. Du J.-S. You X.-Q. Yu C.-L. Liu J.-B. Lan R.-G. Xie Homochiral molecular tweezers as hosts for the highly enantioselective recognition of amino acid derivatives Tetrahedron: Asymmetry 2003 14 3651 3656
-
(2003)
Tetrahedron: Asymmetry
, vol.14
, pp. 3651-3656
-
-
Du, C.-P.1
You, J.-S.2
Yu, X.-Q.3
Liu, C.-L.4
Lan, J.-B.5
Xie, R.-G.6
-
66
-
-
9444250434
-
Chiral molecular tweezers
-
M. Harmata Chiral molecular tweezers Acc. Chem. Res. 2004 37 862 873
-
(2004)
Acc. Chem. Res.
, vol.37
, pp. 862-873
-
-
Harmata, M.1
-
67
-
-
22144451402
-
Use of Tröger's base as a scaffold for new chiral molecular tweezers: Synthesis of trimeric, fused Tröger's bases
-
T. Mas C. Pardo J. Elguero Use of Tröger's base as a scaffold for new chiral molecular tweezers: synthesis of trimeric, fused Tröger's bases Helv. Chim. Acta 2005 88 1199 1207
-
(2005)
Helv. Chim. Acta
, vol.88
, pp. 1199-1207
-
-
Mas, T.1
Pardo, C.2
Elguero, J.3
-
68
-
-
24944488504
-
Highly sensitive chiral shift reagent bearing two zinc porphyrins
-
T. Ema N. Ouchi T. Doi T. Korenaga T. Sakai Highly sensitive chiral shift reagent bearing two zinc porphyrins Org. Lett. 2005 7 3985 3988
-
(2005)
Org. Lett.
, vol.7
, pp. 3985-3988
-
-
Ema, T.1
Ouchi, N.2
Doi, T.3
Korenaga, T.4
Sakai, T.5
-
69
-
-
33645323769
-
The synthesis and characterization of all diastereomers of a linear symmetrically fused tris-Tröger's base analogue: New chiral cleft compounds
-
J. Artacho P. Nilsson K.-E. Bergquist O. F. Wendt K. Wärnmark The synthesis and characterization of all diastereomers of a linear symmetrically fused tris-Tröger's base analogue: new chiral cleft compounds Chem. Eur. J. 2006 12 2692 2701
-
(2006)
Chem. Eur. J.
, vol.12
, pp. 2692-2701
-
-
Artacho, J.1
Nilsson, P.2
Bergquist, K.-E.3
Wendt, O.F.4
Wärnmark, K.5
-
70
-
-
33646022265
-
Synthesis and X-ray crystallographic analysis of chiral pyridyl substituted carbocyclic molecular clefts
-
C. K. Y. Lee J. L. Groneman P. Turner L. M. Rendina M. M. Harding Synthesis and X-ray crystallographic analysis of chiral pyridyl substituted carbocyclic molecular clefts Tetrahedron 2006 62 4870 4878
-
(2006)
Tetrahedron
, vol.62
, pp. 4870-4878
-
-
Lee, C.K.Y.1
Groneman, J.L.2
Turner, P.3
Rendina, L.M.4
Harding, M.M.5
-
71
-
-
33646267714
-
New chiral benzothiazine ligand and its use in the synthesis of a chiral receptor
-
M. Harmata N. L. Calkins R. G. Baughman C. L. Barnes New chiral benzothiazine ligand and its use in the synthesis of a chiral receptor J. Org. Chem. 2006 71 3650 3652
-
(2006)
J. Org. Chem.
, vol.71
, pp. 3650-3652
-
-
Harmata, M.1
Calkins, N.L.2
Baughman, R.G.3
Barnes, C.L.4
-
72
-
-
33750010592
-
Di-(R,R)-1-[10-(1-hydroxy-2,2,2-trifluoroethyl)-9-anthryl]-2,2, 2-trifluoroethyl muconate: A highly chiral cavity for enantiodiscrimination by NMR
-
M. Palomino-Schätzlein A. Virgili S. Gil C. Jaime Di-(R,R)-1-[10-(1-hydroxy-2,2,2-trifluoroethyl)-9-anthryl]-2,2,2-trifluoroethyl muconate: a highly chiral cavity for enantiodiscrimination by NMR J. Org. Chem. 2006 71 8114 8120
-
(2006)
J. Org. Chem.
, vol.71
, pp. 8114-8120
-
-
Palomino-Schätzlein, M.1
Virgili, A.2
Gil, S.3
Jaime, C.4
-
73
-
-
34249316163
-
Chiral molecular clips control orthogonal crystalline organization
-
Y. Chen N. She X. Meng G. Yin A. Wu L. Isaacs Chiral molecular clips control orthogonal crystalline organization Org. Lett. 2007 9 1899 1902
-
(2007)
Org. Lett.
, vol.9
, pp. 1899-1902
-
-
Chen, Y.1
She, N.2
Meng, X.3
Yin, G.4
Wu, A.5
Isaacs, L.6
-
74
-
-
34247573471
-
Cleft molecules as organocatalysts in an asymmetric hetero-Diels-Alder reaction
-
For (Z,Z)-1,3-cyclooctadiene, see:
-
A. Friberg C. Olsson F. Ek U. Berg T. Frejd Cleft molecules as organocatalysts in an asymmetric hetero-Diels-Alder reaction Tetrahedron: Asymmetry 2007 18 885 891
-
(2007)
Tetrahedron: Asymmetry
, vol.18
, pp. 885-891
-
-
Friberg, A.1
Olsson, C.2
Ek, F.3
Berg, U.4
Frejd, T.5
-
75
-
-
0031017644
-
Optically active (E,Z)-1,3-cyclooctadiene: First enantioselective synthesis through asymmetric photosensitization and chiroptical property
-
Y. Inoue H. Tsuneishi T. Hakushi A. Tai Optically active (E,Z)-1,3-cyclooctadiene: first enantioselective synthesis through asymmetric photosensitization and chiroptical property J. Am. Chem. Soc. 1997 119 472 478
-
(1997)
J. Am. Chem. Soc.
, vol.119
, pp. 472-478
-
-
Inoue, Y.1
Tsuneishi, H.2
Hakushi, T.3
Tai, A.4
-
76
-
-
0004393799
-
Enantiodifferentiating photoisomerization of (Z)-cyclooctene and (Z,Z)-cycloocta-1,3-diene sensitized by chiral aromatic amides
-
For 1,1-diphenylpropene, see:
-
M. Shi Y. Inoue Enantiodifferentiating photoisomerization of (Z)-cyclooctene and (Z,Z)-cycloocta-1,3-diene sensitized by chiral aromatic amides J. Chem. Soc., Perkin Trans. 2 1998 1725 1729
-
(1998)
J. Chem. Soc., Perkin Trans. 2
, pp. 1725-1729
-
-
Shi, M.1
Inoue, Y.2
-
77
-
-
0033595490
-
Enantiodifferentiating anti-Markovnikov photoaddition of alcohols to 1,1-diphenylalkenes sensitized by chiral naphthalenecarboxylates
-
S. Asaoka T. Kitazawa T. Wada Y. Inoue Enantiodifferentiating anti-Markovnikov photoaddition of alcohols to 1,1-diphenylalkenes sensitized by chiral naphthalenecarboxylates J. Am. Chem. Soc. 1999 121 8486 8498
-
(1999)
J. Am. Chem. Soc.
, vol.121
, pp. 8486-8498
-
-
Asaoka, S.1
Kitazawa, T.2
Wada, T.3
Inoue, Y.4
-
78
-
-
0037433567
-
Microenvironmental polarity control of electron-transfer photochirogenesis. Enantiodifferentiating polar addition of 1,1-diphenyl-1- alkenes photosensitized by saccharide naphthalenecarboxylates
-
S. Asaoka T Wada Y. Inoue Microenvironmental polarity control of electron-transfer photochirogenesis. Enantiodifferentiating polar addition of 1,1-diphenyl-1-alkenes photosensitized by saccharide naphthalenecarboxylates J. Am. Chem. Soc. 2003 125 3008 3027
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 3008-3027
-
-
Asaoka, S.1
Wada, T.2
Inoue, Y.3
-
80
-
-
12444325515
-
+ in water
-
+ in water Chem. Eur. J. 2005 11 477 494
-
(2005)
Chem. Eur. J.
, vol.11
, pp. 477-494
-
-
Fokkens, M.1
Jasper, C.2
Schrader, T.3
Koziol, F.4
Ochsenfeld, C.5
Polkowska, J.6
Lobert, M.7
Kahlert, B.8
Klärner, F.-G.9
-
84
-
-
0000237862
-
Thermodynamics of the binding of biotin and some analogues by avidin
-
N. M. Green Thermodynamics of the binding of biotin and some analogues by avidin Biochem. J. 1966 101. 774 780
-
(1966)
Biochem. J.
, vol.101
, pp. 774-780
-
-
Green, N.M.1
-
85
-
-
25144489591
-
Complexation of ferrocene derivatives by the cucurbit[7]uril host: A comparative study of the cucurbituril and cyclodextrin host families
-
W. S. Jeon K. Moon S. H. Park H. Chun Y. H. Ko J. Y. Lee E. S. Lee S. Samal N. Selvapalam M. V. Rekharsky V. Sindelar D. Sobransingh Y. Inoue A. E. Kaifer K. Kim Complexation of ferrocene derivatives by the cucurbit[7]uril host: a comparative study of the cucurbituril and cyclodextrin host families J. Am. Chem. Soc. 2005 127 12984 12989
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 12984-12989
-
-
Jeon, W.S.1
Moon, K.2
Park, S.H.3
Chun, H.4
Ko, Y.H.5
Lee, J.Y.6
Lee, E.S.7
Samal, S.8
Selvapalam, N.9
Rekharsky, M.V.10
Sindelar, V.11
Sobransingh, D.12
Inoue, Y.13
Kaifer, A.E.14
Kim, K.15
-
86
-
-
38049144318
-
A synthetic host-guest system achieves avidin-biotin affinity by overcoming enthalpy-entropy compensation
-
These thermodynamic parameters are considerably large compared with those of typical cyclodextrin complexations that Rekharsky and Inoue previously demonstrated; see:
-
M. V. Rekharsky T. Mori C. Yang Y. H. Ko N. Selvapalam H. Kim D. Sobransingh A. E. Kaifer S. Liu L. Isaacs W. Chen S. Moghaddam M. K. Gilson K. Kim Y. Inoue A synthetic host-guest system achieves avidin-biotin affinity by overcoming enthalpy-entropy compensation Proc. Natl. Acad. Sci. USA 2007 104 20737 20742
-
(2007)
Proc. Natl. Acad. Sci. USA
, vol.104
, pp. 20737-20742
-
-
Rekharsky, M.V.1
Mori, T.2
Yang, C.3
Ko, Y.H.4
Selvapalam, N.5
Kim, H.6
Sobransingh, D.7
Kaifer, A.E.8
Liu, S.9
Isaacs, L.10
Chen, W.11
Moghaddam, S.12
Gilson, M.K.13
Kim, K.14
Inoue, Y.15
-
87
-
-
4243778369
-
Complexation thermodynamics of cyclodextrins
-
M. V. Rekharsky Y. Inoue Complexation thermodynamics of cyclodextrins Chem. Rev. 1998 98 1875 1917
-
(1998)
Chem. Rev.
, vol.98
, pp. 1875-1917
-
-
Rekharsky, M.V.1
Inoue, Y.2
-
89
-
-
56849104305
-
Photochemical reactions of aromatic compounds. XXXI. Exciplex, quenching by pyridine, methylated pyridines, and methylated imidazoles and termolecular interaction in the excited singlet state
-
T. Majima C. Pac H. Sakurai Photochemical reactions of aromatic compounds. XXXI. Exciplex, quenching by pyridine, methylated pyridines, and methylated imidazoles and termolecular interaction in the excited singlet state Bull. Chem. Soc. Jpn. 1978 51 1811 1817
-
(1978)
Bull. Chem. Soc. Jpn.
, vol.51
, pp. 1811-1817
-
-
Majima, T.1
Pac, C.2
Sakurai, H.3
-
90
-
-
0011538980
-
Exciplex quenching. Geometric and electronic requirements
-
R. A. Caldwell D. Creed H. Ohta Exciplex quenching. Geometric and electronic requirements J. Am. Chem. Soc. 1975 97 3246 3247
-
(1975)
J. Am. Chem. Soc.
, vol.97
, pp. 3246-3247
-
-
Caldwell, R.A.1
Creed, D.2
Ohta, H.3
|