-
1
-
-
52449134005
-
Asymmetric intramolecular arylcyanation of unactivated olefins via C-CN bond activation
-
Watson, M. P. & Jacobsen, E. N. Asymmetric intramolecular arylcyanation of unactivated olefins via C-CN bond activation. J. Am. Chem. Soc. 130, 12594-12595 (2008).
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 12594-12595
-
-
Watson, M.P.1
Jacobsen, E.N.2
-
2
-
-
23044496800
-
Catalytic enantioselective Negishi reactions of racemic secondary benzylic halides
-
Arp, F. O. & Fu, G. C. Catalytic enantioselective Negishi reactions of racemic secondary benzylic halides. J. Am. Chem. Soc. 127, 10482-10483 (2005).
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 10482-10483
-
-
Arp, F.O.1
Fu, G.C.2
-
3
-
-
70449575808
-
Enantioselective palladium-catalyzed direct arylations at ambient temperature: Access to indanes with quaternary stereocenters
-
Albicker, M. & Cramer, N. Enantioselective palladium-catalyzed direct arylations at ambient temperature: access to indanes with quaternary stereocenters. Angew. Chem. Int. Ed. 48, 9139-9142 (2009).
-
(2009)
Angew. Chem. Int. Ed.
, vol.48
, pp. 9139-9142
-
-
Albicker, M.1
Cramer, N.2
-
4
-
-
84859250819
-
Diastereo- and enantioselective intramolecular C(sp3)?H arylation for the synthesis of fused cyclopentanes
-
Martin, N., Pierre, C., Davi, M., Jazzar, R. & Baudoin, O. Diastereo- and enantioselective intramolecular C(sp3)?H arylation for the synthesis of fused cyclopentanes. Chem. Eur. J. 18, 4480-4484 (2012).
-
(2012)
Chem. Eur. J.
, vol.18
, pp. 4480-4484
-
-
Martin, N.1
Pierre, C.2
Davi, M.3
Jazzar, R.4
Baudoin, O.5
-
5
-
-
27544489337
-
Catalytic asymmetric reductive Michael cyclization
-
Yang, J.W., Hechavarria Fonseca, M. T. & List, B. Catalytic asymmetric reductive Michael cyclization. J. Am. Chem. Soc. 127, 15036-15037 (2005).
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 15036-15037
-
-
Yang, J.W.1
Hechavarria Fonseca, M.T.2
List, B.3
-
6
-
-
79952269315
-
Organocatalytic functionalization of carboxylic acids: Isothiourea-catalyzed asymmetric intra- and intermolecular Michael addition-lactonizations
-
Belmessieri, D., Morrill, L. C., Simal, C., Slawin, A. M. Z. & Smith, A. D. Organocatalytic functionalization of carboxylic acids: isothiourea-catalyzed asymmetric intra- and intermolecular Michael addition-lactonizations. J. Am. Chem. Soc. 133, 2714-2720 (2011).
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 2714-2720
-
-
Belmessieri, D.1
Morrill, L.C.2
Simal, C.3
Slawin, A.M.Z.4
Smith, A.D.5
-
7
-
-
34250822311
-
A highly enantioselective intramolecular Michael reaction catalyzed by N-heterocyclic carbenes
-
Phillips, E. M., Wadamoto, M., Chan, A. & Scheidt, K. A. A highly enantioselective intramolecular Michael reaction catalyzed by N-heterocyclic carbenes. Angew. Chem. Int. Ed. 46, 3107-3110 (2007).
-
(2007)
Angew. Chem. Int. Ed.
, vol.46
, pp. 3107-3110
-
-
Phillips, E.M.1
Wadamoto, M.2
Chan, A.3
Scheidt, K.A.4
-
8
-
-
70349690230
-
Highly enantioselective intramolecular Michael reactions by d-camphor-derived triazolium salts
-
Li, Y.,Wang, X-Q., Zheng, C. & You, S-L. Highly enantioselective intramolecular Michael reactions by d-camphor-derived triazolium salts. Chem. Commun. 5823-5825 (2009).
-
(2009)
Chem. Commun.
, pp. 5823-5825
-
-
Li, Y.1
Wang, X.-Q.2
Zheng, C.3
You, S.-L.4
-
9
-
-
80052770020
-
Highly stereoselective synthesis of 1,2,3-trisubstituted indanes via oxidative N -heterocyclic carbenecatalyzed cascades
-
Biswas, A., Sarkar, S. D., Fröhlich, R. & Studer, A. Highly stereoselective synthesis of 1,2,3-trisubstituted indanes via oxidative N -heterocyclic carbenecatalyzed cascades. Org. Lett. 13, 4966-4969 (2011).
-
(2011)
Org. Lett.
, vol.13
, pp. 4966-4969
-
-
Biswas, A.1
Sarkar, S.D.2
Fröhlich, R.3
Studer, A.4
-
10
-
-
77957654050
-
Highly stereoselective synthesis of indanes with four stereogenic centers via sequential Michael reaction and [3+2] cycloaddition
-
Chua, P. J. et al. Highly stereoselective synthesis of indanes with four stereogenic centers via sequential Michael reaction and [3+2] cycloaddition. Chem. Commun. 46, 7611-7613 (2010).
-
(2010)
Chem. Commun.
, vol.46
, pp. 7611-7613
-
-
Chua, P.J.1
-
12
-
-
15844379072
-
5-Endo -trigonal reactions: A disfavoured ring closure
-
Baldwin, J. E. et al. 5-Endo -trigonal reactions: a disfavoured ring closure. J. Chem. Soc. Chem. Commun. 736-738 (1976).
-
(1976)
J. Chem. Soc. Chem. Commun.
, pp. 736-738
-
-
Baldwin, J.E.1
-
13
-
-
37049098529
-
Rules for ring closure. Stereoelectronic control in the endocyclic alkylation of ketone enolates
-
Baldwin, J. E. & Kruse, L. I. Rules for ring closure. Stereoelectronic control in the endocyclic alkylation of ketone enolates. J. Chem. Soc. Chem. Commun. 233-235 (1977).
-
(1977)
J. Chem. Soc. Chem. Commun.
, pp. 233-235
-
-
Baldwin, J.E.1
Kruse, L.I.2
-
14
-
-
84887444614
-
Finding the right path: Baldwin 'Rules for Ring Closure' and stereoelectronic control of cyclizations
-
Alabugin, I. V. & Gilmore, K. Finding the right path: Baldwin 'Rules for Ring Closure' and stereoelectronic control of cyclizations. Chem. Commun. 49, 11246-11250 (2013).
-
(2013)
Chem. Commun.
, vol.49
, pp. 11246-11250
-
-
Alabugin, I.V.1
Gilmore, K.2
-
16
-
-
33748788268
-
Studies of the generation and pericyclic behavior of cyclic pentadienyl carbanions. Alkylation reactions as an efficient route to functionalized cis-bicyclo[3.3.0] octenes
-
Williams, D. R., Reeves, J. T., Nag, P. P., Pitcock,W. H.Jr & Baik, M-H. Studies of the generation and pericyclic behavior of cyclic pentadienyl carbanions. Alkylation reactions as an efficient route to functionalized cis-bicyclo[3.3.0] octenes. J. Am. Chem. Soc. 128, 12339-12348 (2006).
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 12339-12348
-
-
Williams, D.R.1
Reeves, J.T.2
Nag, P.P.3
Pitcock, W.H.4
Baik, M.-H.5
-
17
-
-
72449134351
-
Catalytic asymmetric 6? Electrocyclization: Enantioselective synthesis of functionalized indolines
-
Maciver, E. E., Thompson, S. & Smith, M. D. Catalytic asymmetric 6? electrocyclization: enantioselective synthesis of functionalized indolines. Angew. Chem. Int. Ed. 48, 9979-9982 (2009).
-
(2009)
Angew. Chem. Int. Ed.
, vol.48
, pp. 9979-9982
-
-
Maciver, E.E.1
Thompson, S.2
Smith, M.D.3
-
18
-
-
84862908862
-
Catalytic enantioselective electrocyclic cascades
-
Maciver, E. E., Knipe, P. C., Cridland, A. P., Thompson, A. L. & Smith, M. D. Catalytic enantioselective electrocyclic cascades. Chem. Sci. 3, 537-540 (2012).
-
(2012)
Chem. Sci.
, vol.3
, pp. 537-540
-
-
Maciver, E.E.1
Knipe, P.C.2
Cridland, A.P.3
Thompson, A.L.4
Smith, M.D.5
-
19
-
-
84878792831
-
Cation-directed enantioselective synthesis of quaternary-substituted indolenines
-
Li, M.,Woods, P. A. & Smith, M. D. Cation-directed enantioselective synthesis of quaternary-substituted indolenines. Chem. Sci. 4, 2907-2911 (2013).
-
(2013)
Chem. Sci.
, vol.4
, pp. 2907-2911
-
-
Li, M.1
Woods, P.A.2
Smith, M.D.3
-
20
-
-
33744738548
-
A new modular indole synthesis. Construction of the highly strained CDEF parent tetracycle of Nodulisporic acids A and B
-
Smith, A. B. III, Kürti, L. & Davulcu, A. H. A new modular indole synthesis. Construction of the highly strained CDEF parent tetracycle of Nodulisporic acids A and B. Org. Lett. 8, 2167-2170 (2006).
-
(2006)
Org. Lett.
, vol.8
, pp. 2167-2170
-
-
Smith, A.B.1
Kürti, L.2
Davulcu, A.H.3
-
21
-
-
84876234339
-
Recent developments in asymmetric phase-transfer reactions
-
Shirakawa, S. & Maruoka, K. Recent developments in asymmetric phase-transfer reactions. Angew. Chem. Int. Ed. 52, 4312-4348 (2013).
-
(2013)
Angew. Chem. Int. Ed.
, vol.52
, pp. 4312-4348
-
-
Shirakawa, S.1
Maruoka, K.2
-
22
-
-
62349095651
-
Synthesis and evaluation of chiral dibenzazepinium halide phase-transfer catalysts
-
Lygo, B., Allbutt, B., Beaumont, D. J., Butt, U. & Gilks, J. A. R. Synthesis and evaluation of chiral dibenzazepinium halide phase-transfer catalysts. Synlett 675-680 (2009).
-
(2009)
Synlett
, pp. 675-680
-
-
Lygo, B.1
Allbutt, B.2
Beaumont, D.J.3
Butt, U.4
Gilks, J.A.R.5
-
23
-
-
16244410177
-
Powerful chiral phase-transfer catalysts for the asymmetric synthesis of α-alkyl- and α,α-dialkyl-α-amino acids
-
Kitamura, M., Shirakawa, S. & Maruoka, K. Powerful chiral phase-transfer catalysts for the asymmetric synthesis of α-alkyl- and α,α-dialkyl-α-amino acids. Angew. Chem. Int. Ed. 44, 1549-1551 (2005).
-
(2005)
Angew. Chem. Int. Ed.
, vol.44
, pp. 1549-1551
-
-
Kitamura, M.1
Shirakawa, S.2
Maruoka, K.3
-
24
-
-
0034738068
-
Practical catalytic enantioselective synthesis of α,α-dialkyl-α-amino acids by chiral phase-transfer catalysis
-
Ooi, T., Takeuchi, M., Kameda, M. & Maruoka, K. Practical catalytic enantioselective synthesis of α,α-dialkyl-α-amino acids by chiral phase-transfer catalysis. J. Am. Chem. Soc. 122, 5228-5229 (2000).
-
(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 5228-5229
-
-
Ooi, T.1
Takeuchi, M.2
Kameda, M.3
Maruoka, K.4
-
25
-
-
0037473547
-
Design of N-spiro C2-symmetric chiral quaternary ammonium bromides as novel chiral phase-transfer catalysts: Synthesis and application to practical asymmetric synthesis of α-amino acids
-
Ooi, T., Kameda, M. & Maruoka, K. Design of N-spiro C2-symmetric chiral quaternary ammonium bromides as novel chiral phase-transfer catalysts: synthesis and application to practical asymmetric synthesis of α-amino acids. J. Am. Chem. Soc. 125, 5139-5151(2003).
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 5139-5151
-
-
Ooi, T.1
Kameda, M.2
Maruoka, K.3
-
26
-
-
0038721888
-
A generic approach for the catalytic reduction of nitriles
-
Caddick, S., Judd, D. B., Lewis, A. K. de K., Reich, M. T. & Williams, M. R. V. A generic approach for the catalytic reduction of nitriles. Tetrahedron 59, 5417-5423 (2003).
-
(2003)
Tetrahedron
, vol.59
, pp. 5417-5423
-
-
Caddick, S.1
Judd, D.B.2
De Lewis, A.K.K.3
Reich, M.T.4
Williams, M.R.V.5
-
28
-
-
72449135778
-
A catalytic asymmetric 6π electrocyclization: Enantioselective synthesis of 2-pyrazolines
-
Müller, S. & List, B. A catalytic asymmetric 6π electrocyclization: enantioselective synthesis of 2-pyrazolines. Angew. Chem. Int. Ed. 48, 9975-9978 (2009).
-
(2009)
Angew. Chem. Int. Ed.
, vol.48
, pp. 9975-9978
-
-
Müller, S.1
List, B.2
-
29
-
-
84880837990
-
Asymmetric ion pair catalysis of 6π electrocyclizations: Brønsted acid catalyzed enantioselective synthesis of optically active 1,4-dihydropyridazines
-
Das, A., Volla, C. M. R., Atodiresei, I., Bettray, W. & Rueping, M. Asymmetric ion pair catalysis of 6π electrocyclizations: Brønsted acid catalyzed enantioselective synthesis of optically active 1,4-dihydropyridazines. Angew. Chem. Int. Ed. 52, 8008-8011 (2013).
-
(2013)
Angew. Chem. Int. Ed.
, vol.52
, pp. 8008-8011
-
-
Das, A.1
Volla, C.M.R.2
Atodiresei, I.3
Bettray, W.4
Rueping, M.5
-
30
-
-
54049095251
-
Catalysis of 6π electrocyclizations
-
Bishop, L. M., Barbarow, J. E., Bergman, R. G. & Trauner, D. Catalysis of 6π electrocyclizations. Angew. Chem. Int. Ed. 47, 8100-8103 (2008).
-
(2008)
Angew. Chem. Int. Ed.
, vol.47
, pp. 8100-8103
-
-
Bishop, L.M.1
Barbarow, J.E.2
Bergman, R.G.3
Trauner, D.4
-
31
-
-
2642695174
-
β' Metalation of α,β-unsaturated tertiary amides
-
Kempf, D. J., Wilson, K. D. & Beak, P. β' Metalation of α,β-unsaturated tertiary amides. J. Org. Chem. 47, 1610-1612 (1982).
-
(1982)
J. Org. Chem.
, vol.47
, pp. 1610-1612
-
-
Kempf, D.J.1
Wilson, K.D.2
Beak, P.3
-
32
-
-
0009594084
-
5-Endo-trigonal ring closures of unsaturated sulfones
-
Auvray, P., Knochel, P. & Normant, J. F. 5-Endo-trigonal ring closures of unsaturated sulfones. Tetrahedron Lett. 26, 4455-4458 (1985).
-
(1985)
Tetrahedron Lett.
, vol.26
, pp. 4455-4458
-
-
Auvray, P.1
Knochel, P.2
Normant, J.F.3
-
33
-
-
0005628635
-
[3+2] Cyclization -elimination route to cyclopentenyl sulfones using (phenylsulfonyl)-1,2-propadiene
-
Padwa, A. & Yeske, P. E. [3+2] Cyclization -elimination route to cyclopentenyl sulfones using (phenylsulfonyl)-1,2-propadiene. J. Org. Chem. 56, 6386-6390 (1991).
-
(1991)
J. Org. Chem.
, vol.56
, pp. 6386-6390
-
-
Padwa, A.1
Yeske, P.E.2
-
34
-
-
0142062462
-
β-Lactams or ã-lactams by 4-exo-trig or 5-endo-trig anionic cyclisation of lithiated acrylamide derivatives
-
Clayden, J., Watson, D. W., Helliwell, M. & Chambers, M. β-Lactams or ã-lactams by 4-exo-trig or 5-endo-trig anionic cyclisation of lithiated acrylamide derivatives. Chem. Commun. 2582-2583 (2003).
-
(2003)
Chem. Commun.
, pp. 2582-2583
-
-
Clayden, J.1
Watson, D.W.2
Helliwell, M.3
Chambers, M.4
-
35
-
-
2442454610
-
Formation of 3-pyrrolin-2-ones via 5-endo-trig cyclization
-
Asaoka, M. et al. Formation of 3-pyrrolin-2-ones via 5-endo-trig cyclization. Heterocycles 63, 1009-1012 (2004).
-
(2004)
Heterocycles
, vol.63
, pp. 1009-1012
-
-
Asaoka, M.1
-
36
-
-
0036012052
-
The 5-endo-trig cyclization of gemdifluoroolefins with sp3 carbon nucleophiles: Synthesis of 1-fluorocyclopentenes
-
Ichikawa, J., Sakoda, K. & Wada, Y. The 5-endo-trig cyclization of gemdifluoroolefins with sp3 carbon nucleophiles: synthesis of 1-fluorocyclopentenes. Chem. Lett. 31, 282-283 (2002)
-
(2002)
Chem. Lett.
, vol.31
, pp. 282-283
-
-
Ichikawa, J.1
Sakoda, K.2
Wada, Y.3
-
37
-
-
77955658256
-
Diastereoselective synthesis of substituted prolines via 5-endo-trig cyclisations of aza-[2,3]-Wittig sigmatropic rearrangement products
-
Anderson, J. C. & Davies, E. A. Diastereoselective synthesis of substituted prolines via 5-endo-trig cyclisations of aza-[2,3]-Wittig sigmatropic rearrangement products. Tetrahedron 66, 6300-6308 (2010).
-
(2010)
Tetrahedron
, vol.66
, pp. 6300-6308
-
-
Anderson, J.C.1
Davies, E.A.2
-
38
-
-
78651350090
-
Synthetic scope, computational chemistry and mechanism of a base induced 5-endo cyclization of benzyl alkynyl sulfides
-
Motto, J. M. et al. Synthetic scope, computational chemistry and mechanism of a base induced 5-endo cyclization of benzyl alkynyl sulfides. Tetrahedron 67, 1002-1010 (2011).
-
(2011)
Tetrahedron
, vol.67
, pp. 1002-1010
-
-
Motto, J.M.1
-
39
-
-
10844270846
-
Asymmetric induction in the basecatalysed Michael addition of nitromethane to chalcone
-
Colonna, S., Hiemstra, H. & Wynberg, H. Asymmetric induction in the basecatalysed Michael addition of nitromethane to chalcone. J. Chem. Soc. Chem. Commun. 238-239 (1978).
-
(1978)
J. Chem. Soc. Chem. Commun.
, pp. 238-239
-
-
Colonna, S.1
Hiemstra, H.2
Wynberg, H.3
-
40
-
-
0000867232
-
Chiral Michael addition: Methyl vinyl ketone addition catalyzed by Cinchona alkaloid derivatives
-
Conn, R. S. E., Lovell, A. V., Karady, S. & Weinstock, L. M. Chiral Michael addition: methyl vinyl ketone addition catalyzed by Cinchona alkaloid derivatives. J. Org. Chem. 51, 4710-4711 (1986).
-
(1986)
J. Org. Chem.
, vol.51
, pp. 4710-4711
-
-
Conn, R.S.E.1
Lovell, A.V.2
Karady, S.3
Weinstock, L.M.4
-
41
-
-
4644273111
-
Highly enantioselective conjugate addition of nitroalkanes to alkylidenemalonates using efficient phase-transfer catalysis of Nspiro chiral ammonium bromides
-
Ooi, T., Fujioka, S. & Maruoka, K. Highly enantioselective conjugate addition of nitroalkanes to alkylidenemalonates using efficient phase-transfer catalysis of Nspiro chiral ammonium bromides. J. Am. Chem. Soc. 126, 11790-11791 (2004).
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 11790-11791
-
-
Ooi, T.1
Fujioka, S.2
Maruoka, K.3
-
42
-
-
19544379484
-
Asymmetric Michael addition of glycine imines via quaternary ammonium ion catalysis
-
Lygo, B., Allbutt, B. & Kirton, E. H. M. Asymmetric Michael addition of glycine imines via quaternary ammonium ion catalysis. Tetrahedron Lett. 46, 4461-4464 (2005).
-
(2005)
Tetrahedron Lett.
, vol.46
, pp. 4461-4464
-
-
Lygo, B.1
Allbutt, B.2
Kirton, E.H.M.3
-
43
-
-
24744453294
-
Thermodynamic and strain effects in the competition between 5-exo-dig and 6-endo-dig cyclizations of vinyl and aryl radicals
-
Alabugin, I. V. & Manoharan, M. Thermodynamic and strain effects in the competition between 5-exo-dig and 6-endo-dig cyclizations of vinyl and aryl radicals. J. Am. Chem. Soc. 127, 12583-12954 (2005).
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 12583-12954
-
-
Alabugin, I.V.1
Manoharan, M.2
-
44
-
-
79960014189
-
Farewell to the HSAB treatment of ambident reactivity
-
Mayr, H., Breugst, M. & Ofial, A. R. Farewell to the HSAB treatment of ambident reactivity. Angew. Chem. Int. Ed. 50, 6470 (2011).
-
(2011)
Angew. Chem. Int. Ed.
, vol.50
, pp. 6470
-
-
Mayr, H.1
Breugst, M.2
Ofial, A.R.3
-
45
-
-
77954855923
-
Marcus analysis of ambident reactivity
-
Breugst, M., Zipse, H., Guthrie, J. P. & Mayr, H. Marcus analysis of ambident reactivity. Angew. Chem. Int. Ed. 49, 5165-5169 (2010).
-
(2010)
Angew. Chem. Int. Ed.
, vol.49
, pp. 5165-5169
-
-
Breugst, M.1
Zipse, H.2
Guthrie, J.P.3
Mayr, H.4
-
46
-
-
80051586211
-
Rules for anionic and radical ring closure of alkynes
-
Alabugin, I. V., Gilmore, K. & Manoharan, M. Rules for anionic and radical ring closure of alkynes. J. Am. Chem. Soc. 133, 12608-12623 (2011).
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 12608-12623
-
-
Alabugin, I.V.1
Gilmore, K.2
Manoharan, M.3
-
47
-
-
21744442964
-
5-Endo-dig radical cyclizations: 'The poor cousins' of the radical cyclizations family
-
Alabugin, I. V. & Manoharan, M. 5-Endo-dig radical cyclizations: 'the poor cousins' of the radical cyclizations family. J. Am. Chem. Soc. 127, 9534-9545 (2005).
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 9534-9545
-
-
Alabugin, I.V.1
Manoharan, M.2
-
48
-
-
0000535805
-
An extraordinarily facile sulfoxide automerization
-
Ross, J. A., Seiders, R. P. & Lemal, D. M. An extraordinarily facile sulfoxide automerization. J. Am. Chem. Soc. 98, 4325-4327 (1976).
-
(1976)
J. Am. Chem. Soc.
, vol.98
, pp. 4325-4327
-
-
Ross, J.A.1
Seiders, R.P.2
Lemal, D.M.3
-
49
-
-
2842584372
-
1,5,-Electrocyclizations -an important principle of heterocyclic chemistry
-
Huisgen, R. 1,5,-Electrocyclizations -an important principle of heterocyclic chemistry. Angew. Chem. Int. Ed. 19, 947-973 (1980).
-
(1980)
Angew. Chem. Int. Ed.
, vol.19
, pp. 947-973
-
-
Huisgen, R.1
-
50
-
-
84863493125
-
Aromatic transition states in nonpericyclic reactions: Anionic 5-endo cyclizations are aborted sigmatropic shifts
-
Gilmore, K., Manoharan, M., Wu, J. I., Schleyer, P. v. R. & Alabugin, I. V. Aromatic transition states in nonpericyclic reactions: anionic 5-endo cyclizations are aborted sigmatropic shifts. J. Am. Chem. Soc. 134, 10584-10594 (2012).
-
(2012)
J. Am. Chem. Soc.
, vol.134
, pp. 10584-10594
-
-
Gilmore, K.1
Manoharan, M.2
Wu, J.I.3
Schleyer, P.V.R.4
Alabugin, I.V.5
-
51
-
-
80051586277
-
Cyclizations of alkynes: Revisiting Baldwin's rules for ring closure
-
Alabugin, I. V. & Gilmore, K. Cyclizations of alkynes: revisiting Baldwin's rules for ring closure. Chem. Rev. 111, 6513-6556 (2011).
-
(2011)
Chem. Rev.
, vol.111
, pp. 6513-6556
-
-
Alabugin, I.V.1
Gilmore, K.2
-
52
-
-
0030896847
-
On the minimum requirements for chiral recognition
-
Pirkle, W. H. On the minimum requirements for chiral recognition. Chirality 9, 103 (1997).
-
(1997)
Chirality
, vol.9
, pp. 103
-
-
Pirkle, W.H.1
-
53
-
-
85021596191
-
Tetrabutylammonium salts of CH-acidic carbonyl compounds: Real carbanions or supramolecules?
-
Reetz, M. T., Hütte, S. & Goddard, R. Tetrabutylammonium salts of CH-acidic carbonyl compounds: real carbanions or supramolecules? J. Am. Chem. Soc. 115, 9339-9340 (1993).
-
(1993)
J. Am. Chem. Soc.
, vol.115
, pp. 9339-9340
-
-
Reetz, M.T.1
Hütte, S.2
Goddard, R.3
-
55
-
-
84885677452
-
Ion-pairing of phosphonium salts in solution: C-H···Halogen and C-H···π hydrogen bonds
-
Ammer, J. et al. Ion-pairing of phosphonium salts in solution: C-H···Halogen and C-H···π hydrogen bonds. Chem. Eur. J. 19, 14612-14630 (2013).
-
(2013)
Chem. Eur. J.
, vol.19
, pp. 14612-14630
-
-
Ammer, J.1
|