-
1
-
-
78649265601
-
-
For selected reviews, see
-
For selected reviews, see
-
-
-
-
2
-
-
39149102146
-
-
I. Larrosa, P. Romea, F. Urpí, Tetrahedron 2008, 64, 2683
-
(2008)
Tetrahedron
, vol.64
, pp. 2683
-
-
Larrosa, I.1
Romea, P.2
Urpí, F.3
-
3
-
-
62349138270
-
-
in (Eds.: G. W. Gribble, J. A. Joule), Elsevier, Oxford
-
J. B. Bremner, S. Samosorn, in Progress in Heterocyclic Chemistry, Vol. 18 (Eds.:, G. W. Gribble, J. A. Joule,), Elsevier, Oxford, 2007, pp. 402 - 429
-
(2007)
Progress in Heterocyclic Chemistry, Vol. 18
, pp. 402-429
-
-
Bremner, J.B.1
Samosorn, S.2
-
4
-
-
62349083727
-
-
in (Eds.: G. W. Gribble, J. A. Joule), Elsevier, Oxford
-
G. R. Newkome, in Progress in Heterocyclic Chemistry, Vol. 18 (Eds.:, G. W. Gribble, J. A. Joule,), Elsevier, Oxford, 2007, pp. 430 - 448
-
(2007)
Progress in Heterocyclic Chemistry, Vol. 18
, pp. 430-448
-
-
Newkome, G.R.1
-
6
-
-
33747890433
-
-
N. L. Snyder, H. M. Haines, M. W. Peczuh, Tetrahedron 2006, 62, 9301
-
(2006)
Tetrahedron
, vol.62
, pp. 9301
-
-
Snyder, N.L.1
Haines, H.M.2
Peczuh, M.W.3
-
8
-
-
33846930947
-
-
J. W. Blunt, B. R. Copp, W.-P. Hu, M. H. G. Munro, P. T. Northcote, M. R. Prinsep, Nat. Prod. Rep. 2007, 24, 31
-
(2007)
Nat. Prod. Rep.
, vol.24
, pp. 31
-
-
Blunt, J.W.1
Copp, B.R.2
Hu, W.-P.3
Munro, M.H.G.4
Northcote, P.T.5
Prinsep, M.R.6
-
9
-
-
29244452570
-
-
M. Saleem, H. J. Kim, M. S. Ali, Y. S. Lee, Nat. Prod. Rep. 2005, 22, 696
-
(2005)
Nat. Prod. Rep.
, vol.22
, pp. 696
-
-
Saleem, M.1
Kim, H.J.2
Ali, M.S.3
Lee, Y.S.4
-
12
-
-
78649231583
-
-
For reviews and overviews, see
-
For reviews and overviews, see
-
-
-
-
13
-
-
61849124839
-
-
M. Brasholz, H.-U. Reissig, R. Zimmer, Acc. Chem. Res. 2009, 42, 45
-
(2009)
Acc. Chem. Res.
, vol.42
, pp. 45
-
-
Brasholz, M.1
Reissig, H.-U.2
Zimmer, R.3
-
18
-
-
22944485617
-
-
S. Ma, Chem. Rev. 2005, 105, 2829
-
(2005)
Chem. Rev.
, vol.105
, pp. 2829
-
-
Ma, S.1
-
20
-
-
4544320494
-
-
(Eds.: N. Krause, A. S. K. Hashmi), Wiley-VCH, Weinheim
-
Modern Allene Chemistry (Eds.:, N. Krause, A. S. K. Hashmi,), Wiley-VCH, Weinheim, 2004
-
(2004)
Modern Allene Chemistry
-
-
-
26
-
-
0034245863
-
-
R. Zimmer, C. U. Dinesh, E. Nandanan, F. A. Khan, Chem. Rev. 2000, 100, 3067.
-
(2000)
Chem. Rev.
, vol.100
, pp. 3067
-
-
Zimmer, R.1
Dinesh, C.U.2
Nandanan, E.3
Khan, F.A.4
-
27
-
-
78649243659
-
-
For the Au-catalyzed 5-endo cycloisomerization of an α,α'- allendiol to give a dihydrofuran, see
-
For the Au-catalyzed 5-endo cycloisomerization of an α,α'- allendiol to give a dihydrofuran, see
-
-
-
-
28
-
-
34848927802
-
-
C. Deutsch, B. H. Lipshutz, N. Krause, Angew. Chem. 2007, 119, 1677
-
(2007)
Angew. Chem.
, vol.119
, pp. 1677
-
-
Deutsch, C.1
Lipshutz, B.H.2
Krause, N.3
-
29
-
-
34248146411
-
-
for the Au-catalyzed 5-endo cycloisomerization of α,β- allendiols to give dihydrofurans, see
-
Angew. Chem. Int. Ed. 2007, 46, 1650; for the Au-catalyzed 5-endo cycloisomerization of α,β-allendiols to give dihydrofurans, see
-
(2007)
Angew. Chem. Int. Ed.
, vol.46
, pp. 1650
-
-
-
31
-
-
73349115986
-
-
Z. Gao, Y. Li, J. P. Cooksey, T. N. Snaddon, S. Schunk, E. M. E. Viseux, S. M. McAteer, P. J. Kocienski, Angew. Chem. 2009, 121, 5122
-
(2009)
Angew. Chem.
, vol.121
, pp. 5122
-
-
Gao, Z.1
Li, Y.2
Cooksey, J.P.3
Snaddon, T.N.4
Schunk, S.5
Viseux, E.M.E.6
McAteer, S.M.7
Kocienski, P.J.8
-
32
-
-
70349909728
-
-
for the Au-catalyzed 5-endo cycloisomerization of N-hydroxy-α- aminoallenes to give N-hydroxypyrrolines, see
-
Angew. Chem. Int. Ed. 2009, 48, 5022; for the Au-catalyzed 5-endo cycloisomerization of N-hydroxy-α-aminoallenes to give N-hydroxypyrrolines, see
-
(2009)
Angew. Chem. Int. Ed.
, vol.48
, pp. 5022
-
-
-
35
-
-
78649286216
-
-
Depending on the regioselectivity (endo-trig versus endo-dig versus exo-dig versus exo-trig cyclization) and chemoselectivity (distal versus proximal nucleophile cyclization) either of the eight possible heterocycles could be the reaction products
-
Depending on the regioselectivity (endo-trig versus endo-dig versus exo-dig versus exo-trig cyclization) and chemoselectivity (distal versus proximal nucleophile cyclization) either of the eight possible heterocycles could be the reaction products.
-
-
-
-
36
-
-
78649310878
-
-
See, for example
-
See, for example
-
-
-
-
37
-
-
77952725353
-
-
B. Alcaide, P. Almendros, R. Carrascosa, M. R. Torres, Adv. Synth. Catal. 2010, 352, 1277
-
(2010)
Adv. Synth. Catal.
, vol.352
, pp. 1277
-
-
Alcaide, B.1
Almendros, P.2
Carrascosa, R.3
Torres, M.R.4
-
38
-
-
77949860743
-
-
B. Alcaide, P. Almendros, A. Luna, M. R. Torres, Adv. Synth. Catal. 2010, 352, 621
-
(2010)
Adv. Synth. Catal.
, vol.352
, pp. 621
-
-
Alcaide, B.1
Almendros, P.2
Luna, A.3
Torres, M.R.4
-
39
-
-
63749122772
-
-
B. Alcaide, P. Almendros, T. Martínez del Campo, M. T. Quirós, Chem. Eur. J. 2009, 15, 3344
-
(2009)
Chem. Eur. J.
, vol.15
, pp. 3344
-
-
Alcaide, B.1
Almendros, P.2
Martínez Del Campo, T.3
Quirós, M.T.4
-
40
-
-
60749096548
-
-
B. Alcaide, P. Almendros, T. Martínez del Campo, E. Soriano, J. L. Marco-Contelles, Chem. Eur. J. 2009, 15, 1901
-
(2009)
Chem. Eur. J.
, vol.15
, pp. 1901
-
-
Alcaide, B.1
Almendros, P.2
Martínez Del Campo, T.3
Soriano, E.4
Marco-Contelles, J.L.5
-
41
-
-
38149116921
-
-
B. Alcaide, P. Almendros, R. Carrascosa, M. C. Redondo, Chem. Eur. J. 2008, 14, 637
-
(2008)
Chem. Eur. J.
, vol.14
, pp. 637
-
-
Alcaide, B.1
Almendros, P.2
Carrascosa, R.3
Redondo, M.C.4
-
42
-
-
53649110016
-
-
B. Alcaide, P. Almendros, T. Martínez del Campo, Angew. Chem. 2007, 119, 6804
-
(2007)
Angew. Chem.
, vol.119
, pp. 6804
-
-
Alcaide, B.1
Almendros, P.2
Martínez Del Campo, T.3
-
44
-
-
53849128160
-
-
Angew. Chem. 2007, 119, 6804
-
(2007)
Angew. Chem.
, vol.119
, pp. 6804
-
-
-
45
-
-
34547214986
-
-
B. Alcaide, P. Almendros, T. Martínez del Campo, Angew. Chem. 2006, 118, 4613
-
(2006)
Angew. Chem.
, vol.118
, pp. 4613
-
-
Alcaide, B.1
Almendros, P.2
Martínez Del Campo, T.3
-
47
-
-
62349125016
-
-
For a preliminary report on part of this study, see
-
For a preliminary report on part of this study, see:, B. Alcaide, P. Almendros, R. Carrascosa, T. Martínez del Campo, Chem. Eur. J. 2009, 15, 2496.
-
(2009)
Chem. Eur. J.
, vol.15
, pp. 2496
-
-
Alcaide, B.1
Almendros, P.2
Carrascosa, R.3
Martínez Del Campo, T.4
-
49
-
-
0000772702
-
-
A. Dondoni, G. Fantin, M. Fogagnolo, A. Medici, P. Pedrini, J. Org. Chem. 1989, 54, 693.
-
(1989)
J. Org. Chem.
, vol.54
, pp. 693
-
-
Dondoni, A.1
Fantin, G.2
Fogagnolo, M.3
Medici, A.4
Pedrini, P.5
-
50
-
-
33845376028
-
-
B. M. Trost, J. L. Belletire, S. Godleski, P. G. McDougal, J. M. Balkovec, J. J. Baldwin, M. E. Christy, G. S. Ponticello, S. L. Varga, J. P. Springer, J. Org. Chem. 1986, 51, 2370
-
(1986)
J. Org. Chem.
, vol.51
, pp. 2370
-
-
Trost, B.M.1
Belletire, J.L.2
Godleski, S.3
McDougal, P.G.4
Balkovec, J.M.5
Baldwin, J.J.6
Christy, M.E.7
Ponticello, G.S.8
Varga, S.L.9
Springer, J.P.10
-
51
-
-
7444256242
-
-
for a review, see
-
K. M. Sureshan, T. Miyasou, S. Miyamori, Y. Watanabe, Tetrahedron: Asymmetry 2004, 15, 3357; for a review, see
-
(2004)
Tetrahedron: Asymmetry
, vol.15
, pp. 3357
-
-
Sureshan, K.M.1
Miyasou, T.2
Miyamori, S.3
Watanabe, Y.4
-
52
-
-
0942277395
-
-
J. M. Seco, E. Quiñoá, R. Riguera, Chem. Rev. 2004, 104, 17.
-
(2004)
Chem. Rev.
, vol.104
, pp. 17
-
-
Seco, J.M.1
Quiñoá, E.2
Riguera, R.3
-
53
-
-
78649305106
-
-
For selected reviews on gold catalysis, see
-
For selected reviews on gold catalysis, see
-
-
-
-
54
-
-
78649310436
-
-
Chem. Rev. 2008, 108, Issue 8, Eds. B. Lipshutz, Y. Yamamoto
-
Chem. Rev. 2008, 108, Issue 8, Eds. B. Lipshutz, Y. Yamamoto
-
-
-
-
55
-
-
78649247910
-
-
Chem. Soc. Rev. 2008, 37, Issue 9, Eds. G. J. Hutchings, M. Brust, H. Schmidbaur
-
Chem. Soc. Rev. 2008, 37, Issue 9, Eds. G. J. Hutchings, M. Brust, H. Schmidbaur
-
-
-
-
63
-
-
33845247117
-
-
for reviews on platinum catalysis, see
-
L. Zhang, J. Sun, S. A. Kozmin, Adv. Synth. Catal. 2006, 348, 2271; for reviews on platinum catalysis, see
-
(2006)
Adv. Synth. Catal.
, vol.348
, pp. 2271
-
-
Zhang, L.1
Sun, J.2
Kozmin, S.A.3
-
64
-
-
38349163202
-
-
A. R. Chianese, S. J. Lee, M. R. Gagné, Angew. Chem. 2007, 119, 4118
-
(2007)
Angew. Chem.
, vol.119
, pp. 4118
-
-
Chianese, A.R.1
Lee, S.J.2
Gagné, M.R.3
-
66
-
-
34548299812
-
-
for overviews on Au- and Pt- catalyzed reactions, see
-
C. Liu, C. F. Bender, X. Han, R. A. Widenhoefer, Chem. Commun. 2007, 3607; for overviews on Au- and Pt- catalyzed reactions, see
-
(2007)
Chem. Commun.
, pp. 3607
-
-
Liu, C.1
Bender, C.F.2
Han, X.3
Widenhoefer, R.A.4
-
69
-
-
78649315107
-
-
1H resonances by 2D NMR spectroscopic studies (COSY, HSQC, HMBC), the stereochemistry of the new quaternary stereocenter was unequivocally determined by a series of selective 1D gradient-enhanced NOE interaction experiments (ge-1D NOESY)
-
1H resonances by 2D NMR spectroscopic studies (COSY, HSQC, HMBC), the stereochemistry of the new quaternary stereocenter was unequivocally determined by a series of selective 1D gradient-enhanced NOE interaction experiments (ge-1D NOESY).
-
-
-
-
70
-
-
78649233347
-
-
The formation of quaternary centers in an asymmetric manner possesses a particular challenge for organic synthesis because of steric repulsion between the carbon substituents in the product and the difficulty in achieving good stereocontrol; for recent selected reviews, see
-
The formation of quaternary centers in an asymmetric manner possesses a particular challenge for organic synthesis because of steric repulsion between the carbon substituents in the product and the difficulty in achieving good stereocontrol; for recent selected reviews, see
-
-
-
-
75
-
-
32644439884
-
-
the total diastereoselectivity for tetrahydrofurans 5 could be explained by attack of the hydroxy group at the allenyl-metal complex from the less-hindered face
-
B. M. Trost, C. H. Jiang, Synthesis 2006, 369; the total diastereoselectivity for tetrahydrofurans 5 could be explained by attack of the hydroxy group at the allenyl-metal complex from the less-hindered face.
-
(2006)
Synthesis
, pp. 369
-
-
Trost, B.M.1
Jiang, C.H.2
-
76
-
-
78649299516
-
-
For the sole report on the hydroalkoxylation of γ-allenols catalyzed by platinum salts, see
-
For the sole report on the hydroalkoxylation of γ-allenols catalyzed by platinum salts, see
-
-
-
-
77
-
-
33746048429
-
-
4-catalyzed reaction of indoles with β-allenols to afford indole derivatives containing a six-membered ether ring at the 3-position, see
-
4-catalyzed reaction of indoles with β-allenols to afford indole derivatives containing a six-membered ether ring at the 3-position, see
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 9066
-
-
Zhang, Z.1
Liu, C.2
Kinder, R.E.3
Han, X.4
Qian, H.5
Widenhoefer, R.A.6
-
78
-
-
64049110343
-
-
W. Kong, J. Cui, Y. Yu, G. Chen, C. Fu, S. Ma, Org. Lett. 2009, 11, 1213.
-
(2009)
Org. Lett.
, vol.11
, pp. 1213
-
-
Kong, W.1
Cui, J.2
Yu, Y.3
Chen, G.4
Fu, C.5
Ma, S.6
-
79
-
-
78649271841
-
-
The development of new oxidation processes that employ transition-metal catalysis is a very important goal; for reviews, see
-
The development of new oxidation processes that employ transition-metal catalysis is a very important goal; for reviews, see
-
-
-
-
83
-
-
70549093538
-
-
H. Miyamura, M. Shiramizu, R. Matsubara, S. Kobayashi, Angew. Chem. 2008, 120, 8213
-
(2008)
Angew. Chem.
, vol.120
, pp. 8213
-
-
Miyamura, H.1
Shiramizu, M.2
Matsubara, R.3
Kobayashi, S.4
-
85
-
-
34250881661
-
-
X. Yu, S. Seo, T. J. Marks, J. Am. Chem. Soc. 2007, 129, 7244.
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 7244
-
-
Yu, X.1
Seo, S.2
Marks, T.J.3
-
86
-
-
0034638407
-
-
For Pd-catalyzed 5-exo and 6-exo haloetherifications, see
-
For Pd-catalyzed 5-exo and 6-exo haloetherifications, see:, C. Jonasson, A. Horváth, J.-E. Båckvall, J. Am. Chem. Soc. 2000, 122, 9600.
-
(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 9600
-
-
Jonasson, C.1
Horváth, A.2
Båckvall, J.-E.3
-
87
-
-
78649240934
-
-
Experimental procedures and full spectroscopic and analytical data for compounds not included in the Experimental Section are described in the Supporting Information; the characterization data and experimental procedures for 3 a - d, 4 aM, 4 am, 5 a, 5 b, 6 a - d, 7 aM, (R)-acetylmandelate derivate of 7 aM, (S)-acetylmandelate derivative of 7 aM, 7 am, 7 b, 8 aM, and 8 am and the NMR spectra of all the new compounds are given
-
Experimental procedures and full spectroscopic and analytical data for compounds not included in the Experimental Section are described in the Supporting Information; the characterization data and experimental procedures for 3 a - d, 4 aM, 4 am, 5 a, 5 b, 6 a - d, 7 aM, (R)-acetylmandelate derivate of 7 aM, (S)-acetylmandelate derivative of 7 aM, 7 am, 7 b, 8 aM, and 8 am and the NMR spectra of all the new compounds are given.
-
-
-
|