-
1
-
-
33845238277
-
-
For selected reviews, see: a
-
For selected reviews, see: a) J. P. Wolfe, M. B. Hay, Tetrahedron 2007, 63, 261;
-
(2007)
Tetrahedron
, vol.63
, pp. 261
-
-
Wolfe, J.P.1
Hay, M.B.2
-
2
-
-
33747890433
-
-
b) 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
-
3
-
-
33746294594
-
-
Eds, G. W. Gribble, J. A. Joule, Elsevier, Oxford
-
c) X.-L. Hou, Z. Yang, K.-S. Yeung, H. N. C. Wong in Progress in Heterocyclic Chemistry, Vol. 17 (Eds.: G. W. Gribble, J. A. Joule), Elsevier, Oxford, 2005, pp. 142-171;
-
(2005)
Progress in Heterocyclic Chemistry
, vol.17
, pp. 142-171
-
-
Hou, X.-L.1
Yang, Z.2
Yeung, K.-S.3
Wong, H.N.C.4
-
4
-
-
33746282995
-
-
Eds, G. W. Gribble, J. A. Joule, Elsevier, Oxford
-
d) X.-L. Hou, Z. Yang, K.-S. Yeung, H. N. C. Wong in Progress in Heterocyclic Chemistry, Vol. 16 (Eds.: G. W. Gribble, J. A. Joule), Elsevier, Oxford, 2004, pp. 156-197;
-
(2004)
Progress in Heterocyclic Chemistry
, vol.16
, pp. 156-197
-
-
Hou, X.-L.1
Yang, Z.2
Yeung, K.-S.3
Wong, H.N.C.4
-
5
-
-
1942472372
-
-
Eds, T. Eicher, J. S. Hauptmann, Wiley-VCH, Weinheim
-
e) The Chemistry of Heterocycles: Structure, Reactions, Syntheses, and Applications (Eds.: T. Eicher, J. S. Hauptmann), Wiley-VCH, Weinheim, 2003;
-
(2003)
The Chemistry of Heterocycles: Structure, Reactions, Syntheses, and Applications
-
-
-
6
-
-
0037017756
-
-
Special issue: Tetrahedron 2002, 58, 1779-2040;
-
f) Special issue: Tetrahedron 2002, 58, 1779-2040;
-
-
-
-
8
-
-
0002886647
-
-
Ed, C. W. Bird, Elsevier
-
h) H. Heaney, J. S. Ahn in Comprehensive Heterocyclic Chemistry II, Vol.2 (Ed.: C. W. Bird), Elsevier, 1995, pp. 297-350;
-
(1995)
Comprehensive Heterocyclic Chemistry II
, vol.2
, pp. 297-350
-
-
Heaney, H.1
Ahn, J.S.2
-
13
-
-
77957077490
-
-
Ed, A. R. Katritzky, Academic Press, New York
-
m) F. M. Dean in Advances in Heterocyclic Chemistry, Vol. 30 (Ed.: A. R. Katritzky), Academic Press, New York, 1982, pp. 167-238.
-
(1982)
Advances in Heterocyclic Chemistry
, vol.30
, pp. 167-238
-
-
Dean, F.M.1
-
14
-
-
22944485617
-
-
For general and comprehensive reviews, see: a
-
For general and comprehensive reviews, see: a) S. Ma, Chem. Rev. 2005, 105, 2829;
-
(2005)
Chem. Rev
, vol.105
, pp. 2829
-
-
Ma, S.1
-
15
-
-
4544320494
-
-
Eds, N. Krause, A. S. K. Hashmi, Wiley-VCH, Weinheim
-
b) Modern Allene Chemistry (Eds.: N. Krause, A. S. K. Hashmi), Wiley-VCH, Weinheim, 2004;
-
(2004)
Modern Allene Chemistry
-
-
-
16
-
-
0034245863
-
-
c) 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
-
22
-
-
0034675566
-
-
Angew. Chem. Int. Ed. 2000, 39, 3590.
-
(2000)
Chem. Int. Ed
, vol.39
, pp. 3590
-
-
Angew1
-
23
-
-
34547173252
-
-
See, for instance: a
-
See, for instance: a) B. Alcaide, P. Almendros, T. Martínez del Campo, R. Rodríguez-Acebes, Adv. Synth. Catal. 2007, 349, 749;
-
(2007)
Adv. Synth. Catal
, vol.349
, pp. 749
-
-
Alcaide, B.1
Almendros, P.2
Martínez del Campo, T.3
Rodríguez-Acebes, R.4
-
24
-
-
33847649540
-
-
b) B. Alcaide, P. Almendros, C. Aragoncillo, M. C. Redondo, J. Org. Chem. 2007, 72, 1604;
-
(2007)
J. Org. Chem
, vol.72
, pp. 1604
-
-
Alcaide, B.1
Almendros, P.2
Aragoncillo, C.3
Redondo, M.C.4
-
25
-
-
34547214986
-
-
c) B. Alcaide, P. Almendros, T. Martinez del Campo, Angew. Chem. 2006, 118, 4613;
-
(2006)
Angew. Chem
, vol.118
, pp. 4613
-
-
Alcaide, B.1
Almendros, P.2
Martinez del Campo, T.3
-
26
-
-
33746294191
-
-
Angew. Chem. Int. Ed. 2006, 45, 4501;
-
(2006)
Chem. Int. Ed
, vol.45
, pp. 4501
-
-
Angew1
-
27
-
-
33645307693
-
-
d) B. Alcaide, P. Almendros, J. M. Alonso, Chem. Eur. J. 2006, 12, 2874;
-
(2006)
Chem. Eur. J
, vol.12
, pp. 2874
-
-
Alcaide, B.1
Almendros, P.2
Alonso, J.M.3
-
29
-
-
32044451039
-
-
f) B. Alcaide, P. Almendros, C. Aragoncillo, M. C. Redondo, M. R. Torres, Chem. Eur. J. 2006, 12, 1539.
-
(2006)
Chem. Eur. J
, vol.12
, pp. 1539
-
-
Alcaide, B.1
Almendros, P.2
Aragoncillo, C.3
Redondo, M.C.4
Torres, M.R.5
-
30
-
-
11844305031
-
-
a) B. Alcaide, P. Almendros, C. Aragoncillo, M. C. Redondo, Eur. J. Org. Chem. 2005, 98;
-
(2005)
Eur. J. Org. Chem
, pp. 98
-
-
Alcaide, B.1
Almendros, P.2
Aragoncillo, C.3
Redondo, M.C.4
-
31
-
-
0037006835
-
-
b) B. Alcaide, P. Almendros, C. Aragoncillo, Chem. Eur. J. 2002, 8, 1719.
-
(2002)
Chem. Eur. J
, vol.8
, pp. 1719
-
-
Alcaide, B.1
Almendros, P.2
Aragoncillo, C.3
-
32
-
-
33746048429
-
-
The only available Pt-mediated oxycyclization of a γ-allenol is the 6-exo cyclization of 2,2-diphenylhexa-4,5-dien-1-ol, which leads to 6-methyl-3,3-diphenyl-3,4-dihydro-2H-pyran. See: Z. Zhang, C. Liu, R. E. Kinder, X. Han, H. Qian, R. A. Widenhoefer, J. Chem. Soc. 2006, 128, 9066.
-
The only available Pt-mediated oxycyclization of a γ-allenol is the 6-exo cyclization of 2,2-diphenylhexa-4,5-dien-1-ol, which leads to 6-methyl-3,3-diphenyl-3,4-dihydro-2H-pyran. See: Z. Zhang, C. Liu, R. E. Kinder, X. Han, H. Qian, R. A. Widenhoefer, J. Chem. Soc. 2006, 128, 9066.
-
-
-
-
33
-
-
0000383973
-
-
For selected examples of Ag-mediated heterocyclizations of α-allenols, see: a
-
For selected examples of Ag-mediated heterocyclizations of α-allenols, see: a) J. A. Marshall, R. H. Yu, J. F. Perkins, J. Org. Chem. 1995, 60, 5550;
-
(1995)
J. Org. Chem
, vol.60
, pp. 5550
-
-
Marshall, J.A.1
Yu, R.H.2
Perkins, J.F.3
-
35
-
-
33645064286
-
-
c) B. Alcaide, P. Almendros, R. Rodríguez-Acebes, J. Org. Chem. 2006, 71, 2346.
-
(2006)
J. Org. Chem
, vol.71
, pp. 2346
-
-
Alcaide, B.1
Almendros, P.2
Rodríguez-Acebes, R.3
-
36
-
-
34248637761
-
-
For a review of gold catalysis, see: a
-
For a review of gold catalysis, see: a) A. S. K. Hashmi, G. J. Hutchings, Angew. Chem. 2006, 118, 8064;
-
(2006)
Angew. Chem
, vol.118
, pp. 8064
-
-
Hashmi, A.S.K.1
Hutchings, G.J.2
-
37
-
-
33845546747
-
-
Angew. Chem. Int. Ed. 2006, 45, 7896;
-
(2006)
Chem. Int. Ed
, vol.45
, pp. 7896
-
-
Angew1
-
38
-
-
33750061955
-
-
For gold-catalyzed cyclizations of α- and β-allenols, see: b
-
For gold-catalyzed cyclizations of α- and β-allenols, see: b) B. Gockel, N. Krause, Org. Lett. 2006, 8, 4485;
-
(2006)
Org. Lett
, vol.8
, pp. 4485
-
-
Gockel, B.1
Krause, N.2
-
40
-
-
34547504770
-
-
For enantioselective gold-catalyzed cycloisomerization of γ- and δ-allenols, see: d
-
For enantioselective gold-catalyzed cycloisomerization of γ- and δ-allenols, see: d) Z. Zhang, R. A. Widenhoefer, Angew. Chem. 2007, 119, 287;
-
(2007)
Angew. Chem
, vol.119
, pp. 287
-
-
Zhang, Z.1
Widenhoefer, R.A.2
-
41
-
-
33846047998
-
-
Angew. Chem. Int. Ed. 2007, 46, 283.
-
(2007)
Chem. Int. Ed
, vol.46
, pp. 283
-
-
Angew1
-
42
-
-
34548620718
-
-
The formation of all-carbon quaternary centers in an asymmetric manner is one of the most difficult problems in organic chemistry, not least because the process requires the creation of a new C-C bond at a hindered center. For recent selected reviews, see: a) Quaternary Stereocenters: Challenges and Solutions for Organic Synthesis Eds, J. Christoffers. A. Baro, Wiley-VCH, Weinheim, 2005;
-
The formation of all-carbon quaternary centers in an asymmetric manner is one of the most difficult problems in organic chemistry, not least because the process requires the creation of a new C-C bond at a hindered center. For recent selected reviews, see: a) Quaternary Stereocenters: Challenges and Solutions for Organic Synthesis (Eds.: J. Christoffers. A. Baro), Wiley-VCH, Weinheim, 2005;
-
-
-
-
44
-
-
0037162739
-
-
As far as we know, the Pd-catalyzed cyclizative coupling reaction of γ-allenols with allyl halides has not yet been reported. For its pioneering use in α-allenols, see
-
As far as we know, the Pd-catalyzed cyclizative coupling reaction of γ-allenols with allyl halides has not yet been reported. For its pioneering use in α-allenols, see: S. Ma, W. Gao, J. Org. Chem. 2002, 67, 6104.
-
(2002)
J. Org. Chem
, vol.67
, pp. 6104
-
-
Ma, S.1
Gao, W.2
-
45
-
-
0003463148
-
-
To the best of our knowledge, no truly catalytic deprotection of MOM ethers has previously been reported. For comprehensive reviews, see: a, 4th ed, Wiley, New York
-
To the best of our knowledge, no truly catalytic deprotection of MOM ethers has previously been reported. For comprehensive reviews, see: a) P. G. M. Wutz, T. W. Greene, Protective Groups in Organic Synthesis, 4th ed., Wiley, New York, 2006;
-
(2006)
Protective Groups in Organic Synthesis
-
-
Wutz, P.G.M.1
Greene, T.W.2
-
47
-
-
34548628297
-
-
Bicyclic compounds 4, 5, and 8 also possess a β-lactam moiety, which is the key structural motif in biologically relevant compounds such as antibiotics and enzyme inhibitors. For selected reviews, see: a Chemistry and Biology of β-Lactam Antibiotics, Vols. 1-3 (Eds.: R. B. Morin, M. Gorman), Academic Press, New York, 1982;
-
Bicyclic compounds 4, 5, and 8 also possess a β-lactam moiety, which is the key structural motif in biologically relevant compounds such as antibiotics and enzyme inhibitors. For selected reviews, see: a) Chemistry and Biology of β-Lactam Antibiotics, Vols. 1-3 (Eds.: R. B. Morin, M. Gorman), Academic Press, New York, 1982;
-
-
-
-
48
-
-
0001117281
-
-
Ed, G. Lukacs, Springer, Berlin
-
b) R. Southgate, C. Branch, S. Coulton, E. Hunt in Recent Progress in the Chemical Synthesis of Antibiotics and Related Microbial Products, Vol. 2 (Ed.: G. Lukacs), Springer, Berlin, 1993, p. 621;
-
(1993)
Recent Progress in the Chemical Synthesis of Antibiotics and Related Microbial Products
, vol.2
, pp. 621
-
-
Southgate, R.1
Branch, C.2
Coulton, S.3
Hunt, E.4
-
49
-
-
0042423395
-
-
c) G. Veinberg, M. Vorona, I. Shestakova, I. Kanepe, E. Lukevics, Curr. Med. Chem. 2003, 10, 1741.
-
(2003)
Curr. Med. Chem
, vol.10
, pp. 1741
-
-
Veinberg, G.1
Vorona, M.2
Shestakova, I.3
Kanepe, I.4
Lukevics, E.5
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