-
1
-
-
77955716708
-
-
For selected reviews and references
-
For selected reviews and references;
-
-
-
-
4
-
-
63449090271
-
-
I. Kock, S. Draeger, B. Schulz, B. Elsässer, T. Kurtán, A. Kenéz, S. Antus, G. Pescitelli, P. Salvadori, J.-B. Speakman, J. Rheinheimer, and K. Krohn Eur. J. Org. Chem. 2009 1427
-
(2009)
Eur. J. Org. Chem.
, pp. 1427
-
-
Kock, I.1
Draeger, S.2
Schulz, B.3
Elsässer, B.4
Kurtán, T.5
Kenéz, A.6
Antus, S.7
Pescitelli, G.8
Salvadori, P.9
Speakman, J.-B.10
Rheinheimer, J.11
Krohn, K.12
-
8
-
-
77955716509
-
-
For selected reviews
-
For selected reviews;
-
-
-
-
12
-
-
77955714193
-
-
Some selected references
-
Some selected references;
-
-
-
-
15
-
-
33744459738
-
-
For alkyne: D. Hildebrandt, W. Hüggenberg, M. Kanthak, T. Plöger, I.M. Müller, and G. Dyker Chem. Commun. 2006 2260
-
(2006)
Chem. Commun.
, pp. 2260
-
-
Hildebrandt, D.1
Hüggenberg, W.2
Kanthak, M.3
Plöger, T.4
Müller, I.M.5
Dyker, G.6
-
18
-
-
33746299738
-
-
For alkene: N. Asao Synlett 2006 1645
-
(2006)
Synlett
, pp. 1645
-
-
Asao, N.1
-
23
-
-
77955709775
-
-
Some selected reviews
-
Some selected reviews;
-
-
-
-
29
-
-
77955714135
-
-
Dual activation of In(III) catalyst
-
Dual activation of In(III) catalyst:
-
-
-
-
30
-
-
17444379383
-
-
R. Takita, F. Fukuta, R. Tsuji, T. Ohshima, and M. Shibasaki Org. Lett. 7 2005 1363
-
(2005)
Org. Lett.
, vol.7
, pp. 1363
-
-
Takita, R.1
Fukuta, F.2
Tsuji, R.3
Ohshima, T.4
Shibasaki, M.5
-
33
-
-
34250169005
-
-
S. Obika, H. Kono, Y. Yasui, R. Yanada, and Y. Takemoto J. Org. Chem. 72 2007 4462
-
(2007)
J. Org. Chem.
, vol.72
, pp. 4462
-
-
Obika, S.1
Kono, H.2
Yasui, Y.3
Yanada, R.4
Takemoto, Y.5
-
37
-
-
77955716276
-
-
CCDC number for compound 5aa; 765568. Compound 9a; 765569. Compound 21; 765571. Compound 25a; 765566. Compound 25b; 765567. Compound 32b; 765570
-
CCDC number for compound 5aa; 765568. Compound 9a; 765569. Compound 21; 765571. Compound 25a; 765566. Compound 25b; 765567. Compound 32b; 765570.
-
-
-
-
40
-
-
77955718083
-
-
3-catalyzed nucleophilic addition/hydroalkylation of aldehydes with unactivated olefins giving tetrahydrofurans
-
3-catalyzed nucleophilic addition/hydroalkylation of aldehydes with unactivated olefins giving tetrahydrofurans:
-
-
-
-
42
-
-
77955711988
-
-
Cyclization mode (5-exo-dig vs 6-endo-dig) of the metal-catalyzed intramolecular hydroxy alkyne cyclization was largely dependent on the substrates, employing metal and conditions
-
Cyclization mode (5-exo-dig vs 6-endo-dig) of the metal-catalyzed intramolecular hydroxy alkyne cyclization was largely dependent on the substrates, employing metal and conditions.
-
-
-
-
44
-
-
34548096663
-
-
A.S.K. Hashmi, S. Schäfer, M. Wölfle, C.D. Gil, P. Fischer, A. Laguna, M.C. Blanco, and M.C. Gimeno Angew. Chem. Int. Ed. 46 2007 6184
-
(2007)
Angew. Chem. Int. Ed.
, vol.46
, pp. 6184
-
-
Hashmi, A.S.K.1
Schäfer, S.2
Wölfle, M.3
Gil, C.D.4
Fischer, P.5
Laguna, A.6
Blanco, M.C.7
Gimeno, M.C.8
-
46
-
-
42049119847
-
-
Y. Zhang, J. Xue, Z. Xin, Z. Xie, and Y. Li Synlett 2008 940
-
(2008)
Synlett
, pp. 940
-
-
Zhang, Y.1
Xue, J.2
Xin, Z.3
Xie, Z.4
Li, Y.5
-
47
-
-
77955708978
-
-
Some reviews
-
Some reviews:
-
-
-
-
49
-
-
34247624723
-
-
Wiley New Jersey
-
M. Uemura Organic Reactions vol. 67 2006 Wiley New Jersey 217
-
(2006)
Organic Reactions
, vol.67
, pp. 217
-
-
Uemura, M.1
-
53
-
-
77955716397
-
-
An effect of the substituent on the regioselectivity of the cyclization
-
An effect of the substituent on the regioselectivity of the cyclization.
-
-
-
-
55
-
-
33847031343
-
-
H.-P. Bi, L.-N. Guo, X.-H. Duan, F.-R. Gou, S.-H. Huang, X.-Y. Liu, and Y.-M. Liang Org. Lett. 9 2007 397
-
(2007)
Org. Lett.
, vol.9
, pp. 397
-
-
Bi, H.-P.1
Guo, L.-N.2
Duan, X.-H.3
Gou, F.-R.4
Huang, S.-H.5
Liu, X.-Y.6
Liang, Y.-M.7
-
58
-
-
48249154636
-
-
I. Cikotiene, M. Morkunas, D. Motiejaitis, S. Rudys, and A. Brukstus Synlett 2008 1693
-
(2008)
Synlett
, pp. 1693
-
-
Cikotiene, I.1
Morkunas, M.2
Motiejaitis, D.3
Rudys, S.4
Brukstus, A.5
-
61
-
-
85086813702
-
-
Sarker et al reported that similar p-methoxyphenyl substituted benzaldimine chromium complexes gave addition products by scandium trifrate-catalyzed reaction with enol silyl ethers. However, the compound 29a gave no addition products under the reported conditions B.C. Maity, V.G. Puranic, and A. Sarkar Synlett 2002 504
-
(2002)
Synlett
, pp. 504
-
-
Maity, B.C.1
Puranic, V.G.2
Sarkar, A.3
|