-
1
-
-
0003979828
-
-
Academic Press: San Diego
-
Sundberg, R. J. Indoles; Academic Press: San Diego, 1996.
-
(1996)
Indoles
-
-
Sundberg, R.J.1
-
2
-
-
33646557360
-
Palladium-catalyzed enantioselective C-3 allylation of 3-substituted-1H-indoles using trialkylboranes
-
Trost, B. M.; Quancard, J. Palladium-catalyzed enantioselective C-3 allylation of 3-substituted-1H-indoles using trialkylboranes. J. Am. Chem. Soc. 2006, 128, 6314.
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 6314
-
-
Trost, B.M.1
Quancard, J.2
-
3
-
-
32244447519
-
Highly enantioselective synthesis of tetrahydro-ß-carbolines and tetrahydro-γ-carbolines via Pd-catalyzed intramolecular allylic alkylation
-
Bandini, M.; Melloni, A.; Piccinelli, F.; Sinisi, R.; Tommasi, S.; Umani-Ronchi, A. Highly enantioselective synthesis of tetrahydro-ß- carbolines and tetrahydro-γ-carbolines via Pd-catalyzed intramolecular allylic alkylation. J. Am. Chem. Soc. 2006, 128, 1424.
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 1424
-
-
Bandini, M.1
Melloni, A.2
Piccinelli, F.3
Sinisi, R.4
Tommasi, S.5
Umani-Ronchi, A.6
-
4
-
-
11144283570
-
First example of the C-alkylation of indoles with Baylis-Hillman acetates
-
Yadav, J. S.; Reddy, B. V. S.; Basak, A. K.; Narsaiah, A. V.; Prabhakar, A.; Jagadeesh, B. First example of the C-alkylation of indoles with Baylis-Hillman acetates. Tetrahedron Lett. 2005, 46, 639.
-
(2005)
Tetrahedron Lett.
, vol.46
, pp. 639
-
-
Yadav, J.S.1
Reddy, B.V.S.2
Basak, A.K.3
Narsaiah, A.V.4
Prabhakar, A.5
Jagadeesh, B.6
-
5
-
-
33750308939
-
Electrophilic allylations and benzylations of indoles in neutral aqueous or alcoholic solutions
-
Westermaier, M.; Mayr, H. Electrophilic allylations and benzylations of indoles in neutral aqueous or alcoholic solutions. Org. Lett. 2006, 8, 4791.
-
(2006)
Org. Lett.
, vol.8
, pp. 4791
-
-
Westermaier, M.1
Mayr, H.2
-
6
-
-
33646073412
-
Novel gallium-mediated C3-allylation of indoles and pyrroles in aqueous media promoted by Bu4NBr
-
Prajapati, D.; Gohain, M.; Gogoi, B. J. Novel gallium-mediated C3-allylation of indoles and pyrroles in aqueous media promoted by Bu4NBr. Tetrahedron Lett. 2006, 47, 3535.
-
(2006)
Tetrahedron Lett.
, vol.47
, pp. 3535
-
-
Prajapati, D.1
Gohain, M.2
Gogoi, B.J.3
-
7
-
-
0037100115
-
Zinc-mediated Barbier reactions of pyrroles and indoles: A new method for the alkylation of pyrroles and indoles
-
Yadav, J. S.; Reddy, B. V. S.; Muralikrishna, P.; Srinivas, C. Zinc-mediated Barbier reactions of pyrroles and indoles: A new method for the alkylation of pyrroles and indoles. Tetrahedron Lett. 2002, 43, 5185.
-
(2002)
Tetrahedron Lett.
, vol.43
, pp. 5185
-
-
Yadav, J.S.1
Reddy, B.V.S.2
Muralikrishna, P.3
Srinivas, C.4
-
8
-
-
5144230655
-
Palladium-catalyzed functionalization of indoles with 2-acetoxymethyl substituted electron-deficient alkenes
-
Ma, S.-M.; Yu, S.-C. Palladium-catalyzed functionalization of indoles with 2-acetoxymethyl substituted electron-deficient alkenes. Tetrahedron Lett. 2004, 45, 8419.
-
(2004)
Tetrahedron Lett.
, vol.45
, pp. 8419
-
-
Ma, S.-M.1
Yu, S.-C.2
-
9
-
-
16844383145
-
Pd-catalyzed C3-selective allylation of indoles with allyl alcohols promoted by triethylborane
-
Kimura, M.; Futamata, M.; Mukai, R.; Tamaru, Y. Pd-catalyzed C3-selective allylation of indoles with allyl alcohols promoted by triethylborane. J. Am. Chem. Soc. 2005, 127, 4592.
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 4592
-
-
Kimura, M.1
Futamata, M.2
Mukai, R.3
Tamaru, Y.4
-
10
-
-
4544324311
-
New versatile Pd-catalyzed alkylation of indoles via nucleophilic alyllic substitution: Controlling the regioselectivity
-
Bandini, M.; Melloni, A.; Umani-Ronchi, A. New versatile Pd-catalyzed alkylation of indoles via nucleophilic alyllic substitution: Controlling the regioselectivity. Org. Lett. 2004, 6, 3199.
-
(2004)
Org. Lett.
, vol.6
, pp. 3199
-
-
Bandini, M.1
Melloni, A.2
Umani-Ronchi, A.3
-
11
-
-
0037071923
-
Regio-, and enantioselective Pd-catalyzed allylic alkylation of indolocarbazole pro-aglycons
-
Trost, B. M.; Krische, M. J.; Berl, V.; Grenzer, E. M. Chemo-, regio-, and enantioselective Pd-catalyzed allylic alkylation of indolocarbazole pro-aglycons. Org. Lett. 2002, 4, 2005.
-
(2002)
Org. Lett.
, vol.4
, pp. 2005
-
-
Trost, B.M.1
Krische, M.J.2
Berl, V.3
Chemo, G.M.E.4
-
12
-
-
0000478083
-
Synthesis of prenylated indoles
-
Wenkert, E.; Angell, E. C.; Ferreira, V. F.; Michelotti, E. L.; Piettre, S. R.; Sheu, J.-H.; Swindell, C. S. Synthesis of prenylated indoles. J. Org. Chem. 1986, 51, 2343.
-
(1986)
J. Org. Chem.
, vol.51
, pp. 2343
-
-
Wenkert, E.1
Angell, E.C.2
Ferreira, V.F.3
Michelotti, E.L.4
Piettre, S.R.5
Sheu, J.-H.6
Swindell, C.S.7
-
13
-
-
0010518961
-
Palladium-catalyzed allylation of indoles
-
Billups, W. E.; Erkes, R. S.; Reed, L. E. Palladium-catalyzed allylation of indoles. Synth. Commun. 1980, 10, 147.
-
(1980)
Synth. Commun.
, vol.10
, pp. 147
-
-
Billups, W.E.1
Erkes, R.S.2
Reed, L.E.3
-
14
-
-
0033574653
-
Molybdenum(II)-catalyzed allylation of electron-rich aromatics and heteroaromatics
-
Malkov, A. V.; Davis, S. L.; Baxendale, I. R.; Mitchell, W. L.; Kocovsky, P. Molybdenum(II)-catalyzed allylation of electron-rich aromatics and heteroaromatics. J. Org. Chem. 1999, 64, 2751.
-
(1999)
J. Org. Chem.
, vol.64
, pp. 2751
-
-
Malkov, A.V.1
Davis, S.L.2
Baxendale, I.R.3
Mitchell, W.L.4
Kocovsky, P.5
-
15
-
-
0001398838
-
Co(III) DMG-catalyzed synthesis of allylamides from allyl alcohols and acetonitrile
-
Mukhopadhyay, M.; Iqbal, J. Co(III)DMG-catalyzed synthesis of allylamides from allyl alcohols and acetonitrile. J. Org. Chem. 1997, 62, 1843.
-
(1997)
J. Org. Chem.
, vol.62
, pp. 1843
-
-
Mukhopadhyay, M.1
Iqbal, J.2
-
16
-
-
31444456960
-
Direct carbon-carbon bond formation from alcohols and active methylenes, alkoxyketones, or indoles catalyzed by indium trichloride
-
Yasuda, M.; Somyo, T.; Baba, A. Direct carbon-carbon bond formation from alcohols and active methylenes, alkoxyketones, or indoles catalyzed by indium trichloride. Angew. Chem. Int. Ed. 2006, 45, 793.
-
(2006)
Angew. Chem. Int. Ed.
, vol.45
, pp. 793
-
-
Yasuda, M.1
Somyo, T.2
Baba, A.3
-
17
-
-
0000284687
-
Scandium(III) triflate-catalyzed Friedel-Crafts alkylation reactions
-
Tsuchimoto, T.; Tobita, K.; Hiyama, T.; Fukuzawa, S.-I. Scandium(III) triflate-catalyzed Friedel-Crafts alkylation reactions. J. Org. Chem. 1997, 62, 6997.
-
(1997)
J. Org. Chem.
, vol.62
, pp. 6997
-
-
Tsuchimoto, T.1
Tobita, K.2
Hiyama, T.3
Fukuzawa, S.-I.4
-
18
-
-
0040753494
-
Scandium (III) triflate-catalyzed Friedel-Crafts alkylations with benzyl and allyl alcohols
-
Tsuchimoto, T.; Tobita, K.; Hiyama, T.; Fukuzawa, S.-I. Scandium(III) triflate-catalyzed Friedel-Crafts alkylations with benzyl and allyl alcohols. Synlett. 1996, 557.
-
(1996)
Synlett.
, vol.557
-
-
Tsuchimoto, T.1
Tobita, K.2
Hiyama, T.3
Fukuzawa, S.-I.4
-
20
-
-
5344246652
-
An efficient and inexpensive catalyst system for Friedel-Crafts alkylation of aromatic compounds with benzyl and allyl alcohols
-
Li, J.-H.; Liu, W.-J.; Yin, D.-L. An efficient and inexpensive catalyst system for Friedel-Crafts alkylation of aromatic compounds with benzyl and allyl alcohols. Synth. Commun. 2004, 34, 3161.
-
(2004)
Synth. Commun.
, vol.34
, pp. 3161
-
-
Li, J.-H.1
Liu, W.-J.2
Yin, D.-L.3
-
21
-
-
0037134217
-
Regioselective synthesis of 3-alkylindoles mediated by zinc triflate
-
Zhu, X.; Ganesan, A. Regioselective synthesis of 3-alkylindoles mediated by zinc triflate. J. Org. Chem. 2002, 67, 2705.
-
(2002)
J. Org. Chem.
, vol.67
, pp. 2705
-
-
Zhu, X.1
Ganesan, A.2
-
22
-
-
33846451020
-
Bismuth-catalyzed direct substitution of the hydroxy group in alcohols with sulfonamides, carbamates, and carboxamides
-
Qin, H.; Yamagiwa, N.; Matsunaga, S.; Shibasaki, M. Bismuth-catalyzed direct substitution of the hydroxy group in alcohols with sulfonamides, carbamates, and carboxamides. Angew. Chem. Int. Ed. 2007, 46, 409.
-
(2007)
Angew. Chem. Int. Ed.
, vol.46
, pp. 409
-
-
Qin, H.1
Yamagiwa, N.2
Matsunaga, S.3
Shibasaki, M.4
-
24
-
-
0036736778
-
Solid acids for green chemistry
-
Clark, J.-H. Solid acids for green chemistry. Acc. Chem. Res. 2002, 35, 791.
-
(2002)
Acc. Chem. Res.
, vol.35
, pp. 791
-
-
Clark, J.-H.1
-
25
-
-
14544287742
-
Regio- and stereoselective ring opening of 2,3-diaryl oxiranes by LiBr/Amberlyst-15: A new stereocontrolled access to 1,2-diaryl-2-bromo alcohols
-
Arlette, S.-C.; Paolo, L.; Carlo, B. Regio- and stereoselective ring opening of 2,3-diaryl oxiranes by LiBr/Amberlyst-15: A new stereocontrolled access to 1,2-diaryl-2-bromo alcohols. J. Org. Chem. 2005, 70, 1605.
-
(2005)
J. Org. Chem.
, vol.70
, pp. 1605
-
-
Arlette, S.-C.1
Paolo, L.2
Carlo, B.3
-
26
-
-
33644599352
-
Amberlyst-15: An efficient reusable heterogeneous catalyst for the synthesis of 1,8-dioxo-octahydroxanthenes and 1,8-dioxo-decahydroacridines
-
Das, B.; Thirupathi, P.; Mahender, I.; Reddy, V. S.; Rao, Y. K. Amberlyst-15: An efficient reusable heterogeneous catalyst for the synthesis of 1,8-dioxo-octahydroxanthenes and 1,8-dioxo-decahydroacridines. J. Mol. Catal. A 2006, 247, 233.
-
(2006)
J. Mol. Catal. A
, vol.247
, pp. 233
-
-
Das, B.1
Thirupathi, P.2
Mahender, I.3
Reddy, V.S.4
Rao, Y.K.5
-
27
-
-
33750494718
-
A convenient highly stereoselective synthesis of allyl amides from Baylis-Hillman adducts using Amberlyst-15 as a heterogeneous reusable catalyst
-
Das, B.; Majhi, A.; Banerjee, J.; Chowdhury, N. A convenient highly stereoselective synthesis of allyl amides from Baylis-Hillman adducts using Amberlyst-15 as a heterogeneous reusable catalyst. J. Mol. Catal. A 2006, 260, 32.
-
(2006)
J. Mol. Catal. A
, vol.260
, pp. 32
-
-
Das, B.1
Majhi, A.2
Banerjee, J.3
Chowdhury, N.4
-
28
-
-
13244256989
-
Amberlyst-15 as a novel and recyclable solid acid for the coupling of aromatic aldehydes with homopropargyl alcohol
-
Yadav, J. S.; Reddy, B. V. S.; Vishnumurthy, P. Amberlyst-15 as a novel and recyclable solid acid for the coupling of aromatic aldehydes with homopropargyl alcohol. Tetrahedron Lett. 2005, 46, 1311.
-
(2005)
Tetrahedron Lett.
, vol.46
, pp. 1311
-
-
Yadav, J.S.1
Reddy, B.V.S.2
Vishnumurthy, P.3
-
29
-
-
11144267793
-
Amberlyst-15-promoted efficient 2-halogenation of 1,3-keto-esters and cyclic ketones using N-halosuccinimides
-
Meshram, H. M.; Reddy, P. N.; Sadashiv, K.; Yadav, J. S. Amberlyst-15-promoted efficient 2-halogenation of 1,3-keto-esters and cyclic ketones using N-halosuccinimides. Tetrahedron Lett. 2005, 46, 623.
-
(2005)
Tetrahedron Lett.
, vol.46
, pp. 623
-
-
Meshram, H.M.1
Reddy, P.N.2
Sadashiv, K.3
Yadav, J.S.4
-
30
-
-
0037525480
-
Selective deprotection of aromatic acetates catalyzed by Amberlyst-15 or iodine
-
Das, B.; Banerjee, J.; Ramu, R.; Pal, R.; Ravindranath, N.; Ramesh, C. Efficient, selective deprotection of aromatic acetates catalyzed by Amberlyst-15 or iodine. Tetrahedron Lett. 2003, 44, 5465.
-
(2003)
Tetrahedron Lett.
, vol.44
, pp. 5465
-
-
Das, B.1
Banerjee, J.2
Ramu, R.3
Pal, R.4
Ravindranath, N.5
Efficient, R.C.6
|