-
2
-
-
77349099243
-
C-H bond activations by metal oxo compounds
-
10.1021/cr900269x 20143877 10.1021/cr900269x 1:CAS:528: DC%2BC3cXhsF2rurw%3D
-
Gunay A, Theopold KH (2010) C-H bond activations by metal oxo compounds. Chem Rev 110:1060-1081. doi: 10.1021/cr900269x
-
(2010)
Chem Rev
, vol.110
, pp. 1060-1081
-
-
Gunay, A.1
Theopold, K.H.2
-
3
-
-
79952634665
-
Carboxylate-assisted transition-metal-catalyzed C-H bond functionalizations: Mechanism and scope
-
10.1021/cr100412j 21391562 10.1021/cr100412j 1:CAS:528: DC%2BC3MXivVSgt7k%3D
-
Ackermann L (2011) Carboxylate-assisted transition-metal-catalyzed C-H bond functionalizations: mechanism and scope. Chem Rev 111:1315-1345. doi: 10.1021/cr100412j
-
(2011)
Chem Rev
, vol.111
, pp. 1315-1345
-
-
Ackermann, L.1
-
4
-
-
33846918696
-
Aryl-aryl bond formation by transition-metal-catalyzed direct arylation
-
10.1021/cr0509760 17212475 10.1021/cr0509760 1:CAS:528: DC%2BD2sXis12hsg%3D%3D
-
Alberico D, Scott ME, Lautens M (2007) Aryl-aryl bond formation by transition-metal-catalyzed direct arylation. Chem Rev 107: 174-238. doi: 10.1021/cr0509760
-
(2007)
Chem Rev
, vol.107
, pp. 174-238
-
-
Alberico, D.1
Scott, M.E.2
Lautens, M.3
-
5
-
-
67649488045
-
Palladium(II)-catalyzed C-H activation/C-C cross-coupling reactions: Versatility and practicality
-
10.1002/anie.200806273 10.1002/anie.200806273 1:CAS:528: DC%2BD1MXotVegu7k%3D
-
Chen X, Engle KM, Wang DH, Yu JQ (2009) Palladium(II)-catalyzed C-H activation/C-C cross-coupling reactions: versatility and practicality. Angew Chem Int Ed 48:5094-5115. doi: 10.1002/anie.200806273
-
(2009)
Angew Chem Int Ed
, vol.48
, pp. 5094-5115
-
-
Chen, X.1
Engle, K.M.2
Wang, D.H.3
Yu, J.Q.4
-
6
-
-
33646152128
-
Aryl transfer between Pd(II) centers or Pd(IV) intermediates in Pd-catalyzed domino reactions
-
10.1021/ja056661j 16608337 10.1021/ja056661j 1:CAS:528: DC%2BD28XislCjsb8%3D
-
Cardenas DJ, Martin-Matute B, Echavarren AM (2006) Aryl transfer between Pd(II) centers or Pd(IV) intermediates in Pd-catalyzed domino reactions. J Am Chem Soc 128:5033-5040. doi: 10.1021/ja056661j
-
(2006)
J Am Chem Soc
, vol.128
, pp. 5033-5040
-
-
Cardenas, D.J.1
Martin-Matute, B.2
Echavarren, A.M.3
-
7
-
-
33747071481
-
Selected patented cross-coupling reaction technologies
-
10.1021/cr0505268 16836296 10.1021/cr0505268 1:CAS:528: DC%2BD28XmsVeltLk%3D
-
Corbet JP, Mignani G (2006) Selected patented cross-coupling reaction technologies. Chem Rev 106:2651-2710. doi: 10.1021/cr0505268
-
(2006)
Chem Rev
, vol.106
, pp. 2651-2710
-
-
Corbet, J.P.1
Mignani, G.2
-
8
-
-
79952656192
-
Advances in transition metal (Pd, Ni, Fe)-catalyzed cross-coupling reactions using alkyl-organometallics as reaction partners
-
10.1021/cr100327p 21319862 10.1021/cr100327p 1:CAS:528: DC%2BC3MXhvFeisbk%3D
-
Jana R, Pathak TP, Sigman MS (2011) Advances in transition metal (Pd, Ni, Fe)-catalyzed cross-coupling reactions using alkyl-organometallics as reaction partners. Chem Rev 111:1417-1492. doi: 10.1021/cr100327p
-
(2011)
Chem Rev
, vol.111
, pp. 1417-1492
-
-
Jana, R.1
Pathak, T.P.2
Sigman, M.S.3
-
9
-
-
0036589261
-
Ru-, Rh-, and Pd-catalyzed C-C bond formation involving C-H activation and addition on unsaturated substrates?: Reactions and mechanistic aspects
-
10.1021/cr0104330 11996548 10.1021/cr0104330 1:CAS:528: DC%2BD38XisFSgtr8%3D
-
Ritleng V, Sirlin C, Pfeffer M (2002) Ru-, Rh-, and Pd-catalyzed C-C bond formation involving C-H activation and addition on unsaturated substrates?: reactions and mechanistic aspects. Chem Rev 102:1731-1770. doi: 10.1021/cr0104330
-
(2002)
Chem Rev
, vol.102
, pp. 1731-1770
-
-
Ritleng, V.1
Sirlin, C.2
Pfeffer, M.3
-
10
-
-
79952675758
-
Direct C-H transformation via iron catalysis
-
10.1021/cr100198w 21049955 10.1021/cr100198w 1:CAS:528:DC%2BC3cXhtlyhtLbN
-
Sun CL, Li BJ, Shi ZJ (2011) Direct C-H transformation via iron catalysis. Chem Rev 111:1293-1314. doi: 10.1021/cr100198w
-
(2011)
Chem Rev
, vol.111
, pp. 1293-1314
-
-
Sun, C.L.1
Li, B.J.2
Shi, Z.J.3
-
11
-
-
84869476909
-
Acetamide as cocatalyst for the nitrogen-directed coupling of arenes with aryl chlorides through ruthenium-catalyzed C-H activation
-
doi: 10.1002/ejoc.201201127
-
Zhang J, Yang Q, Zhu Z, Yuan ML, Fu HY, Zheng XL, Chen H, Li RX (2012) Acetamide as cocatalyst for the nitrogen-directed coupling of arenes with aryl chlorides through ruthenium-catalyzed C-H activation. Eur J Org Chem 6702-6706. doi: 10.1002/ejoc.201201127
-
(2012)
Eur J Org Chem
, pp. 6702-6706
-
-
Zhang, J.1
Yang, Q.2
Zhu, Z.3
Yuan, M.L.4
Fu, H.Y.5
Zheng, X.L.6
Chen, H.7
Li, R.X.8
-
12
-
-
21244438753
-
Anilide ortho-arylation by using C-H activation methodology
-
10.1002/anie.200500589 10.1002/anie.200500589 1:CAS:528: DC%2BD2MXmtF2gsr0%3D
-
Daugulis O, Zaitsev VG (2005) Anilide ortho-arylation by using C-H activation methodology. Angew Chem Int Ed 44:4046-4048. doi: 10.1002/anie.200500589
-
(2005)
Angew Chem Int Ed
, vol.44
, pp. 4046-4048
-
-
Daugulis, O.1
Zaitsev, V.G.2
-
13
-
-
77955405522
-
Investigation of the mechanism of C(sp 3) -H bond cleavage in Pd(0)-catalyzed intramolecular alkane arylation adjacent to amides and sulfonamides
-
10.1021/ja103081n 20681702 10.1021/ja103081n 1:CAS:528: DC%2BC3cXptFOrurs%3D
-
Rousseaux S, Gorelsky S, Chung BKW, Fagnou K (2010) Investigation of the mechanism of C(sp 3) -H bond cleavage in Pd(0)-catalyzed intramolecular alkane arylation adjacent to amides and sulfonamides. J Am Chem Soc 132:10692-10705. doi: 10.1021/ja103081n
-
(2010)
J Am Chem Soc
, vol.132
, pp. 10692-10705
-
-
Rousseaux, S.1
Gorelsky, S.2
Chung, B.K.W.3
Fagnou, K.4
-
14
-
-
45249095830
-
Direct ortho-acetoxylation of anilides via palladium-catalyzed sp 2 C-H bond oxidative activation
-
10.1021/jo8003088 10.1021/jo8003088
-
Wang GW, Yuan TT, Wu XL (2008) Direct ortho-acetoxylation of anilides via palladium-catalyzed sp 2 C-H bond oxidative activation. J Org Chem 71:4717-4720. doi: 10.1021/jo8003088
-
(2008)
J Org Chem
, vol.71
, pp. 4717-4720
-
-
Wang, G.W.1
Yuan, T.T.2
Wu, X.L.3
-
15
-
-
21944441002
-
The potential of palladacycles?: More than just precatalysts
-
10.1021/cr030681r 15941221 10.1021/cr030681r 1:CAS:528: DC%2BD2MXksVWjsbY%3D
-
Dupont J, Consorti CS, Spencer J (2005) The potential of palladacycles?: more than just precatalysts. Chem Rev 105:2527-2572. doi: 10.1021/cr030681r
-
(2005)
Chem Rev
, vol.105
, pp. 2527-2572
-
-
Dupont, J.1
Consorti, C.S.2
Spencer, J.3
-
16
-
-
34249056813
-
Ortho arylation of acetanilides via Pd(II)-catalyzed C-H functionalization
-
10.1021/ja070767s 17455938 10.1021/ja070767s 1:CAS:528: DC%2BD2sXksFSns7w%3D
-
Yang S, Li B, Wan X, Shi Z (2007) Ortho arylation of acetanilides via Pd(II)-catalyzed C-H functionalization. J Am Chem Soc 129:6066-6067. doi: 10.1021/ja070767s
-
(2007)
J Am Chem Soc
, vol.129
, pp. 6066-6067
-
-
Yang, S.1
Li, B.2
Wan, X.3
Shi, Z.4
-
17
-
-
33749509027
-
Palladium-catalyzed alkylation of sp 2 and sp 3 C-H bonds with methylboroxine and alkylboronic acids?: Two distinct C-H activation pathways
-
10.1021/ja0646747 10.1021/ja0646747
-
Chen X, Goodhue CE, Yu JQ (2008) Palladium-catalyzed alkylation of sp 2 and sp 3 C-H bonds with methylboroxine and alkylboronic acids?: two distinct C-H activation pathways. J Am Chem Soc 128:12634-12635. doi: 10.1021/ja0646747
-
(2008)
J Am Chem Soc
, vol.128
, pp. 12634-12635
-
-
Chen, X.1
Goodhue, C.E.2
Yu, J.Q.3
-
18
-
-
77949381429
-
Palladium-catalyzed ligand-directed C-H functionalization reactions
-
10.1021/cr900184e 20078038 10.1021/cr900184e 1:CAS:528: DC%2BC3cXmslWksQ%3D%3D
-
Lyons TW, Sanford MS (2010) Palladium-catalyzed ligand-directed C-H functionalization reactions. Chem Rev 110: 1147-1169. doi: 10.1021/cr900184e
-
(2010)
Chem Rev
, vol.110
, pp. 1147-1169
-
-
Lyons, T.W.1
Sanford, M.S.2
-
19
-
-
77954310776
-
Antimicrobial activity and a SAR study of some novel benzimidazole derivatives bearing hydrazones moiety
-
10.1016/j.ejmech.2010.04.012 20451306 10.1016/j.ejmech.2010.04.012
-
Ozkay Y, Tunali Y, Karaca H, Isikdag I (2010) Antimicrobial activity and a SAR study of some novel benzimidazole derivatives bearing hydrazones moiety. Eur J Med Chem 45:3293-3298. doi: 10.1016/j.ejmech.2010.04.012
-
(2010)
Eur J Med Chem
, vol.45
, pp. 3293-3298
-
-
Ozkay, Y.1
Tunali, Y.2
Karaca, H.3
Isikdag, I.4
-
20
-
-
80054952210
-
Synthesis and biological evaluation of novel analogues of the pan class i phosphatidylinositol 3-kinase (PI3K) inhibitor 2-(difluoromethyl)-1-[4,6-di (4-morpholinyl)-1,3,5-triazin-2-yl]-1 H -benzimidazole (ZSTK474)
-
doi: 10.1021/jm200688y
-
Rewcastle GW, Gamage SA, Flanagan JU, Frederick R, Denny WA, Baguley BC, Kestell P, Singh R, Kendall JD, Marshall ES, Lill CL, Lee WJ, Kolekar S, Buchanan CM, Jamieson SMF, Shepherd PR (2011) Synthesis and biological evaluation of novel analogues of the pan class I phosphatidylinositol 3-kinase (PI3K) inhibitor 2-(difluoromethyl)-1-[4,6-di (4-morpholinyl)-1,3,5-triazin-2- yl]-1 H -benzimidazole (ZSTK474). J Med Chem 54:7105-7126. doi: 10.1021/jm200688y
-
(2011)
J Med Chem
, vol.54
, pp. 7105-7126
-
-
Rewcastle, G.W.1
Gamage, S.A.2
Flanagan, J.U.3
Frederick, R.4
Denny, W.A.5
Baguley, B.C.6
Kestell, P.7
Singh, R.8
Kendall, J.D.9
Marshall, E.S.10
Lill, C.L.11
Lee, W.J.12
Kolekar, S.13
Buchanan, C.M.14
Smf, J.15
Shepherd, P.R.16
-
21
-
-
84886089913
-
-
US Patent 00608070A
-
Anthony NJ, Gomez RP, Stokker GE, Wai JS, Williams TM, Halczenko W, Hutchinson JH, Young SD, Solinsky KM (2000) US Patent 00608070A
-
(2000)
-
-
Anthony, N.J.1
Gomez, R.P.2
Stokker, G.E.3
Wai, J.S.4
Williams, T.M.5
Halczenko, W.6
Hutchinson, J.H.7
Young, S.D.8
Solinsky, K.M.9
-
22
-
-
33646560007
-
Synthesis and biological evaluation of benzimidazole derivatives as potent AMP-activated protein kinase activators
-
10.1016/j.bmc.2006.02.028 16513356 10.1016/j.bmc.2006.02.028 1:CAS:528:DC%2BD28XltVGqtr8%3D
-
Charton J, Girault-Mizzi S, Debreu-Fontaine MA, Foufelle F, Hainault I, Bizot-Espiard JG, Caignard DH, Sergheraert C (2006) Synthesis and biological evaluation of benzimidazole derivatives as potent AMP-activated protein kinase activators. Bioorg Med Chem 14:4490-4518. doi: 10.1016/j.bmc.2006.02.028
-
(2006)
Bioorg Med Chem
, vol.14
, pp. 4490-4518
-
-
Charton, J.1
Girault-Mizzi, S.2
Debreu-Fontaine, M.A.3
Foufelle, F.4
Hainault, I.5
Bizot-Espiard, J.G.6
Caignard, D.H.7
Sergheraert, C.8
-
23
-
-
77956176991
-
Substituted biaryl oxazoles, imidazoles, and thiazoles as sodium channel blockers
-
10.1016/j.bmcl.2010.07.064 20709552 10.1016/j.bmcl.2010.07.064 1:CAS:528:DC%2BC3cXhtV2jt7vP
-
Tyagarajan S, Chakravarty PK, Zhou B, Fisher MH, Wyvratt MJ, Lyons K, Klatt T, Li X, Kumar S, Williams B, Felix J, Priest BT, Brochu RM, Warren V, Smith M, Garcia M, Kaczorowski GJ, Martin WJ, Abbadie C, McGowan E, Jochnowitz N, Parsons WH (2010) Substituted biaryl oxazoles, imidazoles, and thiazoles as sodium channel blockers. Bioorg Med Chem Lett 20:5536-5540. doi: 10.1016/j.bmcl.2010.07.064
-
(2010)
Bioorg Med Chem Lett
, vol.20
, pp. 5536-5540
-
-
Tyagarajan, S.1
Chakravarty, P.K.2
Zhou, B.3
Fisher, M.H.4
Wyvratt, M.J.5
Lyons, K.6
Klatt, T.7
Li, X.8
Kumar, S.9
Williams, B.10
Felix, J.11
Priest, B.T.12
Brochu, R.M.13
Warren, V.14
Smith, M.15
Garcia, M.16
Kaczorowski, G.J.17
Martin, W.J.18
Abbadie, C.19
McGowan, E.20
Jochnowitz, N.21
Parsons, W.H.22
more..
-
24
-
-
1542547460
-
Identification of Telmisartan as a unique angiotensin II receptor antagonist with selective PPAR-modulating activity
-
10.1161/01.HYP.0000123072.34629.57 15007034 10.1161/01.HYP.0000123072. 34629.57 1:CAS:528:DC%2BD2cXjt1GmtrY%3D
-
Benson SC, Pershadsingh H, Ho C, Chittiboyina A, Desai P, Pravenec M, Qi N, Wang J, Avery MA, Kurtz TW (2004) Identification of Telmisartan as a unique angiotensin II receptor antagonist with selective PPAR-modulating activity. Hypertension 43: 993-1002. doi: 10.1161/01.HYP.0000123072.34629.57
-
(2004)
Hypertension
, vol.43
, pp. 993-1002
-
-
Benson, S.C.1
Pershadsingh, H.2
Ho, C.3
Chittiboyina, A.4
Desai, P.5
Pravenec, M.6
Qi, N.7
Wang, J.8
Avery, M.A.9
Kurtz, T.W.10
-
25
-
-
0027240392
-
Nonpeptide angiotensin II receptor antagonists. Synthesis and biological activity of benzimidazolecarboxylic acids
-
doi: 10.1021/jm00067a016
-
Kubo K, Kohara Y, Imamiya E, Sugiura Y, Inada Y, Furukawa Y, Nishikawa K, Naka T (1993) Nonpeptide angiotensin II receptor antagonists. Synthesis and biological activity of benzimidazolecarboxylic acids. J Med Chem 36:2182-2195. doi: 10.1021/jm00067a016
-
(1993)
J Med Chem
, vol.36
, pp. 2182-2195
-
-
Kubo, K.1
Kohara, Y.2
Imamiya, E.3
Sugiura, Y.4
Inada, Y.5
Furukawa, Y.6
Nishikawa, K.7
Naka, T.8
-
26
-
-
23244446601
-
Design, synthesis, and evaluation of novelly substituted benzimidazole compounds as angiotensin II receptor antagonists
-
doi: 10.1016/j.bmcl.2005.05.054
-
Bali A, Bansal Y, Sugumaran M, Saggu JS, Balakumar P, Kaur G, Bansal G, Sharma A, Singh M (2005) Design, synthesis, and evaluation of novelly substituted benzimidazole compounds as angiotensin II receptor antagonists. Bioorg Med Chem Lett 15:3962-3965. doi: 10.1016/j.bmcl.2005.05.054
-
(2005)
Bioorg Med Chem Lett
, vol.15
, pp. 3962-3965
-
-
Bali, A.1
Bansal, Y.2
Sugumaran, M.3
Saggu, J.S.4
Balakumar, P.5
Kaur, G.6
Bansal, G.7
Sharma, A.8
Singh, M.9
-
27
-
-
82255170708
-
Copper-catalyzed, one-pot, three-component synthesis of benzimidazoles by condensation and C-N bond formation
-
10.1021/jo2019416 22034860 10.1021/jo2019416 1:CAS:528:DC%2BC3MXhtlyqsLbI
-
Kim Y, Kumar MR, Park N, Heo Y, Lee S (2011) Copper-catalyzed, one-pot, three-component synthesis of benzimidazoles by condensation and C-N bond formation. J Org Chem 76:9577-9583. doi: 10.1021/jo2019416
-
(2011)
J Org Chem
, vol.76
, pp. 9577-9583
-
-
Kim, Y.1
Kumar, M.R.2
Park, N.3
Heo, Y.4
Lee, S.5
-
28
-
-
84859573433
-
Synthesis of imidazo[4, 5-b]pyridines and imidazo[4,5-b]pyrazines by palladium catalyzed amidation of 2-chloro-3-aminoheterocycles
-
doi: 10.1021/ol300359s
-
Rosenberg AJ, Zhao J, Clark DA (2012) Synthesis of imidazo[4, 5-b]pyridines and imidazo[4,5-b]pyrazines by palladium catalyzed amidation of 2-chloro-3-aminoheterocycles. Org Lett 14: 1764-1767. doi: 10.1021/ol300359s
-
(2012)
Org Lett
, vol.14
, pp. 1764-1767
-
-
Rosenberg, A.J.1
Zhao, J.2
Clark, D.A.3
-
29
-
-
33645087622
-
Palladium- and copper-mediated direct C-2 arylation of azoles-including free (NH)-imidazole, -benzimidazole and -indole - Under base-free and ligandless conditions
-
doi: 10.1002/ejoc.200500957
-
Bellina F, Cauteruccio S, Rossi R (2006) Palladium- and copper-mediated direct C-2 arylation of azoles-including free (NH)-imidazole, -benzimidazole and -indole - under base-free and ligandless conditions. Eur J Org Chem 1379-1382. doi: 10.1002/ejoc.200500957
-
(2006)
Eur J Org Chem
, pp. 1379-1382
-
-
Bellina, F.1
Cauteruccio, S.2
Rossi, R.3
-
30
-
-
19644379034
-
Conversion of sterically hindered diacylated 1,2-phenylenediamines into 2-substituted benzimidazoles
-
Charton J, Girault-Mizzi S, Sergheraert C (2005) Conversion of sterically hindered diacylated 1,2-phenylenediamines into 2-substituted benzimidazoles. Chem Pharm Bull 35: 492-497
-
(2005)
Chem Pharm Bull
, vol.35
, pp. 492-497
-
-
Charton, J.1
Girault-Mizzi, S.2
Sergheraert, C.3
-
31
-
-
1242272139
-
A geometrically constraining bis(benzimidazole) ligand and its nearly tetrahedral complexes with Fe(II) and Mn(II)
-
10.1021/ic030180o 14966985 10.1021/ic030180o 1:CAS:528: DC%2BD2cXktVeltw%3D%3D
-
Stibrany RT, Lobanov MV, Schugar HJ, Potenza JA (2004) A geometrically constraining bis(benzimidazole) ligand and its nearly tetrahedral complexes with Fe(II) and Mn(II). Inorg Chem 43:1472-1480. doi: 10.1021/ic030180o
-
(2004)
Inorg Chem
, vol.43
, pp. 1472-1480
-
-
Stibrany, R.T.1
Lobanov, M.V.2
Schugar, H.J.3
Potenza, J.A.4
-
32
-
-
33947215015
-
Acid-catalyzed solvent-free synthesis of 2-arylbenzimidazoles under microwave irradiation
-
10.1016/j.molcata.2006.04.071 10.1016/j.molcata.2006.04.071 1:CAS:528:DC%2BD2sXjtVegtr8%3D
-
Wang R, Lu XX, Yu XQ, Shi L, Sun Y (2007) Acid-catalyzed solvent-free synthesis of 2-arylbenzimidazoles under microwave irradiation. J Mol Catal A 266:198-201. doi: 10.1016/j.molcata.2006.04.071
-
(2007)
J Mol Catal A
, vol.266
, pp. 198-201
-
-
Wang, R.1
Lu, X.X.2
Yu, X.Q.3
Shi, L.4
Sun, Y.5
-
33
-
-
0033054018
-
Parallel synthesis of polyethylene glycol supported biaryl benzimidazoles and imidazopyridines
-
10.1055/s-1999-2598
-
Blettner CG, Konig WA, Rühter G, Stenzel W, Schotten T (1999) Parallel synthesis of polyethylene glycol supported biaryl benzimidazoles and imidazopyridines. Synlett 3:307-310
-
(1999)
Synlett
, vol.3
, pp. 307-310
-
-
Blettner, C.G.1
Konig, W.A.2
Rühter, G.3
Stenzel, W.4
Schotten, T.5
-
34
-
-
46549084176
-
Rhodium-catalyzed regioselective arylation of phenylazoles and related compounds with arylboron reagents via C-H bond cleavage
-
10.1016/j.jorganchem.2008.04.029 10.1016/j.jorganchem.2008.04.029 1:CAS:528:DC%2BD1cXnt1OlsL8%3D
-
Miyamura C, Tsurugi H, Satoh T, Miura M (2008) Rhodium-catalyzed regioselective arylation of phenylazoles and related compounds with arylboron reagents via C-H bond cleavage. J Organomet Chem 693:2438-2442. doi: 10.1016/j.jorganchem.2008.04.029
-
(2008)
J Organomet Chem
, vol.693
, pp. 2438-2442
-
-
Miyamura, C.1
Tsurugi, H.2
Satoh, T.3
Miura, M.4
-
35
-
-
84873375156
-
Nucleophilic addition of benzimidazoles to alkynyl bromides/palladium- catalyzed intramolecular C-H vinylation: Synthesis of benzo[4,5]imidazo[2,1-A] isoquinolines
-
10.1021/jo302471z 23272698 10.1021/jo302471z 1:CAS:528:DC%2BC3sXitFCh
-
Peng J, Shang G, Chen C, Miao Z, Li B (2013) Nucleophilic addition of benzimidazoles to alkynyl bromides/palladium-catalyzed intramolecular C-H vinylation: synthesis of benzo[4,5]imidazo[2,1-a]isoquinolines. J Org Chem 78:1242-1248. doi: 10.1021/jo302471z
-
(2013)
J Org Chem
, vol.78
, pp. 1242-1248
-
-
Peng, J.1
Shang, G.2
Chen, C.3
Miao, Z.4
Li, B.5
-
36
-
-
78649676888
-
Novel cyclization of bis-boc-guanidines: Expeditive traceless synthesis of 1,3,5-oxadiazinones under microwave conditions
-
10.1039/c0cc03519j 10.1039/c0cc03519j 1:CAS:528:DC%2BC3cXhsVynurbE
-
Yellol GS, Chung TW, Sun CM (2010) Novel cyclization of bis-boc-guanidines: expeditive traceless synthesis of 1,3,5-oxadiazinones under microwave conditions. Chem Commun 46:9170-9172. doi: 10.1039/c0cc03519j
-
(2010)
Chem Commun
, vol.46
, pp. 9170-9172
-
-
Yellol, G.S.1
Chung, T.W.2
Sun, C.M.3
-
37
-
-
80054725340
-
Base-catalyzed Povarov reaction: An unusual [1,3] sigmatropic rearrangement to dihydropyrimidobenzimidazoles
-
10.1021/ol201985p 21888372 10.1021/ol201985p 1:CAS:528:DC%2BC3MXhtFWjsrvN
-
Chen CH, Yellol GS, Lin PT, Sun CM (2011) Base-catalyzed Povarov reaction: an unusual [1,3] sigmatropic rearrangement to dihydropyrimidobenzimidazoles. Org Lett 13:5120-5123. doi: 10.1021/ol201985p
-
(2011)
Org Lett
, vol.13
, pp. 5120-5123
-
-
Chen, C.H.1
Yellol, G.S.2
Lin, P.T.3
Sun, C.M.4
-
38
-
-
0001608055
-
Trans-(dimethyl sulfoxide-O) (dimethyl sulfoxide-S) bis(trifluoroacetato) palladium(II); Alternative ligation modes of an ambidentate ligand
-
doi: 10.1107/S0108270189001459
-
Bancroft DP, Cotton A, Verbruggen M (1989) Trans-(dimethyl sulfoxide-O) (dimethyl sulfoxide-S) bis(trifluoroacetato)palladium(II); alternative ligation modes of an ambidentate ligand. Acta Crystallogr C 45:1289-1292. doi: 10.1107/S0108270189001459
-
(1989)
Acta Crystallogr C
, vol.45
, pp. 1289-1292
-
-
Bancroft, D.P.1
Cotton, A.2
Verbruggen, M.3
-
39
-
-
84875044854
-
L-shaped benzimidazole fluorophores: Synthesis, characterization and optical response to bases, acids and anions
-
doi: 10.1039/c2cc37120k
-
Lirag RC, Ley HTM, Miljanic OS (2013) L-shaped benzimidazole fluorophores: synthesis, characterization and optical response to bases, acids and anions. Chem Commun 49:4304-4306. doi: 10.1039/c2cc37120k
-
(2013)
Chem Commun
, vol.49
, pp. 4304-4306
-
-
Lirag, R.C.1
Htm, L.2
Miljanic, O.S.3
|