-
1
-
-
0346786657
-
Recent advances in the cross-coupling reactions of organoboron derivatives with organic electrophiles, 1995-1998
-
Suzuki A: Recent advances In the cross-coupling reactions of organoboron derivatives with organic electrophiles, 1995-1998. J Organomet Chem (1999) 576:147-168. •• TOs is an excellent review of the recent literature concerning the Suzuki-Miyaura coupling.
-
(1999)
J Organomet Chem
, vol.576
, pp. 147-168
-
-
Suzuki, A.1
-
2
-
-
0028054343
-
Efficient synthesis of losartan, a nonpeptide angiotensin II receptor antagonist
-
Larsen RD, King AO, Chen CY, Corley EG, Foster BS, Roberts FE, Yang C, Lieberman DR, Reamer RA, Tschaen DM, Verhoeven TR, Reider PJ, Lo YS, Rossano LT, Brookes AS, Meloni D, Moore JR, Amett JF: Efficient synthesis of losartan, a nonpeptide angiotensin II receptor antagonist. J Org Chem (1994) 59:6391-6394.
-
(1994)
J Org Chem
, vol.59
, pp. 6391-6394
-
-
Larsen, R.D.1
King, A.O.2
Chen, C.Y.3
Corley, E.G.4
Foster, B.S.5
Roberts, F.E.6
Yang, C.7
Lieberman, D.R.8
Reamer, R.A.9
Tschaen, D.M.10
Verhoeven, T.R.11
Reider, P.J.12
Lo, Y.S.13
Rossano, L.T.14
Brookes, A.S.15
Meloni, D.16
Moore, J.R.17
Amett, J.F.18
-
3
-
-
0028024461
-
Synthesis of the 5HT1D receptor agonist MK-0462 via a Pd-catalyzed coupling reaction
-
Chen CY, Lieberman DR, Larsen RD, Reamer RA, Verhoeven TR, Reider PJ, Cottrell IF, Houghton PG: Synthesis of the 5HT1D receptor agonist MK-0462 via a Pd-catalyzed coupling reaction. Tetrahedron J.erf (1994) 35:6981-6984.
-
(1994)
Tetrahedron J.erf
, vol.35
, pp. 6981-6984
-
-
Chen, C.Y.1
Lieberman, D.R.2
Larsen, R.D.3
Reamer, R.A.4
Verhoeven, T.R.5
Reider, P.J.6
Cottrell, I.F.7
Houghton, P.G.8
-
4
-
-
0001075641
-
Palladium-catalyzed annulation
-
Larock RC: Palladium-catalyzed annulation. J Organomet Chem (1999) 576:111-124. •• A class of reaction that has had a significant impact on heterocyclic synthesis.
-
(1999)
J Organomet Chem
, vol.576
, pp. 111-124
-
-
Larock, R.C.1
-
5
-
-
0008165462
-
Palladium-catalyzed amlnation of aryl halides and sulfonates
-
Yang BH, Buchwald SL: Palladium-catalyzed amlnation of aryl halides and sulfonates. J Organomet Chem (1999) 576:125-146. •• Important review of the advances in carbon-nitrogen couplings.
-
(1999)
J Organomet Chem
, vol.576
, pp. 125-146
-
-
Yang, B.H.1
Buchwald, S.L.2
-
6
-
-
0000365487
-
-
Yamamoto Y, Negishi (Eds)
-
Yamamoto Y, Negishi (Eds): J Organomet Chem (1999) 576 (1-2):xi-318. ••This issue is a collection of review articles covering many of the active areas of study concerning palladium reactions as a synthetic method.
-
(1999)
J Organomet Chem
, vol.576
, Issue.1-2
-
-
-
7
-
-
33749762244
-
A profile of Professor Richard F Heck: Discovery of the Heck Reaction
-
Negishi E: A profile of Professor Richard F Heck: Discovery of the Heck Reaction. J Organomet Chem (1999) 576:xv-xvi. •• Details one of the true landmark reactions in organic chemistry.
-
(1999)
J Organomet Chem
, vol.576
-
-
Negishi, E.1
-
8
-
-
0032544169
-
Thromboxane modulating agents. 4. Design and synthesis of 3-(2-[((4-chlorophenyl)sulfonyl))-amino]ethylbenzenepropanoic acid derivatives as potent thromboxane receptor antagonists
-
Dack KN, Dickinson RP, Long CJ, Steele J: Thromboxane modulating agents. 4. Design and synthesis of 3-(2-[((4-chlorophenyl)sulfonyl))-amino]ethyl)benzenepropanoic acid derivatives as potent thromboxane receptor antagonists. Bioorg Med Chem Lett (1998) 8:2061-2066.
-
(1998)
Bioorg Med Chem Lett
, vol.8
, pp. 2061-2066
-
-
Dack, K.N.1
Dickinson, R.P.2
Long, C.J.3
Steele, J.4
-
10
-
-
0032577032
-
Total syntheses of (-)-macrolactin A, (+)-macrolactin E, and (-)-macrolactinic acid: An exercise in Stille cross-coupling chemistry
-
Smith III AB, On GR: Total syntheses of (-)-macrolactin A, (+)-macrolactin E, and (-)-macrolactinic acid: an exercise in Stille cross-coupling chemistry. J Am Chem Soc (1998) 120:3935-3948. • This total synthesis demonstrates the impact that palladiumcatalyzed reactions can have on the efficient construction of complex natural products.
-
(1998)
J Am Chem Soc
, vol.120
, pp. 3935-3948
-
-
Smith III, A.B.1
On, G.R.2
-
11
-
-
0001013911
-
A catalytic enantioselective synthesis of the endothelin receptor antagonists SB-209670 and SB-217242. a base-catalyzed stereospecific formal 1,3-hydrogen transfer of a chiral 3arylindenol
-
Clark WM, Tickner-Eldridge AM, Huang GK, Pridgen LN. Olsen MA, Mills RJ. Lantos I, Baine NH: A catalytic enantioselective synthesis of the endothelin receptor antagonists SB-209670 and SB-217242. A base-catalyzed stereospecific formal 1,3-hydrogen transfer of a chiral 3arylindenol. JAm Chem Soc (1998) 120:4550-4551.
-
(1998)
JAm Chem Soc
, vol.120
, pp. 4550-4551
-
-
Clark, W.M.1
Tickner-Eldridge, A.M.2
Huang, G.K.3
Pridgen, L.N.4
Olsen, M.A.5
Mills, R.J.6
Lantos, I.7
Baine, N.H.8
-
12
-
-
0032512011
-
An optimized palladium catalyzed cross-coupling of nonracemic trifluoromethylsulfonyl and fluorosulfonyl enol ethers to arylboronic acids
-
Pridgen LN, Huang GK: An optimized palladium catalyzed cross-coupling of nonracemic trifluoromethylsulfonyl and fluorosulfonyl enol ethers to arylboronic acids. Tetrahedron f.eff (1998) 39:8421-8424.
-
(1998)
Tetrahedron F.eff
, vol.39
, pp. 8421-8424
-
-
Pridgen, L.N.1
Huang, G.K.2
-
13
-
-
0033593964
-
Synthesis and SAR of 2- And 3-substituted 7-azaindoles as potential dopamine D, ligands
-
Curtis NR, Kulagowski JJ, Leeson PD, Ridgill MP, Emms F, Freedman SB, Patel S, Pate) S: Synthesis and SAR of 2- and 3-substituted 7-azaindoles as potential dopamine D, ligands. Bioorg Med Chem Lett (1999) 9:585-588.
-
(1999)
Bioorg Med Chem Lett
, vol.9
, pp. 585-588
-
-
Curtis, N.R.1
Kulagowski, J.J.2
Leeson, P.D.3
Ridgill, M.P.4
Emms, F.5
Freedman, S.B.6
Patel, S.7
Pate, S.8
-
14
-
-
0032560699
-
Synthesis of 5-, 6- and 7-azaindoles via palladium-catalyzed heteroannulation of internal alkynes
-
Ujjainwalla F, Warner D: Synthesis of 5-, 6- and 7-azaindoles via palladium-catalyzed heteroannulation of internal alkynes. Tetrahedron J.e(1998) 39:5355-5358. • The paper is a good adjunct to preparing a variety of azaindoles.
-
(1998)
Tetrahedron J.e
, vol.39
, pp. 5355-5358
-
-
Ujjainwalla, F.1
Warner, D.2
-
15
-
-
0032537692
-
Transition metal catalyzed synthesis of 5-azaindoles
-
Xu L, Lewis IR, Davidsen SK, Summers JB: Transition metal catalyzed synthesis of 5-azaindoles. Tetrahedron J.eft (1998) 39:5159-5162. • The paper is a good adjunct to preparing a variety of azaindoles.
-
(1998)
Tetrahedron J.eft
, vol.39
, pp. 5159-5162
-
-
Xu, L.1
Lewis, I.R.2
Davidsen, S.K.3
Summers, J.B.4
-
16
-
-
0032560237
-
(-)-6-Chloro-2-[(1-furo[2,3c]pyridin-5-ylethyl)thio]-4-pyrimidinamine, PNU-142721, a new broad spectrum HIV-1 non-nucleoside reverse transcriptase inhibitor
-
Wishka DG, Graber DR, Kopta LA, Olmsted RA, Friis JM, Hosley JD, Adams WJ, Seest EP, Castle TM, Dolak LA, Keiser BJ, Yagi Y, Jeganathan A, Schlachter ST, Murphy MJ, Cleek GJ, Nugent RA, Poppe SM, Swaney SM, Man F, Watt W, White WL, Poel TJ, Thomas RC, Voorman RL, Stefanski KJ, Stehle RG, Tarpley WG, Morris J: (-)-6-Chloro-2-[(1-furo[2,3c]pyridin-5-ylethyl)thio]-4-pyrimidinamine, PNU-142721, a new broad spectrum HIV-1 non-nucleoside reverse transcriptase inhibitor. J Med Chem (1998) 41:1357-1360.
-
(1998)
J Med Chem
, vol.41
, pp. 1357-1360
-
-
Wishka, D.G.1
Graber, D.R.2
Kopta, L.A.3
Olmsted, R.A.4
Friis, J.M.5
Hosley, J.D.6
Adams, W.J.7
Seest, E.P.8
Castle, T.M.9
Dolak, L.A.10
Keiser, B.J.11
Yagi, Y.12
Jeganathan, A.13
Schlachter, S.T.14
Murphy, M.J.15
Cleek, G.J.16
Nugent, R.A.17
Poppe, S.M.18
Swaney, S.M.19
Man, F.20
Watt, W.21
White, W.L.22
Poel, T.J.23
Thomas, R.C.24
Voorman, R.L.25
Stefanski, K.J.26
Stehle, R.G.27
Tarpley, W.G.28
Morris, J.29
more..
-
17
-
-
0032582599
-
Stereoselective synthesis of furo[2,3-c]pyridine pyrimidine thioethers, a new class of potent HIV-1 nonnucleoside reverse transcriptase Inhibitors
-
Wishka DG, Graber DR, Seest EP, Dolak LA, Han F, Watt W, Morris J: Stereoselective synthesis of furo[2,3-c]pyridine pyrimidine thioethers, a new class of potent HIV-1 nonnucleoside reverse transcriptase Inhibitors. J Org Chem (1998)63:7851-7859.
-
(1998)
J Org Chem
, vol.63
, pp. 7851-7859
-
-
Wishka, D.G.1
Graber, D.R.2
Seest, E.P.3
Dolak, L.A.4
Han, F.5
Watt, W.6
Morris, J.7
-
18
-
-
0032079256
-
Practical application of the palladiumcatalyzed amination in phenylpiperazine synthesis: An efficient synthesis of a metabolite of the antipsychotic agent aripiprazole
-
Morita S, Kitano K, Matsubara J, Ohtani T, Kawano Y, Otsubo K, Uchida M: Practical application of the palladiumcatalyzed amination in phenylpiperazine synthesis: an efficient synthesis of a metabolite of the antipsychotic agent aripiprazole. Tetrahedron (1998) 54:4811-4818.
-
(1998)
Tetrahedron
, vol.54
, pp. 4811-4818
-
-
Morita, S.1
Kitano, K.2
Matsubara, J.3
Ohtani, T.4
Kawano, Y.5
Otsubo, K.6
Uchida, M.7
-
20
-
-
0032546057
-
Synthesis of cyclopentenyl carbanucleosides via palladium(O) catalysed reactions
-
Kapeller H, Marschner C, Weissenbacher M, Griengl H: Synthesis of cyclopentenyl carbanucleosides via palladium(O) catalysed reactions. Tetrahedron (1998) 54:1439-1456.
-
(1998)
Tetrahedron
, vol.54
, pp. 1439-1456
-
-
Kapeller, H.1
Marschner, C.2
Weissenbacher, M.3
Griengl, H.4
-
21
-
-
33748636953
-
Practical enantiodivergent syntheses of both enantiomers of carbovir, 1592189 and six-membered ring analogues
-
Olivo HF, Yu J: Practical enantiodivergent syntheses of both enantiomers of carbovir, 15921)89 and six-membered ring analogues. J Chem Soc Perkin Trans 1 (1998):391-392.
-
(1998)
J Chem Soc Perkin Trans 1
, pp. 391-392
-
-
Olivo, H.F.1
Yu, J.2
-
22
-
-
0033618139
-
Palladiumcatalyzed C-N bond formation: Facile and general synthesis of A/-aryl 2'-deoxyadenosine analogues
-
Lakshman MK, Keeler JC, Hilmer JH, Martin JQ: Palladiumcatalyzed C-N bond formation: facile and general synthesis of A/-aryl 2'-deoxyadenosine analogues. J Am Chem Soc (1999) 121:6090-6091.
-
(1999)
J Am Chem Soc
, vol.121
, pp. 6090-6091
-
-
Lakshman, M.K.1
Keeler, J.C.2
Hilmer, J.H.3
Martin, J.Q.4
-
24
-
-
0032516312
-
Remarkably selective palladium-catalyzed amination process: Rapid assembly of multiamino based structures
-
Hong Y, Senanayake CH, Xiang T, Vandenbossche CP, Tanoury GJ, Bakale RP, Wald SA: Remarkably selective palladium-catalyzed amination process: rapid assembly of multiamino based structures. Tetrahedron Lett (1998) 39:3121-3124.
-
(1998)
Tetrahedron Lett
, vol.39
, pp. 3121-3124
-
-
Hong, Y.1
Senanayake, C.H.2
Xiang, T.3
Vandenbossche, C.P.4
Tanoury, G.J.5
Bakale, R.P.6
Wald, S.A.7
-
25
-
-
0001688262
-
An improved synthesis of YC-1
-
Gordon DW: An improved synthesis of YC-1. Synlett (1998):1065-1066.
-
(1998)
Synlett
, pp. 1065-1066
-
-
Gordon, D.W.1
-
26
-
-
0033612127
-
Suzuki-type cross-coupling reaction of 3-lodoindazoles with aryl boronic acids: A general and flexible route to 3arylindazoles
-
Collot V, Dallemagne P, Bovy PR, Rault S: Suzuki-type cross-coupling reaction of 3-lodoindazoles with aryl boronic acids: a general and flexible route to 3arylindazoles. Tetrahedron (1999) 55:6917-6922.
-
(1999)
Tetrahedron
, vol.55
, pp. 6917-6922
-
-
Collot, V.1
Dallemagne, P.2
Bovy, P.R.3
Rault, S.4
-
27
-
-
0033538646
-
Synergistic methodologies for the synthesis of 3-aroyl-2arylbenzo[b]thiophene-based selective estrogen receptor modulators. Two concise syntheses of raloxifene
-
Bradley DA, Godfrey AG, Schmid CR: Synergistic methodologies for the synthesis of 3-aroyl-2arylbenzo[b]thiophene-based selective estrogen receptor modulators. Two concise syntheses of raloxifene. Tetrahedron J.eff (1999) 40:5155-5159.
-
(1999)
Tetrahedron J.eff
, vol.40
, pp. 5155-5159
-
-
Bradley, D.A.1
Godfrey, A.G.2
Schmid, C.R.3
-
28
-
-
0033535105
-
Diamino benzo[b]thiophene derivatives as a novel class of active site directed thrombin inhibitors: 3. Enhancing activity by imposing conformational restriction in the C-4" side chain
-
Bastian JA, Chirgadze N, Denney ML, Gifford-Moore DS, Sail DJ, Smith GF, Wikel JH: Diamino benzo[b]thiophene derivatives as a novel class of active site directed thrombin inhibitors: 3. Enhancing activity by imposing conformational restriction in the C-4" side chain. Bioorg Med Chem Lett (1999) 9:363-368.
-
(1999)
Bioorg Med Chem Lett
, vol.9
, pp. 363-368
-
-
Bastian, J.A.1
Chirgadze, N.2
Denney, M.L.3
Gifford-Moore, D.S.4
Sail, D.J.5
Smith, G.F.6
Wikel, J.H.7
-
29
-
-
0033535387
-
Dibasic benzo[b]thiophene derivatives as a novel class of active site directed thrombin inhibitors: 4. SAR studies on the conformationally restricted C-3 side chain of hydroxybenzo[b]thiophenes
-
Takeuchi K, Kohn TJ, Sail DJ, Denney ML, McCowan JR, Smith GF, Gifford-Moore DS: Dibasic benzo[b]thiophene derivatives as a novel class of active site directed thrombin inhibitors: 4. SAR studies on the conformationally restricted C-3 side chain of hydroxybenzo[b]thiophenes. Bioorg Med Chem Lett (1999)9:759-764.
-
(1999)
Bioorg Med Chem Lett
, vol.9
, pp. 759-764
-
-
Takeuchi, K.1
Kohn, T.J.2
Sail, D.J.3
Denney, M.L.4
McCowan, J.R.5
Smith, G.F.6
Gifford-Moore, D.S.7
-
31
-
-
7344236839
-
Practical synthesis of antimethicillin-resistant staphylococcus aureus (MRS A) carbapenem L-742,728
-
Yasuda N, Huffman MA, Ho GJ, Xavier LC, Yang C, Emerson KM, Tsay FR, Li Y, Kress MH, Rieger DL, Karady S, Sohar P, Abramson NL, DeCamp AE, Mathre DJ, Douglas AW, Dolling UH, Grabowski EJ, Reider PJ: Practical synthesis of antimethicillin-resistant staphylococcus aureus (MRS A) carbapenem L-742,728. J Org Chem (1998) 63:5438-5446.
-
(1998)
J Org Chem
, vol.63
, pp. 5438-5446
-
-
Yasuda, N.1
Huffman, M.A.2
Ho, G.J.3
Xavier, L.C.4
Yang, C.5
Emerson, K.M.6
Tsay, F.R.7
Li, Y.8
Kress, M.H.9
Rieger, D.L.10
Karady, S.11
Sohar, P.12
Abramson, N.L.13
DeCamp, A.E.14
Mathre, D.J.15
Douglas, A.W.16
Dolling, U.H.17
Grabowski, E.J.18
Reider, P.J.19
-
32
-
-
0033556115
-
Preparation of crystalline p-nitrobenzyl 2-hydroxymethyl carbapenem as a key Intermediate for the anti-MHS carbapenem L-786,392
-
Yasuda N, Yang C, Wells KM, Jensen MS, Hughes DL: Preparation of crystalline p-nitrobenzyl 2-hydroxymethyl carbapenem as a key Intermediate for the anti-MHS carbapenem L-786,392. Tetrahedron Lett (1999) 40:427-430.
-
(1999)
Tetrahedron Lett
, vol.40
, pp. 427-430
-
-
Yasuda, N.1
Yang, C.2
Wells, K.M.3
Jensen, M.S.4
Hughes, D.L.5
-
33
-
-
0032473902
-
The syntheses of functionalized 2-alkenyl and alkynyl-1-/J-methyl-carbapenems via the Stille cross-coupling reaction
-
Dykstra KD, DiNinno F: The syntheses of functionalized 2-alkenyl and alkynyl-1-/J-methyl-carbapenems via the Stille cross-coupling reaction. Tetrahedron Lett (1998) 39:1865-1868.
-
(1998)
Tetrahedron Lett
, vol.39
, pp. 1865-1868
-
-
Dykstra, K.D.1
DiNinno, F.2
-
34
-
-
0033547956
-
Stille coupling approaches to the stereospecific synthesis of 7-[(£)-alkyIidene]cephalosporins
-
Buynak JD, Doppalapudi VR, Frotan M, Kumar R: Stille coupling approaches to the stereospecific synthesis of 7-[(£)-alkyIidene]cephalosporins. Tetrahedron Lett (1999) 40:1281-1284.
-
(1999)
Tetrahedron Lett
, vol.40
, pp. 1281-1284
-
-
Buynak, J.D.1
Doppalapudi, V.R.2
Frotan, M.3
Kumar, R.4
-
35
-
-
0032549047
-
A practical and .efficient synthesis of the selective neuronal acetylcholine-gated ion channel agonist (S)-(-)-5-ethynyl-3-(1 -methyl-2-pyrrolidinyl)pyridine maleate (SIB-1508Y)
-
Bleicher LS, Cosford NDP, Herbaut A, McCallum JS, McDonald IA: A practical and .efficient synthesis of the selective neuronal acetylcholine-gated ion channel agonist (S)-(-)-5-ethynyl-3-(1 -methyl-2-pyrrolidinyl)pyridine maleate (SIB-1508Y). J Org Chem (1998) 63:1109-1118.
-
(1998)
J Org Chem
, vol.63
, pp. 1109-1118
-
-
Bleicher, L.S.1
Cosford, N.D.P.2
Herbaut, A.3
McCallum, J.S.4
McDonald, I.A.5
-
36
-
-
0032491270
-
2-Pyridinyl-3-(4-methylsulfonyl)phenylpyridines: Selective and orally active cyclooxygenase-2 inhibitors
-
Friesen RW, Brideau C, Chan CG, Charleson S, Deschenes D, Dube D, Ethier D, Fortin R, Gauthier JY, Girard Y, Gordon R, Greig GM, Riendeau D, Savoie C, Wang Z, Wong E, Visco D, Xu U, Young RN: 2-Pyridinyl-3-(4-methylsulfonyl)phenylpyridines: selective and orally active cyclooxygenase-2 inhibitors. Bioorg Med Chem Lett (1998) 8:2777-2782.
-
(1998)
Bioorg Med Chem Lett
, vol.8
, pp. 2777-2782
-
-
Friesen, R.W.1
Brideau, C.2
Chan, C.G.3
Charleson, S.4
Deschenes, D.5
Dube, D.6
Ethier, D.7
Fortin, R.8
Gauthier, J.Y.9
Girard, Y.10
Gordon, R.11
Greig, G.M.12
Riendeau, D.13
Savoie, C.14
Wang, Z.15
Wong, E.16
Visco, D.17
Xu, U.18
Young, R.N.19
-
37
-
-
0033591643
-
2Heterosubstituted-3-(4-methylsulfonyl)phenyl-5-trifluoromethyl pyridines as selective and orally active cyclooxygenase-2 inhibitors
-
Dube D, Brideau C, Deschenes D, Fortin R, Friesen RW, Gordon R, Girard Y, Riendeau D, Savoie C, Chan CC: 2Heterosubstituted-3-(4-methylsulfonyl)phenyl-5-trifluoromethyl pyridines as selective and orally active cyclooxygenase-2 inhibitors. Bioorg Med Chem Lett (1999) 9:1715-1720.
-
(1999)
Bioorg Med Chem Lett
, vol.9
, pp. 1715-1720
-
-
Dube, D.1
Brideau, C.2
Deschenes, D.3
Fortin, R.4
Friesen, R.W.5
Gordon, R.6
Girard, Y.7
Riendeau, D.8
Savoie, C.9
Chan, C.C.10
-
38
-
-
0033526093
-
Terphenyl cyclooxygenase-2 (COX-2) inhibitors: Optimization of the central ring and o-biphenyl analogs
-
Pinto DJP, Ball DG, Pitts WJ, Petraitis JJ, Orwat MJ, Wang S, Jetter JW, Sherk SR, Houghton GC, Copeland RA, Covington MB, Trzaskos JM, Magolda RL: Terphenyl cyclooxygenase-2 (COX-2) inhibitors: optimization of the central ring and o-biphenyl analogs. Bioorg Med Chem Lett (1999) 9:919-924.
-
(1999)
Bioorg Med Chem Lett
, vol.9
, pp. 919-924
-
-
Pinto, D.J.P.1
Ball, D.G.2
Pitts, W.J.3
Petraitis, J.J.4
Orwat, M.J.5
Wang, S.6
Jetter, J.W.7
Sherk, S.R.8
Houghton, G.C.9
Copeland, R.A.10
Covington, M.B.11
Trzaskos, J.M.12
Magolda, R.L.13
-
39
-
-
0033574589
-
Synthesis of 3-carboxy-20-keto steroid, SB 209963, a 5a-reductase inhibitor, by palladiumcatalyzed hydroxycarbonylation
-
Yu MS, Baine NH: Synthesis of 3-carboxy-20-keto steroid, SB 209963, a 5a-reductase inhibitor, by palladiumcatalyzed hydroxycarbonylation. Tetrahedron Left (1999) 40: 3123-3124.
-
(1999)
Tetrahedron Left
, vol.40
, pp. 3123-3124
-
-
Yu, M.S.1
Baine, N.H.2
-
40
-
-
0031978238
-
Palladium and nickel catalyzed hydroxycarbonylation of a steroidal bromodiene in the synthesis of episteride, a potent 5orreductase inhibitor
-
McGuire, MA, Sorenson E, Klein DN, Baine NH: Palladium and nickel catalyzed hydroxycarbonylation of a steroidal bromodiene in the synthesis of episteride, a potent 5orreductase inhibitor. Synth Commun (1998) 28:1611-1615.
-
(1998)
Synth Commun
, vol.28
, pp. 1611-1615
-
-
McGuire, M.A.1
Sorenson, E.2
Klein, D.N.3
Baine, N.H.4
-
41
-
-
0032537093
-
Preparation of indole-2carboxamides by palladium-catalysed carbonylation
-
Herbert JM, McNeill AH: Preparation of indole-2carboxamides by palladium-catalysed carbonylation.Tetrahedron Lett (1998) 39:2421-2424.
-
(1998)
Tetrahedron Lett
, vol.39
, pp. 2421-2424
-
-
Herbert, J.M.1
McNeill, A.H.2
-
42
-
-
0033518569
-
An approach to the synthesis of CP263,114: A remarkably facile silyloxy-Cope rearrangement
-
Bio MM, Leighton JL: An approach to the synthesis of CP263,114: a remarkably facile silyloxy-Cope rearrangement J Am Chem Soc(1999) 121:890-891.
-
(1999)
J Am Chem Soc
, vol.121
, pp. 890-891
-
-
Bio, M.M.1
Leighton, J.L.2
-
43
-
-
7844232968
-
W-(2-Benzoylphenyl)-Ltyrosine PPARy agonists. 3. Structure-activity relationship and optimization of the W-aryl substituent
-
Cobb JE, Blanchard SG, Boswell EG, Brown KK, Charifson PS, Cooper JP, Collins JL, Dezube M, Henke BR, Hull-Ryde EA, Lake DH, Lenhard JM, Oliver, Jr W, Oplinger J, Pentti M, Parks DJ, Plunket KD, Tong WQ: W-(2-Benzoylphenyl)-Ltyrosine PPARy agonists. 3. Structure-activity relationship and optimization of the W-aryl substituent. J Med Chem (1998)41:5055-5069.
-
(1998)
J Med Chem
, vol.41
, pp. 5055-5069
-
-
Cobb, J.E.1
Blanchard, S.G.2
Boswell, E.G.3
Brown, K.K.4
Charifson, P.S.5
Cooper, J.P.6
Collins, J.L.7
Dezube, M.8
Henke, B.R.9
Hull-Ryde, E.A.10
Lake, D.H.11
Lenhard, J.M.12
Oliver Jr., W.13
Oplinger, J.14
Pentti, M.15
Parks, D.J.16
Plunket, K.D.17
Tong, W.Q.18
-
44
-
-
33749724415
-
Epibatidine
-
Epibatidine. Drugs Future (1998) 23:1243.
-
(1998)
Drugs Future
, vol.23
, pp. 1243
-
-
-
45
-
-
0032998103
-
Asymmetric synthesis of both enantiomers of /V-protected epibatidine via reductive Hecktype hetarylation
-
Namyslo JC, Kaufmann DE: Asymmetric synthesis of both enantiomers of /V-protected epibatidine via reductive Hecktype hetarylation. Synlett (1999):804-806.
-
(1999)
Synlett
, pp. 804-806
-
-
Namyslo, J.C.1
Kaufmann, D.E.2
-
46
-
-
0032934387
-
Chemistry in the ambient field of the alkaloid epibatidine 2: Triphenylarsine as an efficient ligand in the Pd-catalyzed synthesis of epibatidine and analogs
-
Namyslo JC, Kaufmann DE: Chemistry in the ambient field of the alkaloid epibatidine 2: triphenylarsine as an efficient ligand in the Pd-catalyzed synthesis of epibatidine and analogs. Synteff(1999):114-116.
-
(1999)
Synteff
, pp. 114-116
-
-
Namyslo, J.C.1
Kaufmann, D.E.2
-
47
-
-
0032771261
-
Huperzine A: A novel acetylcholinesterase inhibitor
-
Tang XC, He XC, Bai DL: Huperzine A: a novel acetylcholinesterase inhibitor. Drugs Future (1999) 24:647-663.
-
(1999)
Drugs Future
, vol.24
, pp. 647-663
-
-
Tang, X.C.1
He, X.C.2
Bai, D.L.3
-
48
-
-
0032474510
-
Synthesis and anticholinesterase activity of huperzine a analogues containing phenol and catechol replacements for the pyridone ring
-
Campiani G, Kozikowski AP, Wang S, Ming L, Nacci V, Saxena A, Doctor BP: Synthesis and anticholinesterase activity of huperzine A analogues containing phenol and catechol replacements for the pyridone ring. Bioorg Med Chem Lett (1998)8:1413-1418.
-
(1998)
Bioorg Med Chem Lett
, vol.8
, pp. 1413-1418
-
-
Campiani, G.1
Kozikowski, A.P.2
Wang, S.3
Ming, L.4
Nacci, V.5
Saxena, A.6
Doctor, B.P.7
-
49
-
-
0032576817
-
Studies on asymmetric synthesis of huperzine A. 1. Palladium-catalyzed asymmetric bicycloannulation of 5,6,7,8-tetrahydro-2-methoxy-6-oxo-5quinolinecarboxylic esters
-
He XC, Wang B, Bai D: Studies on asymmetric synthesis of huperzine A. 1. Palladium-catalyzed asymmetric bicycloannulation of 5,6,7,8-tetrahydro-2-methoxy-6-oxo-5quinolinecarboxylic esters. Tetrahedron Lett (1998) 39:411414.
-
(1998)
Tetrahedron Lett
, vol.39
, pp. 411414
-
-
He, X.C.1
Wang, B.2
Bai, D.3
-
50
-
-
0033553112
-
Palladium-catalyzed kinetic and dynamic kinetic asymmetric transformation of 5-acyloxy-2(5H)-furanone. Enantioselective synthesis of (-)-aflatoxin B lactone
-
Trost BM, Toste FD: Palladium-catalyzed kinetic and dynamic kinetic asymmetric transformation of 5-acyloxy-2(5H)-furanone. Enantioselective synthesis of (-)-aflatoxin B lactone. JAm Chem Soc(1999) 121:3543-3544. • An excellent example of the role palladium reactions can play as a linchpin in the synthesis of medicinal agents and natural products.
-
(1999)
JAm Chem Soc
, vol.121
, pp. 3543-3544
-
-
Trost, B.M.1
Toste, F.D.2
-
51
-
-
0039835147
-
Recent progress in solid phase heterocycle syntheses. a review
-
Corbett JW: Recent progress in solid phase heterocycle syntheses. A review. Org Prep Proc Int (1998) 30:489-550.
-
(1998)
Org Prep Proc Int
, vol.30
, pp. 489-550
-
-
Corbett, J.W.1
-
52
-
-
33646449394
-
Carbon-carbon bond forming solidphase reactions
-
Lorsbach BA, Kurth MJ: Carbon-carbon bond forming solidphase reactions. Chem Rev(1999) 99:1549-1581.
-
(1999)
Chem Rev
, vol.99
, pp. 1549-1581
-
-
Lorsbach, B.A.1
Kurth, M.J.2
-
53
-
-
0032564639
-
Solid-phase synthesis of heterocycles via palladium-catalyzed annulation
-
Wang Y, Huang TN: Solid-phase synthesis of heterocycles via palladium-catalyzed annulation. Tetrahedron Lett (1998) 39:9605-9608.
-
(1998)
Tetrahedron Lett
, vol.39
, pp. 9605-9608
-
-
Wang, Y.1
Huang, T.N.2
-
54
-
-
0032478678
-
Solid-phase synthesis of diverse E- And F-series prostaglandins
-
Thompson LA, Moore FL, Moon YC, Ellman JA: Solid-phase synthesis of diverse E- and F-series prostaglandins. J Org Chem (1998) 63:2066-2067. • Example of how palladium catalysis can assist in building diversity in complex medicinal agents.
-
(1998)
J Org Chem
, vol.63
, pp. 2066-2067
-
-
Thompson, L.A.1
Moore, F.L.2
Moon, Y.C.3
Ellman, J.A.4
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