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Volumn 2, Issue 6, 1999, Pages 651-667

Palladium catalysis in the synthesis of medicinal agents

Author keywords

Asymmetric synthesis; Carbon carbon coupling; Carbon nitrogen bond formation; Carbonylation; Heterocycles; Palladium catalysis

Indexed keywords

1 BENZYL 3 (5 HYDROXYMETHYL 2 FURYL)INDAZOLE; 3 (2 CARBOXYMETHOXY 4 METHOXYPHENYL) 1 (3,4 METHYLENEDIOXYPHENYL) 5 PROPOXY 2 INDANCARBOXYLIC ACID; 3 [[4 (4 CHLOROPHENYL) 1 PIPERAZINYL]METHYL] 1H PYRROLO[2,3 B]PYRIDINE; 3 ETHYNYL 5 (1 METHYL 2 PYRROLIDINYL)PYRIDINE; 4 [2 [5,6 DIHYDRO 5,5 DIMETHYL 8 (4 METHYLPHENYL) 2 NAPHTHYL]ETHYNYL]BENZOIC ACID; 6 CHLORO 2 [(1 FURO[2,3 C]PYRIDIN 5 YLETHYL)THIO] 4 PYRIMIDINAMINE; ABACAVIR; ANTIPARKINSON AGENT; ARIPIPRAZOLE; ARZOXIFENE; BENZOTHIOPHENE; CARBAPENEM; CARBOVIR; CEPHALOSPORIN DERIVATIVE; CYCLOOXYGENASE 2 INHIBITOR; ENRASENTAN; EPRISTERIDE; L 742728; L 786392; LINTITRIPT; NORASTEMIZOLE; OXIDOREDUCTASE INHIBITOR; PALLADIUM; RALOXIFENE; RNA DIRECTED DNA POLYMERASE INHIBITOR; SB 209953; THROMBIN INHIBITOR; THROMBOXANE RECEPTOR AFFECTING AGENT; UK 147535; UNCLASSIFIED DRUG; UNINDEXED DRUG;

EID: 0032735203     PISSN: 13676733     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review
Times cited : (14)

References (54)
  • 1
    • 0346786657 scopus 로고    scopus 로고
    • 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
  • 4
    • 0001075641 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 14
    • 0032560699 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 17
    • 0032582599 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 25
    • 0001688262 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 32
    • 0033556115 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 39
    • 0033574589 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 44
    • 33749724415 scopus 로고    scopus 로고
    • Epibatidine
    • Epibatidine. Drugs Future (1998) 23:1243.
    • (1998) Drugs Future , vol.23 , pp. 1243
  • 45
    • 0032998103 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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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