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Volumn 6, Issue 6, 2003, Pages 930-944

Progress toward the synthesis of hinckdentine A

Author keywords

Bryozoan natural product; Hinckdentine A; Indolo 1,2 c quinazoline; Marine alkaloid; Rearrangement; Synthesis

Indexed keywords

11B,12,13,14,15,16 HEXAHYDROAZEPINO[4',5':2,3]INDOLO[1,2 C]QUINAZOLINE; 4A METHYL 1,2,3,4 TETRAHYDRO 4AH CARBAZOLE; CARBAZOLE DERIVATIVE; HINCKDENTINE A; HINCKSINOFLUSTRA DENTICULATE EXTRACT; INDOLE DERIVATIVE; INDOLO[1,2 C]QUINAZOLINE DERIVATIVE; ORGANOLITHIUM COMPOUND; QUINAZOLINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0346458785     PISSN: 13676733     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review
Times cited : (3)

References (48)
  • 1
    • 0000514534 scopus 로고
    • Hinckdentine-A: A novel alkaloid from the marine bryozoan Hincksinoflustra denticulata
    • Blackman AJ, Hambly TW, Picker, K, Taylor WC, Thirasasana N: Hinckdentine-A: A novel alkaloid from the marine bryozoan Hincksinoflustra denticulata. Tetrahedron Lett (1987) 28(45):5561-5562. The isolation and structural characterization of hinckdentine A.
    • (1987) Tetrahedron Lett , vol.28 , Issue.45 , pp. 5561-5562
    • Blackman, A.J.1    Hambly, T.W.2    Picker, K.3    Taylor, W.C.4    Thirasasana, N.5
  • 2
    • 33750219084 scopus 로고
    • Bryozoan secondary metabolites and their chemical ecology
    • Atta-ur-Rahman (Ed), Elsevier, Amsterdam, the Netherlands
    • Blackman AJ, Walls, JT: Bryozoan secondary metabolites and their chemical ecology. In: Studies in Natural Products Chemistry, Structure and Chemistry Part D. Atta-ur-Rahman (Ed), Elsevier, Amsterdam, the Netherlands (1995):73-112. A review of the known bryozoan secondary metabolites and a discussion of their chemical ecology.
    • (1995) Studies in Natural Products Chemistry, Structure and Chemistry Part D , pp. 73-112
    • Blackman, A.J.1    Walls, J.T.2
  • 3
    • 0000354013 scopus 로고    scopus 로고
    • Indoloquinazolines: A century in review
    • Billimoria AD, Cava MP: Indoloquinazolines: A century in review. Heterocycles (1996) 42(1):453-473. A comprehensive review of the chemistry of indoloquinazolines.
    • (1996) Heterocycles , vol.42 , Issue.1 , pp. 453-473
    • Billimoria, A.D.1    Cava, M.P.2
  • 4
    • 0242528072 scopus 로고
    • The action of acyl cyanides on 2- and 1:2-substituted indoles. Part II. Derivatives of 2-o-aminophenylindole
    • Kiang AK, Mann FG, Prior AF, Topham A: The action of acyl cyanides on 2- and 1:2-substituted indoles. Part II. Derivatives of 2-o-aminophenylindole. J Chem Soc (1956):1319-1331.
    • (1956) J Chem Soc , pp. 1319-1331
    • Kiang, A.K.1    Mann, F.G.2    Prior, A.F.3    Topham, A.4
  • 5
    • 84982066556 scopus 로고
    • Indoles and isatogens. XIX. Rearrangement of o-amino tolans or stilbenes into derivatives of indole or indoline
    • Ruggli P, Schmid, O: Indoles and isatogens. XIX. Rearrangement of o-amino tolans or stilbenes into derivatives of indole or indoline. Helv Chim Acta (1935) 18:1215-1228.
    • (1935) Helv Chim Acta , vol.18 , pp. 1215-1228
    • Ruggli, P.1    Schmid, O.2
  • 6
    • 0002082317 scopus 로고
    • Indoles, benzofurans, phthalides, and tolanes via copper(I) acetylides
    • Castro CE, Gaughan EJ, Owsley DC: Indoles, benzofurans, phthalides, and tolanes via copper(I) acetylides. J Org Chem (1966) 31(12):4071-4078.
    • (1966) J Org Chem , vol.31 , Issue.12 , pp. 4071-4078
    • Castro, C.E.1    Gaughan, E.J.2    Owsley, D.C.3
  • 7
    • 0000056092 scopus 로고
    • Thallium in organic synthesis. 68. A convenient synthesis of 2-phenylindoles from anilides
    • Taylor EC, Katz AH, McKillop HS: Thallium in organic synthesis. 68. A convenient synthesis of 2-phenylindoles from anilides. Tetrahedron Lett (1985) 26(48):5963-5966.
    • (1985) Tetrahedron Lett , vol.26 , Issue.48 , pp. 5963-5966
    • Taylor, E.C.1    Katz, A.H.2    McKillop, H.S.3
  • 8
    • 0002103980 scopus 로고
    • Facile synthesis of 2-substituted indoles from o-bromoaniline
    • Sakamoto T, Kondo Y, Yamanaka H: Facile synthesis of 2-substituted indoles from o-bromoaniline. Heterocycles (1986) 24(1):31-32.
    • (1986) Heterocycles , vol.24 , Issue.1 , pp. 31-32
    • Sakamoto, T.1    Kondo, Y.2    Yamanaka, H.3
  • 9
    • 0034815684 scopus 로고    scopus 로고
    • Indole[1,2-c]quinazolines by palladium-catalyzed cyclization of bis(o-trifluoroacetamidophenyl) acetylene with aryl and vinyl halides or triflates
    • Arcadi A, Cacchi S, Cassetta A, Fabrizi G, Parisi LM: Indole[1,2-c]quinazolines by palladium-catalyzed cyclization of bis(o-trifluoroacetamidophenyl) acetylene with aryl and vinyl halides or triflates. Synlett (2001) (10):1605-1607.
    • (2001) Synlett , Issue.10 , pp. 1605-1607
    • Arcadi, A.1    Cacchi, S.2    Cassetta, A.3    Fabrizi, G.4    Parisi, L.M.5
  • 10
    • 0037129385 scopus 로고    scopus 로고
    • 12-Acylindolo[1,2-c]quinazolines by palladium-catalyzed cyclocarbonylation of o-alkylnyltrifluoroacetanilides
    • Battistuzzi G, Cacchi S, Fabrizi G, Marinelli F, Parisi LM: 12-Acylindolo[1,2-c]quinazolines by palladium-catalyzed cyclocarbonylation of o-alkylnyltrifluoroacetanilides. Org Lett (2002) 4(8):1355-1358.
    • (2002) Org Lett , vol.4 , Issue.8 , pp. 1355-1358
    • Battistuzzi, G.1    Cacchi, S.2    Fabrizi, G.3    Marinelli, F.4    Parisi, L.M.5
  • 11
    • 0034679471 scopus 로고    scopus 로고
    • Versatile indole synthesis by a 5-endo-dig cyclization mediated by potassium or cesium bases
    • Rodriguez AL, Koradin C, Dohle W, Knochel P: Versatile indole synthesis by a 5-endo-dig cyclization mediated by potassium or cesium bases. Angew Chem Int Ed (2000) 39(14):2488-2490.
    • (2000) Angew Chem Int Ed , vol.39 , Issue.14 , pp. 2488-2490
    • Rodriguez, A.L.1    Koradin, C.2    Dohle, W.3    Knochel, P.4
  • 12
    • 0037463514 scopus 로고    scopus 로고
    • Synthesis of polyfunctional indoles and related heterocycles mediated by cesium and potassium bases
    • Koradin C, Dohle W, Rodriguez AL, Schmid B, Knochel P: Synthesis of polyfunctional indoles and related heterocycles mediated by cesium and potassium bases. Tetrahedron (2003) 59(9):1571-1587. A novel synthesis of the tribrominated 2-(2-aminophenyl)indole.
    • (2003) Tetrahedron , vol.59 , Issue.9 , pp. 1571-1587
    • Koradin, C.1    Dohle, W.2    Rodriguez, A.L.3    Schmid, B.4    Knochel, P.5
  • 13
    • 0034687205 scopus 로고    scopus 로고
    • Reaction of 2-bromomethylazoles and TosMIC: A domino process to azolopyrimidines. Synthesis of core tricycle of the variolins alkaloids
    • Mendiola J, Minguez JM, Alvarez-Builla J, Vaquero JJ: Reaction of 2-bromomethylazoles and TosMIC: A domino process to azolopyrimidines. Synthesis of core tricycle of the variolins alkaloids. Org Lett (2000) 2(21):3253-3256.
    • (2000) Org Lett , vol.2 , Issue.21 , pp. 3253-3256
    • Mendiola, J.1    Minguez, J.M.2    Alvarez-Builla, J.3    Vaquero, J.J.4
  • 14
    • 0037415489 scopus 로고    scopus 로고
    • Novel 6-substituted benzothiazol-2-yl indolo[1,2-c]quinazolines and benzimidazo[1,2-c]-quinazolines
    • Frère S, Thiéry V, Bailly C, Besson T: Novel 6-substituted benzothiazol-2-yl indolo[1,2-c]quinazolines and benzimidazo[1,2-c]-quinazolines. Tetrahedron (2003) 59(6):773-779.
    • (2003) Tetrahedron , vol.59 , Issue.6 , pp. 773-779
    • Frère, S.1    Thiéry, V.2    Bailly, C.3    Besson, T.4
  • 15
    • 0035903950 scopus 로고    scopus 로고
    • Efficient modified von Niementowski synthesis of novel derivatives of 5a,14b,15-triazabenzo[a]indeno[1,2-c]anthracen-5-one from indolo[1,2-c]quinazoline
    • Domon L, Le Coeur C, Grelard A, Thiéry V, Besson T: Efficient modified von Niementowski synthesis of novel derivatives of 5a,14b,15-triazabenzo[a]indeno[1,2-c]anthracen-5-one from indolo[1,2-c]quinazoline. Tetrahedron Lett (2001) 42(38):6671-6674.
    • (2001) Tetrahedron Lett , vol.42 , Issue.38 , pp. 6671-6674
    • Domon, L.1    Le Coeur, C.2    Grelard, A.3    Thiéry, V.4    Besson, T.5
  • 16
    • 0037193113 scopus 로고    scopus 로고
    • Vinyl vicinal tricarbonyl esters as trielectrophiles. Reaction with diamines and related trinucleophiles
    • Wasserman HH, Long YO, Zhang R, Carr AJ, Parr J: Vinyl vicinal tricarbonyl esters as trielectrophiles. Reaction with diamines and related trinucleophiles. Tetrahedron Lett (2002) 43(18):3347-3350.
    • (2002) Tetrahedron Lett , vol.43 , Issue.18 , pp. 3347-3350
    • Wasserman, H.H.1    Long, Y.O.2    Zhang, R.3    Carr, A.J.4    Parr, J.5
  • 17
    • 0029750203 scopus 로고    scopus 로고
    • 2,3-Dihydro-2-carboxy-1H-inclol-3-Essigsäuren als Sonden zur Untersuchung exzitatorischer Aminosäurerezeptoren
    • Noe CR, Knollmüller M, Schodl C, Berger ML: 2,3-Dihydro-2-carboxy-1H-inclol-3-Essigsäuren als Sonden zur Untersuchung exzitatorischer Aminosäurerezeptoren. Sci Pharm (1996) 64(3-4):577-590.
    • (1996) Sci Pharm , vol.64 , Issue.3-4 , pp. 577-590
    • Noe, C.R.1    Knollmüller, M.2    Schodl, C.3    Berger, M.L.4
  • 18
    • 0242475033 scopus 로고
    • The structure of the so-called 11-hydrotetrahydrocarbazolenine
    • Witkop B: The structure of the so-called 11-hydrotetrahydrocarbazolenine. J Am Chem Soc (1950) 72(1):614-620.
    • (1950) J Am Chem Soc , vol.72 , Issue.1 , pp. 614-620
    • Witkop, B.1
  • 19
    • 0242643445 scopus 로고
    • Rearrangements and revisions in the tetrahydrocarbazole series
    • Patrick JB, Witkop B: Rearrangements and revisions in the tetrahydrocarbazole series. J Am Chem Soc (1950) 72(1):633-634. The first observation of the pinacol-like rearrangement of a 3H-indol-3-ol to an indolin-3-one.
    • (1950) J Am Chem Soc , vol.72 , Issue.1 , pp. 633-634
    • Patrick, J.B.1    Witkop, B.2
  • 20
    • 0001150248 scopus 로고
    • Stereospecific total synthesis of dl-austamide
    • Hutchison AJ, Kishi Y: Stereospecific total synthesis of dl-austamide. J Am Chem Soc (1979) 101(22):6786-6788. The first application of the pinacol-like rearrangement of a 3H-indol-3-ol to an indolin-3-one in natural products synthesis.
    • (1979) J Am Chem Soc , vol.101 , Issue.22 , pp. 6786-6788
    • Hutchison, A.J.1    Kishi, Y.2
  • 21
    • 0025357644 scopus 로고
    • Asymmetric, stereocontrolled total synthesis of (-)-brevianamide B
    • Williams RM, Glinka T, Kwast E, Coffman H, Stille JK: Asymmetric, stereocontrolled total synthesis of (-)-brevianamide B. J Am Chem Soc (1990) 112(2):808-821.
    • (1990) J Am Chem Soc , vol.112 , Issue.2 , pp. 808-821
    • Williams, R.M.1    Glinka, T.2    Kwast, E.3    Coffman, H.4    Stille, J.K.5
  • 22
    • 0027401143 scopus 로고
    • Total synthesis of (-)-alloaristoteline, (-)-serratoline, and (+)-aristotelone
    • Stoermer D, Heathcock CH: Total synthesis of (-)-alloaristoteline, (-)-serratoline, and (+)-aristotelone. J Org Chem (1993) 58(3):564-568.
    • (1993) J Org Chem , vol.58 , Issue.3 , pp. 564-568
    • Stoermer, D.1    Heathcock, C.H.2
  • 23
    • 0028604444 scopus 로고
    • Synthesis of aristotelia-type alkaloids. Part XIII. Total syntheses of (+)-makonine, (+)-aristotelinone, and (+)-11,12-didehydroaristoteline
    • Stahl R, Galli R, Güller R, Borschberg HJ: Synthesis of aristotelia-type alkaloids. Part XIII. Total syntheses of (+)-makonine, (+)-aristotelinone, and (+)-11,12-didehydroaristoteline. Helv Chim Acta (1994) 77(8):2125-2132.
    • (1994) Helv Chim Acta , vol.77 , Issue.8 , pp. 2125-2132
    • Stahl, R.1    Galli, R.2    Güller, R.3    Borschberg, H.J.4
  • 24
    • 84987344380 scopus 로고
    • 3H-Indol-3-ols by a novel ring contraction
    • Lednicer D, Emmert DE: 3H-Indol-3-ols by a novel ring contraction. J Heterocyclic Chem (1970) 7(3):575-581.
    • (1970) J Heterocyclic Chem , vol.7 , Issue.3 , pp. 575-581
    • Lednicer, D.1    Emmert, D.E.2
  • 25
    • 0242696937 scopus 로고
    • Thermal rearrangements of 3-(hydroxyphenyl)-3-methyl-3H-indole
    • Robinson B, Uppal Zubair M: Thermal rearrangements of 3-(hydroxyphenyl)-3-methyl-3H-indole. Pakistan J Sci Ind Res (1976) 19(5-6):214-214.
    • (1976) Pakistan J Sci Ind Res , vol.19 , Issue.5-6 , pp. 214-214
    • Robinson, B.1    Uppal Zubair, M.2
  • 26
    • 0037419156 scopus 로고    scopus 로고
    • Study of the addition of Grignard reagents to 2-aryl-3H-indole-3-ones
    • Liu Y, McWhorter WW Jr: Study of the addition of Grignard reagents to 2-aryl-3H-indole-3-ones. J Org Chem (2003) 68(7):2618-2622. A systematic investigation of the rearrangement of 3H-indol-3-ols to indolin-3-ones.
    • (2003) J Org Chem , vol.68 , Issue.7 , pp. 2618-2622
    • Liu, Y.1    McWhorter Jr., W.W.2
  • 27
    • 37049111877 scopus 로고
    • Competition between single electron transfer and nucleophilic attack. Part 2. Reaction of 2-phenyl-3H-indol-3-one with Grignard reagents
    • Berti C, Greci L, Marchetti L: Competition between single electron transfer and nucleophilic attack. Part 2. Reaction of 2-phenyl-3H-indol-3-one with Grignard reagents. J Chem Soc Perkin Trans 2 (1979) (3):233-236.
    • (1979) J Chem Soc Perkin Trans 2 , Issue.3 , pp. 233-236
    • Berti, C.1    Greci, L.2    Marchetti, L.3
  • 28
    • 0013312654 scopus 로고
    • Nucleophilic reactions of 2-phenylindolenin-3-ones
    • Adam JM, Winkler T: Nucleophilic reactions of 2-phenylindolenin-3-ones. Helv Chim Acta (1984) 67(8):2186-2191.
    • (1984) Helv Chim Acta , vol.67 , Issue.8 , pp. 2186-2191
    • Adam, J.M.1    Winkler, T.2
  • 29
    • 0038518310 scopus 로고    scopus 로고
    • Novel rearrangement of a 2-aryl-3-alkyl-3H-indol-3-ol to a 1,4,5,6-tetrahydro-2,6-methano-1-benzazocin-3(2H)-one with implications for the biosynthesis of aspernomine
    • Liu Y, McWhorter WW Jr, Hadden CE: Novel rearrangement of a 2-aryl-3-alkyl-3H-indol-3-ol to a 1,4,5,6-tetrahydro-2,6-methano-1-benzazocin-3(2H)-one with implications for the biosynthesis of aspernomine. Org Lett (2003) 5(3):333-335. A new rearrangement of 3-alkenyl-3H-indol-3-ols.
    • (2003) Org Lett , vol.5 , Issue.3 , pp. 333-335
    • Liu, Y.1    McWhorter Jr., W.W.2    Hadden, C.E.3
  • 30
    • 0002900717 scopus 로고
    • Nominine: A new insecticidal indole diterpene from the sclerotia of Aspergillus nomius
    • Gloer JB, Rinderknecht BL, Wicklow DT, Dowd PF: Nominine: A new insecticidal indole diterpene from the sclerotia of Aspergillus nomius. J Org Chem (1989) 54(11):2530-2532.
    • (1989) J Org Chem , vol.54 , Issue.11 , pp. 2530-2532
    • Gloer, J.B.1    Rinderknecht, B.L.2    Wicklow, D.T.3    Dowd, P.F.4
  • 31
    • 0026501135 scopus 로고
    • Aspernomine: A cytotoxic antiinsectan metabolite with a novel ring system from the sclerotia of Aspergillus nomius
    • Staub GM, Gloer JB, Wicklow DT, Dowd PF: Aspernomine: A cytotoxic antiinsectan metabolite with a novel ring system from the sclerotia of Aspergillus nomius. J Am Chem Soc (1992) 114(3):1015-1017.
    • (1992) J Am Chem Soc , vol.114 , Issue.3 , pp. 1015-1017
    • Staub, G.M.1    Gloer, J.B.2    Wicklow, D.T.3    Dowd, P.F.4
  • 32
    • 33947481191 scopus 로고
    • Aminoketone rearrangement. II. The rearrangement of phenyl α-aminoketones
    • Stevens CL, Elliott RD, Winch BL: Aminoketone rearrangement. II. The rearrangement of phenyl α-aminoketones J Am Chem Soc (1963) 85(10):1464-1470. The first reported rearrangement of α-hydroxy imines to α-amino ketones in an acyclic system.
    • (1963) J Am Chem Soc , vol.85 , Issue.10 , pp. 1464-1470
    • Stevens, C.L.1    Elliott, R.D.2    Winch, B.L.3
  • 34
    • 0025253132 scopus 로고
    • Thermal rearrangement of α-hydroxy imines with an α-allyl or an α-propargyl substituent
    • Vatèle JM, Dumas D, Goré J: Thermal rearrangement of α-hydroxy imines with an α-allyl or an α-propargyl substituent. Tetrahedron Lett (1990) 31 (16):2277-2280.
    • (1990) Tetrahedron Lett , vol.31 , Issue.16 , pp. 2277-2280
    • Vatèle, J.M.1    Dumas, D.2    Goré, J.3
  • 35
    • 0029033547 scopus 로고
    • Thermal rearrangement of enantioenriched α-hydroxy imines - I. Enantiocontrolled synthesis of α-substituted α-amino ketones
    • Compain P, Goré J, Vatèle JM: Thermal rearrangement of enantioenriched α-hydroxy imines - I. Enantiocontrolled synthesis of α-substituted α-amino ketones. Tetrahedron Lett (1995) 36(23):4059-4062. The observation of chirality transfer in the rearrangement of α-hydroxy imines to α-amino ketones.
    • (1995) Tetrahedron Lett , vol.36 , Issue.23 , pp. 4059-4062
    • Compain, P.1    Goré, J.2    Vatèle, J.M.3
  • 36
    • 0029932015 scopus 로고    scopus 로고
    • Rearrangement of α-hydroxy imines to α-amino ketones: Mechanistic aspects and synthetic applications
    • Compain P, Goré J, Vatèle JM: Rearrangement of α-hydroxy imines to α-amino ketones: Mechanistic aspects and synthetic applications. Tetrahedron (1996) 52(19):6647-6664.
    • (1996) Tetrahedron , vol.52 , Issue.19 , pp. 6647-6664
    • Compain, P.1    Goré, J.2    Vatèle, J.M.3
  • 37
    • 0029867934 scopus 로고    scopus 로고
    • Synthesis and reactivity of (3-oxo-2,3-dihydro-1H-ylidene)acetic acid alkyl esters in Diels-Alder reaction
    • Mérour JY, Chichereau L, Desarbre E, Gadonneix P: Synthesis and reactivity of (3-oxo-2,3-dihydro-1H-ylidene)acetic acid alkyl esters in Diels-Alder reaction. Synthesis (1996) (4):519-524.
    • (1996) Synthesis , Issue.4 , pp. 519-524
    • Mérour, J.Y.1    Chichereau, L.2    Desarbre, E.3    Gadonneix, P.4
  • 38
    • 0032542111 scopus 로고    scopus 로고
    • Synthesis of sterically hindered 4a,9a-disubstituted 1,2,3,4,4a,9a-hexahydrocarbazoles from 4a-methyl-1,2,3,4-tetrahydro-4aH-carbazole with organolithium reagents
    • Rodríguez JG, Urrutia A: Synthesis of sterically hindered 4a,9a-disubstituted 1,2,3,4,4a,9a-hexahydrocarbazoles from 4a-methyl-1,2,3,4-tetrahydro-4aH-carbazole with organolithium reagents. Tetrahedron (1998) 54(51):15613-15618.
    • (1998) Tetrahedron , vol.54 , Issue.51 , pp. 15613-15618
    • Rodríguez, J.G.1    Urrutia, A.2
  • 39
    • 0037427238 scopus 로고    scopus 로고
    • 1
    • 1. J Am Chem Soc (2003) 125(14):4240-4252. The successful synthesis of the hinckdentine A framework, and a study of its bromination.
    • (2003) J Am Chem Soc , vol.125 , Issue.14 , pp. 4240-4252
    • Liu, Y.1    McWhorter, W.W.2
  • 40
    • 0000831146 scopus 로고
    • The reaction of indolyl Grignard and related organometallic reagents with 2-phenylsulphonylbuta-1,3-diene and 2,3-diphenylsulphonylbuta-1,3-diene
    • Barnwell N, Beddoes RL, Mitchell MB, Joule JA: The reaction of indolyl Grignard and related organometallic reagents with 2-phenylsulphonylbuta-1,3-diene and 2,3-diphenylsulphonylbuta-1,3-diene. Heterocycles (1994) 37(1):175-179. An approach to the hinckdentine A framework.
    • (1994) Heterocycles , vol.37 , Issue.1 , pp. 175-179
    • Barnwell, N.1    Beddoes, R.L.2    Mitchell, M.B.3    Joule, J.A.4
  • 41
    • 0027943707 scopus 로고
    • Chemistry of indolo[1,2-c]quinazoline: An approach to the marine alkaloid hinckdentine A
    • Billimoria AD, Cava MP: Chemistry of indolo[1,2-c]quinazoline: An approach to the marine alkaloid hinckdentine A. J Org Chem (1994) 59(22):6777-6782. An approach to the hinckdentine A framework.
    • (1994) J Org Chem , vol.59 , Issue.22 , pp. 6777-6782
    • Billimoria, A.D.1    Cava, M.P.2
  • 42
    • 0001282972 scopus 로고
    • Facile cycloaddition of 2-phenylsulfonyl 1,3-dienes to indoles
    • Bäckvall JE, Plobeck NA, Juntunen SK: Facile cycloaddition of 2-phenylsulfonyl 1,3-dienes to indoles. Tetrahedron Lett (1989) 30(19):2589-2592.
    • (1989) Tetrahedron Lett , vol.30 , Issue.19 , pp. 2589-2592
    • Bäckvall, J.E.1    Plobeck, N.A.2    Juntunen, S.K.3
  • 44
    • 37049116055 scopus 로고
    • A synthesis of (-)-(R)-trans-β -(1,2,3-trimethylcyclopent-2-enyl)acrylic acid
    • Fleming I, Woodward RB: A synthesis of (-)-(R)-trans-β -(1,2,3-trimethylcyclopent-2-enyl)acrylic acid. J Chem Soc Perkin Trans 1 (1973) (16):1653-1657.
    • (1973) J Chem Soc Perkin Trans 1 , Issue.16 , pp. 1653-1657
    • Fleming, I.1    Woodward, R.B.2
  • 45
    • 0032039627 scopus 로고    scopus 로고
    • Vanadium bromoperoxidases
    • Butler A: Vanadium bromoperoxidases. Curr Opin Chem Biol (1998) 2(2):279-285. Vanadium bromoperoxidase is believed to be responsible for the biosynthetic introduction of bromine into many marine natural products.
    • (1998) Curr Opin Chem Biol , vol.2 , Issue.2 , pp. 279-285
    • Butler, A.1
  • 46
    • 85081426152 scopus 로고    scopus 로고
    • 6-Substituted-indolo[1,2-c]-quinazolines. US-03635966 (1972)
    • AH ROBINS COMPANY INC (Duncan RL): 6-Substituted-indolo[1,2-c]-quinazolines. US-03635966 (1972).
    • Duncan, R.L.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.