메뉴 건너뛰기




Volumn 24, Issue 2, 2013, Pages 134-136

DABCO-promoted facile and convenient synthesis of novel isoxazolyl-1H-2,3-pyrrole dicarboxylates

Author keywords

DABCO; Isoxazolyl 1H 2,3 pyrroledicarboxylates; One pot three component reaction

Indexed keywords


EID: 84875247985     PISSN: 10018417     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cclet.2013.01.002     Document Type: Article
Times cited : (7)

References (26)
  • 1
    • 0001041971 scopus 로고
    • The Chemistry of Heterocyclic Compounds. Part 2: Pyrroles
    • R.A. Jones, Wiley New York
    • B.A. Trofimov The Chemistry of Heterocyclic Compounds. Part 2: Pyrroles R.A. Jones, Vinylpyrroles 1992 Wiley New York
    • (1992) Vinylpyrroles
    • Trofimov, B.A.1
  • 3
    • 0031836173 scopus 로고    scopus 로고
    • Cytotoxics derived from distamycin A and congeners
    • P. Cozzi, and N. Mongelli Cytotoxics derived from distamycin A and congeners Curr. Pharm. Des. 4 1998 181 194
    • (1998) Curr. Pharm. Des. , vol.4 , pp. 181-194
    • Cozzi, P.1    Mongelli, N.2
  • 4
    • 0032569211 scopus 로고    scopus 로고
    • Platinum- and acid-catalyzed enyne metathesis reactions mechanistic studies and applications to the syntheses of streptorubin B and metacyclo-prodigiosin
    • A. Furstner, H. Szillat, B. Gabor, and R.J. Mynott Platinum- and acid-catalyzed enyne metathesis reactions mechanistic studies and applications to the syntheses of streptorubin B and metacyclo-prodigiosin J. Am. Chem. Soc. 120 1998 8305 8314
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 8305-8314
    • Furstner, A.1    Szillat, H.2    Gabor, B.3    Mynott, R.J.4
  • 5
    • 0033550480 scopus 로고    scopus 로고
    • Total syntheses of ningalin A, lamellarin O, lukianol A and permethyl storniamide A utilizing heterocyclic azadiene Diels-Alder reactions
    • D.L. Boger, C.W. Boyce, M.A. Labroli, C.A. Sehon, and Q. Jin Total syntheses of ningalin A, lamellarin O, lukianol A and permethyl storniamide A utilizing heterocyclic azadiene Diels-Alder reactions J. Am. Chem. Soc. 121 1999 54 62
    • (1999) J. Am. Chem. Soc. , vol.121 , pp. 54-62
    • Boger, D.L.1    Boyce, C.W.2    Labroli, M.A.3    Sehon, C.A.4    Jin, Q.5
  • 6
    • 33750103589 scopus 로고    scopus 로고
    • An efficient and rapid synthesis of N-substitued pyrroles by microwave assisted solid acid catalysis
    • M. Abid, S.M. Landge, and B. Torok An efficient and rapid synthesis of N-substitued pyrroles by microwave assisted solid acid catalysis Org. Prep. Proced. Int. 38 2006 495 500
    • (2006) Org. Prep. Proced. Int. , vol.38 , pp. 495-500
    • Abid, M.1    Landge, S.M.2    Torok, B.3
  • 7
    • 0037432441 scopus 로고    scopus 로고
    • Layer-by-layer self-assembled pyrrole-based donor-acceptor chromophores as electro-optic materials
    • A. Facchetti, A. Abboto, and L. Beverina Layer-by-layer self-assembled pyrrole-based donor-acceptor chromophores as electro-optic materials Chem. Mater 15 2003 1064 1072
    • (2003) Chem. Mater , vol.15 , pp. 1064-1072
    • Facchetti, A.1    Abboto, A.2    Beverina, L.3
  • 8
    • 34250624466 scopus 로고    scopus 로고
    • Efficient synthesis and properties of isomeric photochromic diarylethenes having a pyrrole unit
    • S. Pu, J. Liu, L. Shen, and J. Xu Efficient synthesis and properties of isomeric photochromic diarylethenes having a pyrrole unit Org. Lett. 9 2007 2139 2142
    • (2007) Org. Lett. , vol.9 , pp. 2139-2142
    • Pu, S.1    Liu, J.2    Shen, L.3    Xu, J.4
  • 9
    • 1842674939 scopus 로고
    • Synthesis of 3-[-1,3-thiazol-2-yl]- as potential antitumor agents
    • J. Getal Synthesis of 3-[-1,3-thiazol-2-yl]- as potential antitumor agents Antibiotics 28 1975 91 93
    • (1975) Antibiotics , vol.28 , pp. 91-93
    • Getal, J.1
  • 10
    • 0342450306 scopus 로고
    • Isoxazoles. XVIII. Synthesis and pharmacological properties of 5-aminoalkyl- and 3-aminoalkylisoxazoles and related derivatives
    • H. Kano, I. Adachi, R. Kido, and K. Hirose Isoxazoles. XVIII. Synthesis and pharmacological properties of 5-aminoalkyl- and 3-aminoalkylisoxazoles and related derivatives J. Med. Chem. 10 1967 411 418
    • (1967) J. Med. Chem. , vol.10 , pp. 411-418
    • Kano, H.1    Adachi, I.2    Kido, R.3    Hirose, K.4
  • 11
  • 12
    • 84866115258 scopus 로고
    • Process for manufacturing alkylene carbonates using metal phthalocyanine catalysts, US Patent (1994) 5283356
    • E.T. Marquis, and J.R. Sanderson Process for manufacturing alkylene carbonates using metal phthalocyanine catalysts, US Patent (1994) 5283356 Chem. Abstr. 120 1994 217649
    • (1994) Chem. Abstr. , vol.120 , pp. 217649
    • Marquis, E.T.1    Sanderson, J.R.2
  • 13
    • 1842674938 scopus 로고
    • Production of chromosomal breaks by isoxazolyl thiazolidin-ome in allium sativu
    • A. Sadanadam, M.V. Rajam, K. Subash, and E. Rajanarendar Production of chromosomal breaks by isoxazolyl thiazolidin-ome in allium sativu Indian Bot. Rep. 3 1984 38 42
    • (1984) Indian Bot. Rep. , vol.3 , pp. 38-42
    • Sadanadam, A.1    Rajam, M.V.2    Subash, K.3    Rajanarendar, E.4
  • 15
    • 70349419649 scopus 로고    scopus 로고
    • The synthesis of polysubstituted pyrroles via the coupling of phenyl iodonium ylides and enamine esters
    • J.Y. Wang, X.P. Wang, Z.S. Yu, and W. Yu The synthesis of polysubstituted pyrroles via the coupling of phenyl iodonium ylides and enamine esters Adv. Synth. Catal. 351 2009 2063 2066
    • (2009) Adv. Synth. Catal. , vol.351 , pp. 2063-2066
    • Wang, J.Y.1    Wang, X.P.2    Yu, Z.S.3    Yu, W.4
  • 16
    • 77956564684 scopus 로고    scopus 로고
    • One-pot AgOAc-mediated synthesis of polysubstituted pyrroles from primary amines and aldehydes: Application to the total synthesis of purpurone
    • Q. Li, A. Fan, and Z. Lu One-pot AgOAc-mediated synthesis of polysubstituted pyrroles from primary amines and aldehydes: application to the total synthesis of purpurone Org. Lett. 12 2010 4066 4069
    • (2010) Org. Lett. , vol.12 , pp. 4066-4069
    • Li, Q.1    Fan, A.2    Lu, Z.3
  • 17
    • 77956537793 scopus 로고    scopus 로고
    • Synthesis of highly substituted pyrroles via nucleophilic catalyis
    • S. Ngwerume, and J. Camp Synthesis of highly substituted pyrroles via nucleophilic catalyis J. Org. Chem. 75 2010 6271 6274
    • (2010) J. Org. Chem. , vol.75 , pp. 6271-6274
    • Ngwerume, S.1    Camp, J.2
  • 18
    • 78651406983 scopus 로고    scopus 로고
    • Iron-catalyzed synthesis of poly substituted pyrroles via [4C+1N] cyclization of 4-acetylenic ketones with primary amines
    • Y. Wang, X. Bi, and D. Li Iron-catalyzed synthesis of poly substituted pyrroles via [4C+1N] cyclization of 4-acetylenic ketones with primary amines Chem. Commun. 47 2011 809 811
    • (2011) Chem. Commun. , vol.47 , pp. 809-811
    • Wang, Y.1    Bi, X.2    Li, D.3
  • 19
  • 20
    • 79952737475 scopus 로고    scopus 로고
    • Multi-component synthesis of methylene bis isoxazolo[4,5]-pyridine-N- oxide
    • E. Rajanarendar, M. Nagi Reddy, and K. Ramamurthy Multi-component synthesis of methylene bis isoxazolo[4,5]-pyridine-N-oxide Chin. Chem. Lett. 21 2010 927 930
    • (2010) Chin. Chem. Lett. , vol.21 , pp. 927-930
    • Rajanarendar, E.1    Nagi Reddy, M.2    Ramamurthy, K.3
  • 21
    • 77956900492 scopus 로고    scopus 로고
    • Synthesis, antimicrobial, and mosquito larvicidal activity of 1-aryl-4-methyly-3,6-bis-(5-methylisoxazol-3-yl)-2-thioxo-2,3,6, 10b-tetrahydro-1H-pyrimido[5,4-c]quinolin-5-ones
    • E. Rajanarendar, M. Nagi Reddy, and K. Ramamurthy Synthesis, antimicrobial, and mosquito larvicidal activity of 1-aryl-4-methyly-3,6-bis-(5- methylisoxazol-3-yl)-2-thioxo-2,3,6,10b-tetrahydro-1H-pyrimido[5,4-c] quinolin-5-ones Bioorg. Med. Chem. Lett. 20 2010 6052 6055
    • (2010) Bioorg. Med. Chem. Lett. , vol.20 , pp. 6052-6055
    • Rajanarendar, E.1    Nagi Reddy, M.2    Ramamurthy, K.3
  • 22
    • 84858445099 scopus 로고    scopus 로고
    • Multi component synthesis and in vitro and in vivo anticancer activity of novel arylmethylene bis-isoxazolo[4,5-b]pyridine-N-oxide
    • E. Rajanarendar, S. Raju, and M. Nagi Reddy Multi component synthesis and in vitro and in vivo anticancer activity of novel arylmethylene bis-isoxazolo[4,5-b]pyridine-N-oxide India Eur. J. Med. Chem. Lett. 50 2012 274 279
    • (2012) India Eur. J. Med. Chem. Lett. , vol.50 , pp. 274-279
    • Rajanarendar, E.1    Raju, S.2    Nagi Reddy, M.3
  • 23
    • 57449094374 scopus 로고    scopus 로고
    • Palladium-catalyzed Suzuki-Miyaura cross-coupling reaction of organoboronic acids with N-protected 4-iodophenyl alanine linked isoxazoles
    • E. Rajanarendar, G. Mohan, E. Kalyan Rao, and M. Srinivas Palladium-catalyzed Suzuki-Miyaura cross-coupling reaction of organoboronic acids with N-protected 4-iodophenyl alanine linked isoxazoles Chin. Chem. Lett. 10 2009 1 4
    • (2009) Chin. Chem. Lett. , vol.10 , pp. 1-4
    • Rajanarendar, E.1    Mohan, G.2    Kalyan Rao, E.3    Srinivas, M.4
  • 25
    • 0242552953 scopus 로고
    • The use of 3,5-dimethyl 4 nitro isoxazole for the preparation of α,β-unsaturated aromatic acids
    • A. Quilico, and C. Musante The use of 3,5-dimethyl 4 nitro isoxazole for the preparation of α,β-unsaturated aromatic acids Gazz. Chim. Ital. 72 1942 399
    • (1942) Gazz. Chim. Ital. , vol.72 , pp. 399
    • Quilico, A.1    Musante, C.2
  • 26
    • 0017056608 scopus 로고
    • Amides and Schiff bases from 4-aminoisoxazoles and their psysiological activity
    • A.K. Murthy, K.S.R.K.M. Rao, and N.V.S. Rao Amides and Schiff bases from 4-aminoisoxazoles and their psysiological activity J. Indian Chem. Soc. 53 1976 1047 1054
    • (1976) J. Indian Chem. Soc. , vol.53 , pp. 1047-1054
    • Murthy, A.K.1    Rao, K.S.R.K.M.2    Rao, N.V.S.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.