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Volumn 37, Issue 5, 2007, Pages 783-793

Convenient preparation of benzylseleno- and phenylselenoalkanoic acids: Reagents for synthesis of organoselenium compounds

Author keywords

Benzylselenoalkanoic acid; Ethyl benzylselenoalkanoates; Ethyl phenylselenoalkanoates; Phenylselenoalkanoic acid

Indexed keywords

ALKANE DERIVATIVE; ALKANOIC ACID; BENZYL DERIVATIVE; ORGANOSELENIUM DERIVATIVE; SELENIUM DERIVATIVE; SODIUM BOROHYDRIDE;

EID: 33847132743     PISSN: 00397911     EISSN: 15322432     Source Type: Journal    
DOI: 10.1080/00397910601133540     Document Type: Article
Times cited : (25)

References (22)
  • 1
    • 26844478247 scopus 로고
    • Selenium: Physiological and pharmacological roles of selenocompounds
    • Tanaka, J. Selenium: Physiological and pharmacological roles of selenocompounds. Kikan Kagaku Sosetsu 1995, 27, 120-131;
    • (1995) Kikan Kagaku Sosetsu , vol.27 , pp. 120-131
    • Tanaka, J.1
  • 2
    • 33847151162 scopus 로고    scopus 로고
    • Chem. Abstr. 1996, 124, 338600 .
    • Chem. Abstr. 1996, 124, 338600 .
  • 4
    • 1842388071 scopus 로고
    • Selenium as an integral part of factor 3 against dietary necrotic liver degeneration
    • Schwarz, K.; Foltz, C. M. Selenium as an integral part of factor 3 against dietary necrotic liver degeneration. J. Am. Chem. Soc. 1957, 79, 3292-3293.
    • (1957) J. Am. Chem. Soc , vol.79 , pp. 3292-3293
    • Schwarz, K.1    Foltz, C.M.2
  • 5
    • 0003629457 scopus 로고
    • Gunther, W. H, Ed, Wiley-Interscience: New York
    • Klayman, D. L. Organic Selenium Compounds; Gunther, W. H., Ed.; Wiley-Interscience: New York, 1973.
    • (1973) Organic Selenium Compounds
    • Klayman, D.L.1
  • 6
    • 49349139760 scopus 로고
    • Modern organoselenium chemistry
    • Clive, D. L. J. Modern organoselenium chemistry. Tetrahedron 1978, 34, 1049-1132.
    • (1978) Tetrahedron , vol.34 , pp. 1049-1132
    • Clive, D.L.J.1
  • 7
    • 0034625381 scopus 로고    scopus 로고
    • Preparation of 5-selenopentopyranose sugars from pentose starting materials by samarium (II) iodide or (phenylseleno) formate mediated ring closures
    • Lucas, M. A.; Nguyen, O. T. K.; Schiesser, C. H.; Zhend, S. L. Preparation of 5-selenopentopyranose sugars from pentose starting materials by samarium (II) iodide or (phenylseleno) formate mediated ring closures. Tetrahedron 2000, 56, 3995-4000.
    • (2000) Tetrahedron , vol.56 , pp. 3995-4000
    • Lucas, M.A.1    Nguyen, O.T.K.2    Schiesser, C.H.3    Zhend, S.L.4
  • 8
    • 0035929424 scopus 로고    scopus 로고
    • Intramolecular homolytic substitution at selenium: Synthesis of novel selenium-containing vitamin E analogues
    • Al-Maharik, N.; Engman, L.; Malmström, J.; Schiesser, C. H. Intramolecular homolytic substitution at selenium: Synthesis of novel selenium-containing vitamin E analogues. J. Org. Chem. 2001, 66, 6286-6290.
    • (2001) J. Org. Chem , vol.66 , pp. 6286-6290
    • Al-Maharik, N.1    Engman, L.2    Malmström, J.3    Schiesser, C.H.4
  • 10
    • 0025677291 scopus 로고
    • Spiro indolinone beta-lactams, inhibitors of poliovirus and rhinovirus 3C- proteinases
    • Skiles, J. W.; McNeil, D. Spiro indolinone beta-lactams, inhibitors of poliovirus and rhinovirus 3C- proteinases. Tetrahedron Lett. 1990, 31, 7277-7280.
    • (1990) Tetrahedron Lett , vol.31 , pp. 7277-7280
    • Skiles, J.W.1    McNeil, D.2
  • 11
    • 0036262532 scopus 로고    scopus 로고
    • A novel β-lactam antibiotic activates tumor cell apoptotic program by inducing DNA damage
    • Smith, D. M.; Kazi, A.; Smith, L.; Long, T. E.; Heldreth, B.; Turos, E.; Dou, Q. P. A novel β-lactam antibiotic activates tumor cell apoptotic program by inducing DNA damage. Mol. Pharmacol. 2002, 61, 1348-1358.
    • (2002) Mol. Pharmacol , vol.61 , pp. 1348-1358
    • Smith, D.M.1    Kazi, A.2    Smith, L.3    Long, T.E.4    Heldreth, B.5    Turos, E.6    Dou, Q.P.7
  • 12
    • 0034662131 scopus 로고    scopus 로고
    • A new synthetic approach for novel C-3 substituted β-lactams
    • Madan, S.; Arora, R.; Venugopalan, P.; Bari, S. S. A new synthetic approach for novel C-3 substituted β-lactams. Tetrahedron Lett. 2000, 41, 5577-5581.
    • (2000) Tetrahedron Lett , vol.41 , pp. 5577-5581
    • Madan, S.1    Arora, R.2    Venugopalan, P.3    Bari, S.S.4
  • 13
    • 0037467885 scopus 로고    scopus 로고
    • A facile Lewis acid-promoted allylation of azetidin-2-ones
    • Bari, S. S.; Venugopalan, P.; Arora, R. A facile Lewis acid-promoted allylation of azetidin-2-ones. Tetrahedron Lett. 2003, 44, 895-897.
    • (2003) Tetrahedron Lett , vol.44 , pp. 895-897
    • Bari, S.S.1    Venugopalan, P.2    Arora, R.3
  • 14
    • 33745673839 scopus 로고    scopus 로고
    • An unusual Lewis acid promoted isomerization of trans-3-halophenylthio-β- lactams
    • Bari, S. S.; Venugopalan, P.; Arora, R.; Modi, G.; Madan, S. An unusual Lewis acid promoted isomerization of trans-3-halophenylthio-β- lactams. Heterocycles 2006, 68, 749-762.
    • (2006) Heterocycles , vol.68 , pp. 749-762
    • Bari, S.S.1    Venugopalan, P.2    Arora, R.3    Modi, G.4    Madan, S.5
  • 15
    • 33745967991 scopus 로고    scopus 로고
    • C-3 β-Lactam carbocation equivalents: Versatile synthons for C-3 substituted β-lactams
    • Bhalla, A.; Madan, S.; Venugopalan, P.; Bari, S. S. C-3 β-Lactam carbocation equivalents: Versatile synthons for C-3 substituted β-lactams. Tetrahedron 2006, 62, 5054-5063.
    • (2006) Tetrahedron , vol.62 , pp. 5054-5063
    • Bhalla, A.1    Madan, S.2    Venugopalan, P.3    Bari, S.S.4
  • 16
    • 33745190270 scopus 로고    scopus 로고
    • Lewis acid mediated functionalization of β-lactams: Mechanistic study and synthesis of C-3 unsymmetrically disubstituted azetidin-2-ones
    • Bhalla, A.; Rathee, S.; Madan, S.; Venugopalan, P.; Bari, S. S. Lewis acid mediated functionalization of β-lactams: Mechanistic study and synthesis of C-3 unsymmetrically disubstituted azetidin-2-ones. Tetrahedron Lett. 2006, 47, 5255-5259.
    • (2006) Tetrahedron Lett , vol.47 , pp. 5255-5259
    • Bhalla, A.1    Rathee, S.2    Madan, S.3    Venugopalan, P.4    Bari, S.S.5
  • 17
    • 33745958470 scopus 로고    scopus 로고
    • Facile stereoselective synthesis of cis- and trans-3-alkoxyazetidin-2-ones
    • Bhalla, A.; Venugopalan, P.; Bari, S. S. Facile stereoselective synthesis of cis- and trans-3-alkoxyazetidin-2-ones. Tetrahedron 2006, 62, 8291-8302.
    • (2006) Tetrahedron , vol.62 , pp. 8291-8302
    • Bhalla, A.1    Venugopalan, P.2    Bari, S.S.3
  • 18
    • 3242886230 scopus 로고    scopus 로고
    • Preparation of novel selenopenams by intramolecular homolytic substitution
    • Carland, M. W.; Schiesser, C. H. Preparation of novel selenopenams by intramolecular homolytic substitution. Molecules 2004, 9, 466-471.
    • (2004) Molecules , vol.9 , pp. 466-471
    • Carland, M.W.1    Schiesser, C.H.2
  • 19
    • 33847163928 scopus 로고
    • Some benzylseleno- and β-phenylethylseleno-substituted alkanoic acids
    • Fredga, A. Some benzylseleno- and β-phenylethylseleno-substituted alkanoic acids. Acta Chem. Scand. B 1974, 28, 692-694.
    • (1974) Acta Chem. Scand. B , vol.28 , pp. 692-694
    • Fredga, A.1
  • 20
    • 0027522635 scopus 로고
    • Homolytic substitution at selenium: Ring closure of ω-(benzylseleno)alkyl radicals
    • Benjamin, L. J.; Schiesser, C. H.; Sutej, K. Homolytic substitution at selenium: ring closure of ω-(benzylseleno)alkyl radicals. Tetrahedron 1993, 49, 2557-2566.
    • (1993) Tetrahedron , vol.49 , pp. 2557-2566
    • Benjamin, L.J.1    Schiesser, C.H.2    Sutej, K.3
  • 22
    • 0007590568 scopus 로고
    • A mild procedure for the conversion of epoxides to allylic alcohols: The first organoselenium reagent
    • Sharpless, K. B.; Lauer, R. F. J. A mild procedure for the conversion of epoxides to allylic alcohols: The first organoselenium reagent. J. Am. Chem. Soc. 1973, 95, 2697-2699.
    • (1973) J. Am. Chem. Soc , vol.95 , pp. 2697-2699
    • Sharpless, K.B.1    Lauer, R.F.J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.