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Volumn 37, Issue 9, 2007, Pages 1579-1585

I-/IO3- assemblies as promoters of iodohydrin formation

Author keywords

Iodohydrins; Olefins; Potassium iodate; Potassium iodide

Indexed keywords

ALKENE DERIVATIVE; IODINE DERIVATIVE; IODOHYDRIN; METAL; UNCLASSIFIED DRUG;

EID: 34248585885     PISSN: 00397911     EISSN: 15322432     Source Type: Journal    
DOI: 10.1080/00397910701239031     Document Type: Article
Times cited : (7)

References (27)
  • 2
    • 34248510616 scopus 로고
    • 4th ed, John Wiley & Sons: New York
    • (b) March, J. Advanced Organic Chemistry 4th ed.; John Wiley & Sons: New York, 1992, pp. 814-815;
    • (1992) J. Advanced Organic Chemistry , pp. 814-815
    • March1
  • 4
    • 37049140827 scopus 로고
    • Iodohydrins and epoxides from olefins
    • (a) Cornforth, J. W.; Green, D. T. Iodohydrins and epoxides from olefins. J. Chem. Soc. C 1970, 846-849;
    • (1970) J. Chem. Soc. C , pp. 846-849
    • Cornforth, J.W.1    Green, D.T.2
  • 5
    • 0005823223 scopus 로고
    • Bromohydrins from olefins and N-bromosuccinimide in water
    • (b) Guss, C. O.; Rosanthal, R. Bromohydrins from olefins and N-bromosuccinimide in water. J. Am. Chem. Soc. 1955, 77, 2549;
    • (1955) J. Am. Chem. Soc , vol.77 , pp. 2549
    • Guss, C.O.1    Rosanthal, R.2
  • 6
    • 33947465889 scopus 로고
    • The acid-catalyzed rearrangement of the stilbene oxides
    • (c) House, H. O. The acid-catalyzed rearrangement of the stilbene oxides. J. Am. Chem. Soc. 1955, 77, 3070-3075;
    • (1955) J. Am. Chem. Soc , vol.77 , pp. 3070-3075
    • House, H.O.1
  • 7
    • 0001071070 scopus 로고
    • Bromohydrin formation in dimethyl sulfoxide
    • (d) Dalton, D. R.; Dutta, V. P.; Jones, D. G. Bromohydrin formation in dimethyl sulfoxide. J. Am. Chem. Soc. 1968, 90, 5498-5501;
    • (1968) J. Am. Chem. Soc , vol.90 , pp. 5498-5501
    • Dalton, D.R.1    Dutta, V.P.2    Jones, D.G.3
  • 8
    • 0000651831 scopus 로고    scopus 로고
    • Sisti, A. J. Ring enlargement procedure, IV: Decomposition of the magnesium salts of various 1-(1-bromethyl)-1-cycloalkanols. J. Org. Chem. 1970, 35, 2670-2673;
    • (e) Sisti, A. J. Ring enlargement procedure, IV: Decomposition of the magnesium salts of various 1-(1-bromethyl)-1-cycloalkanols. J. Org. Chem. 1970, 35, 2670-2673;
  • 9
    • 0002961285 scopus 로고
    • Bromohydrin formation in aqueous dimethylsulphoxide: Electronic and steric effects
    • (f) Dalton, D. R.; Dutta, V. P. Bromohydrin formation in aqueous dimethylsulphoxide: Electronic and steric effects. J. Chem. Soc. B 1971, 85-89;
    • (1971) J. Chem. Soc. B , pp. 85-89
    • Dalton, D.R.1    Dutta, V.P.2
  • 10
    • 33845375078 scopus 로고
    • Synthesis of dihydro diols and diol epoxides of benzo[f]quinoline
    • (h) Dubey, S. K.; Kumar, S. Synthesis of dihydro diols and diol epoxides of benzo[f]quinoline. J. Org. Chem. 1986, 51, 3407-3412;
    • (1986) J. Org. Chem , vol.51 , pp. 3407-3412
    • Dubey, S.K.1    Kumar, S.2
  • 11
    • 0023241856 scopus 로고
    • Functionalized pyrazoles from indazol-4-ols
    • (g) LeTourneau, M. E.; Peet, N. P. Functionalized pyrazoles from indazol-4-ols. J. Org. Chem. 1987, 52, 4384-4387.
    • (1987) J. Org. Chem , vol.52 , pp. 4384-4387
    • LeTourneau, M.E.1    Peet, N.P.2
  • 12
    • 33947470048 scopus 로고
    • Mechanisms of epoxide reactions
    • (a) Parker, R. E.; Isaacs, N. S. Mechanisms of epoxide reactions. Chem. Rev. 1959, 59, 737-799;
    • (1959) Chem. Rev , vol.59 , pp. 737-799
    • Parker, R.E.1    Isaacs, N.S.2
  • 13
    • 0028196798 scopus 로고
    • Regio- and chemoselective synthesis of halohydrins by cleavage of oxiranes with metal halides
    • (b) Bonini, C.; Righi, G. Regio- and chemoselective synthesis of halohydrins by cleavage of oxiranes with metal halides. Synthesis 1994, 225-238;
    • (1994) Synthesis , pp. 225-238
    • Bonini, C.1    Righi, G.2
  • 14
    • 0037157814 scopus 로고    scopus 로고
    • Highly facile biomimetic regioselective ring opening of epoxides to halohydrins in the presence of β-cyclodextrin
    • (c) Reddy, M. A.; Surendra, K.; Bhanumathi, N.; Ramarao, K. Highly facile biomimetic regioselective ring opening of epoxides to halohydrins in the presence of β-cyclodextrin. Tetrahedron 2002, 58, 6003-6008;
    • (2002) Tetrahedron , vol.58 , pp. 6003-6008
    • Reddy, M.A.1    Surendra, K.2    Bhanumathi, N.3    Ramarao, K.4
  • 15
    • 0035833088 scopus 로고    scopus 로고
    • The halogen-mediated opening of epoxides in the presence of pyridine-containing macrocycles
    • (d) Sharghi, H.; Niknam, K.; Pooyan, M. The halogen-mediated opening of epoxides in the presence of pyridine-containing macrocycles. Tetrahedron 2001, 57, 6057-6064;
    • (2001) Tetrahedron , vol.57 , pp. 6057-6064
    • Sharghi, H.1    Niknam, K.2    Pooyan, M.3
  • 17
    • 1242339416 scopus 로고
    • A novel stability sequence of lanthanoid complexes with 1,2-bis(o-aminophenoxy)ethane-N,N,N,N-tetraacetic acid
    • (a) Ohta, H.; Sakata, Y.; Takeuchi, T.; Ishii, Y. A novel stability sequence of lanthanoid complexes with 1,2-bis(o-aminophenoxy)ethane-N,N,N,N-tetraacetic acid. Chem. Lett. 1990, 773-736;
    • (1990) Chem. Lett , pp. 773-736
    • Ohta, H.1    Sakata, Y.2    Takeuchi, T.3    Ishii, Y.4
  • 19
  • 20
    • 17844385054 scopus 로고    scopus 로고
    • Green approach for the conversion of olefins into vic-halohydrins using N-halosuccinimide in ionic liquids
    • Yadav, J. S.; Reddy, B. V. S.; Baishya, G.; Harshavardhan, S. J.; Chary, C. J.; Guptha, M. K. Green approach for the conversion of olefins into vic-halohydrins using N-halosuccinimide in ionic liquids. Tetrahedron Lett. 2005, 46, 3569-3572.
    • (2005) Tetrahedron Lett , vol.46 , pp. 3569-3572
    • Yadav, J.S.1    Reddy, B.V.S.2    Baishya, G.3    Harshavardhan, S.J.4    Chary, C.J.5    Guptha, M.K.6
  • 22
  • 24
    • 19644382379 scopus 로고    scopus 로고
    • Ionic liquid as reagent: A green procedure for the regioselective conversion of epoxides to vicinal-halohydrins using [AcMIm]X under catalyst and solvent-free conditions
    • Ranu, B. C.; Banerjee, S. Ionic liquid as reagent: A green procedure for the regioselective conversion of epoxides to vicinal-halohydrins using [AcMIm]X under catalyst and solvent-free conditions. J. Org. Chem. 2005, 70, 4517-4519.
    • (2005) J. Org. Chem , vol.70 , pp. 4517-4519
    • Ranu, B.C.1    Banerjee, S.2
  • 25
    • 57249095480 scopus 로고    scopus 로고
    • EPZ-10 catalyzed regioselective transformation of alkenes into β-iodo ethers, iodohydrins and 2-iodomethyl-2,3-dihydrobenzofurans
    • Mahajan, V. A.; Shinde, P. D.; Gajare, A. S.; Karthikeyan, M.; Wakharkar, R. D. EPZ-10 catalyzed regioselective transformation of alkenes into β-iodo ethers, iodohydrins and 2-iodomethyl-2,3-dihydrobenzofurans. Green Chem. 2002, 4, 325-327.
    • (2002) Green Chem , vol.4 , pp. 325-327
    • Mahajan, V.A.1    Shinde, P.D.2    Gajare, A.S.3    Karthikeyan, M.4    Wakharkar, R.D.5
  • 26
    • 0038180377 scopus 로고    scopus 로고
    • A new, environment friendly protocol for iodination of electron-rich aromatic compounds
    • (a) Adimurthy, S.; Ramachandraiah, G.; Ghosh, P. K.; Bedekar, A. V. A new, environment friendly protocol for iodination of electron-rich aromatic compounds. Tetrahedron Lett. 2003, 44, 5099-5100;
    • (2003) Tetrahedron Lett , vol.44 , pp. 5099-5100
    • Adimurthy, S.1    Ramachandraiah, G.2    Ghosh, P.K.3    Bedekar, A.V.4
  • 27
    • 33749508729 scopus 로고    scopus 로고
    • Ecofriendly and versatile brominating reagent prepared from liquid bromine precursor
    • 10.1039/b606586d
    • (b) Adimurthy, S.; Ramachandraiah, G.; Bedekar, A. V.; Ghosh, S.; Ranu, B. C.; Ghosh, P. K. Ecofriendly and versatile brominating reagent prepared from liquid bromine precursor. Green Chem. 2006, 8, 916-922; 10.1039/b606586d.
    • (2006) Green Chem , vol.8 , pp. 916-922
    • Adimurthy, S.1    Ramachandraiah, G.2    Bedekar, A.V.3    Ghosh, S.4    Ranu, B.C.5    Ghosh, P.K.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.