메뉴 건너뛰기




Volumn 34, Issue 23, 2004, Pages 4409-4415

VO(acac)2 catalyzed oxidative deprotection of oximes, hydrazones, and semicarbazones

Author keywords

Hydrazones; Oximes; Semicarbazones; Vanadyl acetyl acetonate

Indexed keywords

ACETONE; ACETYLACETONATE VANADIUM; HYDRAZONE DERIVATIVE; HYDROGEN PEROXIDE; OXIME; SEMICARBAZONE DERIVATIVE; UNCLASSIFIED DRUG; VANADYL DERIVATIVE;

EID: 10644264335     PISSN: 00397911     EISSN: None     Source Type: Journal    
DOI: 10.1081/SCC-200039490     Document Type: Article
Times cited : (10)

References (24)
  • 3
    • 33947442275 scopus 로고
    • Regeneration of steroid ketones from their semicarbazones with pyruvic acid
    • Hersberg, E.B. Regeneration of Steroid Ketones from Their Semicarbazones with Pyruvic Acid. J. Org. Chem. 1948, 13, 542-546.
    • (1948) J. Org. Chem. , vol.13 , pp. 542-546
    • Hersberg, E.B.1
  • 5
    • 26844554597 scopus 로고    scopus 로고
    • A mild versatile method for the oxidative cleavage of oximes and tosylhydrazones to carbonyl compounds
    • Bose, S.D.; Srinivas, P. A Mild and Versatile Method for the Oxidative Cleavage of Oximes And Tosylhydrazones to Carbonyl Compounds. Synlett. 1998, 977-978.
    • (1998) Synlett , pp. 977-978
    • Bose, S.D.1    Srinivas, P.2
  • 7
    • 85038554964 scopus 로고
    • Rapid deoximation with pyridinium cholorochromate/hydrogen peroxide system
    • Drabowicz, J. Rapid Deoximation with Pyridinium Cholorochromate/Hydrogen Peroxide System. Synthesis 1980, 125-126.
    • (1980) Synthesis , pp. 125-126
    • Drabowicz, J.1
  • 8
    • 0000614649 scopus 로고
    • An efficient and highly selective method of deoximation of ketoxime
    • Chidambaram, N.; Satyanarayan, K.; Chandrasekhar, S. An Efficient and Highly Selective Method of Deoximation of Ketoxime. Synth. Commun. 1989, 19, 1727-1734.
    • (1989) Synth. Commun. , vol.19 , pp. 1727-1734
    • Chidambaram, N.1    Satyanarayan, K.2    Chandrasekhar, S.3
  • 9
    • 0031021674 scopus 로고    scopus 로고
    • Facile regeneration of carbonyl compounds from oximes and tosylhydrazones with TBHP
    • Barahate, N.B.; Gajare, A.S.; Waharkar, R.D.; Sudalai, A. Facile Regeneration of Carbonyl Compounds from Oximes and Tosylhydrazones with TBHP. Tetrahedron Lett. 1997, 38, 653-656.
    • (1997) Tetrahedron Lett. , vol.38 , pp. 653-656
    • Barahate, N.B.1    Gajare, A.S.2    Waharkar, R.D.3    Sudalai, A.4
  • 10
    • 0030695426 scopus 로고    scopus 로고
    • Manganese triacetate mediated regeneration of carbonyl compounds from oximes
    • Demir, A.S.; Tanyeli, C.; Altinel, E. Manganese Triacetate Mediated Regeneration of Carbonyl Compounds from Oximes. Tetrahedron Lett. 1997, 38, 7267-7270.
    • (1997) Tetrahedron Lett. , vol.38 , pp. 7267-7270
    • Demir, A.S.1    Tanyeli, C.2    Altinel, E.3
  • 11
    • 0037090104 scopus 로고    scopus 로고
    • Facile regeneration of carbonyl compounds from oximes using poly[4-vinyl-N,N-dichlobenzenesulfonamide]
    • Khazaei, A.; Vaghei, R.G. Facile Regeneration of Carbonyl Compounds from Oximes Using poly[4-vinyl-N,N-dichlobenzenesulfonamide]. Tetrahedron Lett. 2002, 43, 3073-3074.
    • (2002) Tetrahedron Lett. , vol.43 , pp. 3073-3074
    • Khazaei, A.1    Vaghei, R.G.2
  • 12
    • 0345276524 scopus 로고    scopus 로고
    • Bismuth compounds in organic synthesis deprotection of ketoximes using Bismuth bromide-Bismuth trifalte
    • Arnold, J.N.; Hayes, P.D.; Kohaus, R.L.; Mohan, R.M. Bismuth Compounds in Organic Synthesis Deprotection of Ketoximes Using Bismuth Bromide-Bismuth Trifalte. Tetrahedron Lett. 2003, 44, 9173-9175.
    • (2003) Tetrahedron Lett. , vol.44 , pp. 9173-9175
    • Arnold, J.N.1    Hayes, P.D.2    Kohaus, R.L.3    Mohan, R.M.4
  • 13
    • 0000827089 scopus 로고    scopus 로고
    • Deprotection of ketoximes using bismuth(III) nitrate pentahydrate
    • Nattier, B.A.; Eash, K.J.; Mohan, R.M. Deprotection of Ketoximes Using Bismuth(III) Nitrate Pentahydrate. Synthesis 2001, 1010-1012.
    • (2001) Synthesis , pp. 1010-1012
    • Nattier, B.A.1    Eash, K.J.2    Mohan, R.M.3
  • 15
    • 33845279971 scopus 로고
    • A simple efficient, and highly selective method for the regeneration of carbonyl compounds from oximes and semicarbazones
    • Ranu, B.C.; Sarkar, D.C. A Simple, Efficient, and Highly Selective Method for the Regeneration of Carbonyl Compounds from Oximes and Semicarbazones. J. Org. Chem. 1988, 53, 878-879.
    • (1988) J. Org. Chem. , vol.53 , pp. 878-879
    • Ranu, B.C.1    Sarkar, D.C.2
  • 16
    • 0030783694 scopus 로고    scopus 로고
    • Solid state regeneration of ketones from oximes on wet silica supported sodium periodate using microwaves
    • Varma, R.S.; Dahiya, R.; Saini, R.K. Solid State Regeneration of Ketones from Oximes on Wet Silica Supported Sodium Periodate Using Microwaves. Tetrahedron Lett. 1997, 38, 8819-8820.
    • (1997) Tetrahedron Lett. , vol.38 , pp. 8819-8820
    • Varma, R.S.1    Dahiya, R.2    Saini, R.K.3
  • 17
    • 0030950742 scopus 로고    scopus 로고
    • Regeneration of carbonyl compounds from oximes under microwave irradiation
    • Boruah, A.; Baruah, B.; Prajapati, D.; Sandhu, J.S. Regeneration of Carbonyl Compounds from Oximes under Microwave Irradiation. Tetrahedron Lett. 1997, 38, 4267-4268.
    • (1997) Tetrahedron Lett. , vol.38 , pp. 4267-4268
    • Boruah, A.1    Baruah, B.2    Prajapati, D.3    Sandhu, J.S.4
  • 18
    • 0242541938 scopus 로고    scopus 로고
    • 4/wet silica gel as an efficient heterogeneous system for cleavage of C=N
    • 4/Wet Silica Gel as an Efficient Heterogeneous System for Cleavage of C=N. Tetrahedron Lett. 2003, 44, 9055-9056.
    • (2003) Tetrahedron Lett. , vol.44 , pp. 9055-9056
    • De, S.K.1
  • 19
    • 0346392199 scopus 로고    scopus 로고
    • Cobalt(II) chloride catalyzed chemoselective thioacetalization of aldehydes
    • (a) De, S.K. Cobalt(II) Chloride Catalyzed Chemoselective Thioacetalization of Aldehydes. Tetrahedron Lett. 2004, 45, 1035-1036;
    • (2004) Tetrahedron Lett. , vol.45 , pp. 1035-1036
    • De, S.K.1
  • 20
    • 1242315559 scopus 로고    scopus 로고
    • Ytrrium triflate as an efficient and useful catalyst for chemoselective protection of carbonyl compounds
    • (b) De, S.K. Ytrrium Triflate as an Efficient and Useful Catalyst for Chemoselective Protection of Carbonyl Compounds. Tetrahedron Lett. 2004, 45, 2339.
    • (2004) Tetrahedron Lett. , vol.45 , pp. 2339
    • De, S.K.1
  • 21
    • 0035953013 scopus 로고    scopus 로고
    • Vanadyl acetylacetonate as peroxide activator in osmium-catalyzed dihydroxylation of olefins by hydrogen peroxide
    • (a) Ell, A.H.; Jonsson, S.Y.; Borje, A.; Adolfsson, H.; Backbvall, J.E. Vanadyl Acetylacetonate as Peroxide Activator in Osmium-Catalyzed Dihydroxylation of Olefins by Hydrogen Peroxide. Tetrahedron Lett. 2001, 42, 2569-2571;
    • (2001) Tetrahedron Lett. , vol.42 , pp. 2569-2571
    • Ell, A.H.1    Jonsson, S.Y.2    Borje, A.3    Adolfsson, H.4    Backbvall, J.E.5
  • 22
    • 0037414509 scopus 로고    scopus 로고
    • 2/TBHP mediated oxidation of o-alkenyl phenols to o-hydroxybenzyl ketones
    • 2/TBHP Mediated Oxidation of o-Alkenyl Phenols to o-Hydroxybenzyl Ketones. J. Org. Chem. 2003, 68, 3691-3694.
    • (2003) J. Org. Chem. , vol.68 , pp. 3691-3694
    • Lattanzi, A.1    Senatore, A.2    Massa, A.3    Scettri, A.4
  • 24
    • 10644227102 scopus 로고    scopus 로고
    • note
    • Bp and mp are available from Aldrich Chemical Company.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.