메뉴 건너뛰기




Volumn 35, Issue 10, 2005, Pages 1301-1305

Lithium chloride-assisted chemoselective conversion of aldehydes into geminal diacetates under solvent-free conditions

Author keywords

Acetic anhydride; Aldehydes; Diacetylation; Lithium chloride; Solvent free

Indexed keywords

ACETIC ANHYDRIDE; ACETOACETIC ACID; ALDEHYDE; LITHIUM CHLORIDE; SILICA GEL; SOLVENT;

EID: 19544374725     PISSN: 00397911     EISSN: None     Source Type: Journal    
DOI: 10.1081/SCC-200057238     Document Type: Article
Times cited : (4)

References (25)
  • 4
    • 0021407076 scopus 로고
    • Acetals as crosslinking reagents for cotton
    • (a) Frick, J. G., Jr.; Harper, R. J., Jr. Acetals as crosslinking reagents for cotton. J. Appl. Polym. Sci. 1984, 29, 1433-1447;
    • (1984) J. Appl. Polym. Sci. , vol.29 , pp. 1433-1447
    • Frick Jr., J.G.1    Harper Jr., R.J.2
  • 5
    • 19544372174 scopus 로고
    • Peroxygen compounds. Eur. Pat. Appl. EP125781
    • (b) Sanderson, W. R. Peroxygen compounds. Eur. Pat. Appl. 1985, EP125781, 57.
    • (1985) , pp. 57
    • Sanderson, W.R.1
  • 6
    • 0032572855 scopus 로고    scopus 로고
    • The chemistry of acylals: Part II. Formation of nitriles by treatment of acylals with trimethylsilyl azide in the presence of Lewis acid
    • (a) Sandberg, M.; Sydnes, L. K. The chemistry of acylals: Part II. Formation of nitriles by treatment of acylals with trimethylsilyl azide in the presence of Lewis acid. Tetrahedron Lett. 1998, 39, 6361-6364;
    • (1998) Tetrahedron Lett. , vol.39 , pp. 6361-6364
    • Sandberg, M.1    Sydnes, L.K.2
  • 8
    • 26844441037 scopus 로고    scopus 로고
    • 3, an efficient catalyst for formation and deprotectection of geminal diacetates (acylals); chemoselective protection of aldehydes in presence of ketones
    • 3, an efficient catalyst for formation and deprotectection of geminal diacetates (acylals); chemoselective protection of aldehydes in presence of ketones. Synlett 1998, 849-850.
    • (1998) Synlett , pp. 849-850
    • Aggarwal, V.K.1    Fonquerna, S.2    Vennal, G.P.3
  • 9
    • 0001721447 scopus 로고    scopus 로고
    • Iodine as acetylation catalyst in the preparation of 1,1-diacetates from aldehydes
    • Deka, N.; Kalita, D. J.; Borah, R.; Sarmah, J. C. Iodine as acetylation catalyst in the preparation of 1,1-diacetates from aldehydes. J. Org. Chem. 1997, 62, 1563-1564.
    • (1997) J. Org. Chem. , vol.62 , pp. 1563-1564
    • Deka, N.1    Kalita, D.J.2    Borah, R.3    Sarmah, J.C.4
  • 10
    • 0034032556 scopus 로고    scopus 로고
    • Mild and efficient conversion of aldehydes to 1,1-diacetates catalysed with N-bromosuccinimide (NBS)
    • Karimi, B.; Seradj, H.; Ebrahimian, G. R. Mild and efficient conversion of aldehydes to 1,1-diacetates catalysed with N-bromosuccinimide (NBS). Synlett 2000, 623-624.
    • (2000) Synlett , pp. 623-624
    • Karimi, B.1    Seradj, H.2    Ebrahimian, G.R.3
  • 13
    • 0037433809 scopus 로고    scopus 로고
    • 40) as an efficient heterogeneous inorganic catalyst for the chemoselective synthesis of geminal diacetates (acylals) under solvent-free conditions
    • 40) as an efficient heterogeneous inorganic catalyst for the chemoselective synthesis of geminal diacetates (acylals) under solvent-free conditions. Tetrahedron Lett. 2003, 44, 3951-3954.
    • (2003) Tetrahedron Lett. , vol.44 , pp. 3951-3954
    • Firouzabadi, H.1    Irapoor, N.2    Nowrouzi, F.3    Amani, K.4
  • 14
    • 0035851387 scopus 로고    scopus 로고
    • An efficient method for the chemoselective synthesis of acylals from aromatic aldehydes using bismuth triflate
    • Carrigan, M. D.; Eash, K. J.; Oswald, M. C.; Mohan, R. S. An efficient method for the chemoselective synthesis of acylals from aromatic aldehydes using bismuth triflate. Tetrahedron Lett. 2001, 42, 8133-8135.
    • (2001) Tetrahedron Lett. , vol.42 , pp. 8133-8135
    • Carrigan, M.D.1    Eash, K.J.2    Oswald, M.C.3    Mohan, R.S.4
  • 15
    • 0000884192 scopus 로고    scopus 로고
    • Solvent free organic synthesis
    • Tanaka, K.; Toda, F. Solvent free organic synthesis. Chem. Rev. 2000, 100, 1025-1074.
    • (2000) Chem. Rev. , vol.100 , pp. 1025-1074
    • Tanaka, K.1    Toda, F.2
  • 16
    • 0344731238 scopus 로고    scopus 로고
    • Lithium chloride catalysed acetylation of alcohols, thiols, phenols and amines
    • (a) Sabitha, G.; Reddy, B. V. S.; Srividya, R.; Yadav, R. S. Lithium chloride catalysed acetylation of alcohols, thiols, phenols and amines. Synth. Commun. 1999, 29, 2311-2315;
    • (1999) Synth. Commun. , vol.29 , pp. 2311-2315
    • Sabitha, G.1    Reddy, B.V.S.2    Srividya, R.3    Yadav, R.S.4
  • 17
    • 0001826395 scopus 로고
    • Synthesis of allylic halides and 1,5-dienes from allylic alcohols
    • (b) Stork, G.; Grieco, P. A.; Gregson, M. Synthesis of allylic halides and 1,5-dienes from allylic alcohols. Tetrahedron Lett. 1969, 1393-1395;
    • (1969) Tetrahedron Lett. , pp. 1393-1395
    • Stork, G.1    Grieco, P.A.2    Gregson, M.3
  • 18
    • 0008582242 scopus 로고
    • Dehydrobromination of 1,2-dibromo-cyclohexane and related compounds by lithium carbonate in hexamethylphosphorictriamide. An improved synthesis of 1,3-cyclohexadiene and some deuterium labeled analogs
    • (c) Weisz, A.; Mandelbaum, A. Dehydrobromination of 1,2-dibromo- cyclohexane and related compounds by lithium carbonate in hexamethylphosphorictriamide. An improved synthesis of 1,3-cyclohexadiene and some deuterium labeled analogs. J. Org. Chem. 1984, 49, 2648-2650;
    • (1984) J. Org. Chem. , vol.49 , pp. 2648-2650
    • Weisz, A.1    Mandelbaum, A.2
  • 19
    • 0000416631 scopus 로고    scopus 로고
    • A mild and efficient method for selective deprotection of tetrahydropyranyl ethers to alcohols
    • (d) Maiti, G.; Roy, S. C. A mild and efficient method for selective deprotection of tetrahydropyranyl ethers to alcohols. J. Org. Chem. 1996, 61, 6038-6039;
    • (1996) J. Org. Chem. , vol.61 , pp. 6038-6039
    • Maiti, G.1    Roy, S.C.2
  • 20
    • 0025896528 scopus 로고
    • A highly regioselective conversion of epoxides to halohydrins by lithium halides
    • (e) Bajwa, J. S.; Anderson, R. C. A highly regioselective conversion of epoxides to halohydrins by lithium halides. Tetrahedron Lett. 1991, 32, 3021-3024.
    • (1991) Tetrahedron Lett. , vol.32 , pp. 3021-3024
    • Bajwa, J.S.1    Anderson, R.C.2
  • 21
    • 0242384183 scopus 로고    scopus 로고
    • 4 catalysed conversion of aldehydes to geminal diacetates and dipivolates and their cleavage
    • 4 catalysed conversion of aldehydes to geminal diacetates and dipivolates and their cleavage. Tetrahedron 2003, 59, 9171-9576.
    • (2003) Tetrahedron , vol.59 , pp. 9171-9576
    • Smitha, G.1    Reddy, C.S.2
  • 22
    • 2442656516 scopus 로고    scopus 로고
    • An efficient and practical procedure for synthesis of 1,1-diacetates from aldehydes catalysed by zirconium sulphate tetrahydrate-silica gel
    • Jin, T.; Feng, G.; Yang, M.; Li, T. An efficient and practical procedure for synthesis of 1,1-diacetates from aldehydes catalysed by zirconium sulphate tetrahydrate-silica gel. Synth. Commun. 2004, 34, 1645-1651.
    • (2004) Synth. Commun. , vol.34 , pp. 1645-1651
    • Jin, T.1    Feng, G.2    Yang, M.3    Li, T.4
  • 23
    • 0037659792 scopus 로고    scopus 로고
    • Metal cation exchanged montmorillonite catalysed protection of aromatic aldehydes with acetic anhydride
    • Jankovic, L.; Komadel, P. Metal cation exchanged montmorillonite catalysed protection of aromatic aldehydes with acetic anhydride. J. Cat. 2003, 218, 227-233.
    • (2003) J. Cat. , vol.218 , pp. 227-233
    • Jankovic, L.1    Komadel, P.2
  • 25
    • 1842637247 scopus 로고    scopus 로고
    • Zinc-metal promoted selective α-haloacylation and gem-bisacylation of alkyl aldehydes in the presence of chlorotrimethylsilane
    • Ishino, Y.; Mihara, M.; Takeuchi, T.; Takemoto, M. Zinc-metal promoted selective α-haloacylation and gem-bisacylation of alkyl aldehydes in the presence of chlorotrimethylsilane. Tetrahedron Lett. 2004, 45, 3503-3506.
    • (2004) Tetrahedron Lett. , vol.45 , pp. 3503-3506
    • Ishino, Y.1    Mihara, M.2    Takeuchi, T.3    Takemoto, M.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.