메뉴 건너뛰기




Volumn 34, Issue 13, 2004, Pages 2487-2498

Synthesis of 5-alkyl-2,3-dihydro-1,4-benzodioxins

Author keywords

2 Alkyl phenols; 5 Alkyl 2,3 dihydro 1,4 benzodioxins; Cyclization; Enzyme substrate complex

Indexed keywords

1,4 BENZODIOXIN DERIVATIVE; ALKYL GROUP; ALKYLPHENOL;

EID: 3543125455     PISSN: 00397911     EISSN: None     Source Type: Journal    
DOI: 10.1081/SCC-120039503     Document Type: Article
Times cited : (2)

References (14)
  • 1
    • 0342388131 scopus 로고
    • Ring-closure reactions. II. Kinetics of six- to ten-membered ring formation from o-ω-bromoalkoxy-phenoxides
    • Illuminati, G.; Mandolini, L.; Masci, B. Ring-closure reactions. II. Kinetics of six- to ten-membered ring formation from o-ω-bromoalkoxy- phenoxides. J. Am. Chem. Soc. 1974, 96 (5), 1422-1427.
    • (1974) J. Am. Chem. Soc. , vol.96 , Issue.5 , pp. 1422-1427
    • Illuminati, G.1    Mandolini, L.2    Masci, B.3
  • 2
    • 0342856432 scopus 로고
    • Ring-closure reactions. 19. Kinetics of formation of benzo-crown etheres by intramolecular nucleophilic substitution. A comparison between poly(oxyethylene) and polymethylene chains
    • Illuminati, G.; Mandolini, L.; Masci, B. Ring-closure reactions. 19. Kinetics of formation of benzo-crown etheres by intramolecular nucleophilic substitution. A comparison between poly(oxyethylene) and polymethylene chains. J. Am. Chem. Soc. 1981, 103 (14), 4142-4145.
    • (1981) J. Am. Chem. Soc. , vol.103 , Issue.14 , pp. 4142-4145
    • Illuminati, G.1    Mandolini, L.2    Masci, B.3
  • 3
    • 0011365215 scopus 로고
    • Ring-closure reactions. V. Kinetics of five- to ten-membered ring formation from o-ω-bromoalkyl-phenoxides. The influence of the O-heteroatom
    • Illuminati, G.; Mandolini, L.; Masci, B. Ring-closure reactions. V. Kinetics of five- to ten-membered ring formation from o-ω-bromoalkyl- phenoxides. The influence of the O-heteroatom. J. Am. Chem. Soc. 1975, 97 (17), 4960-4966.
    • (1975) J. Am. Chem. Soc. , vol.97 , Issue.17 , pp. 4960-4966
    • Illuminati, G.1    Mandolini, L.2    Masci, B.3
  • 4
    • 0000712253 scopus 로고
    • Ring-closure reactions. 9. Kinetics of ring formation from o-ω-bromoalkoxy phenoxides and o-ω-bromoalkyl phenoxides in the range of 11- to 24-membered rings. A comparison with related cyclization series
    • Illuminati, G.; Mandolini, L.; Masci, B. Ring-closure reactions. 9. Kinetics of ring formation from o-ω-bromoalkoxy phenoxides and o-ω-bromoalkyl phenoxides in the range of 11- to 24-membered rings. A comparison with related cyclization series. J. Am. Chem. Soc. 1977, 99 (19), 6308-6312.
    • (1977) J. Am. Chem. Soc. , vol.99 , Issue.19 , pp. 6308-6312
    • Illuminati, G.1    Mandolini, L.2    Masci, B.3
  • 6
    • 0000668077 scopus 로고
    • Surfactant effects upon cyclization of o-(ω-haloalkoxy)phenoxide ions. The role of premicellar assemblies
    • Cerichelli, G.; Mancini, G.; Luchetti, L.; Savelli, G.; Bunton, C.A. Surfactant effects upon cyclization of o-(ω-haloalkoxy)phenoxide ions. The role of premicellar assemblies. Langmuir 1994, 10 (11), 3982-3987.
    • (1994) Langmuir , vol.10 , Issue.11 , pp. 3982-3987
    • Cerichelli, G.1    Mancini, G.2    Luchetti, L.3    Savelli, G.4    Bunton, C.A.5
  • 8
    • 0015526361 scopus 로고
    • Stereopopulation control. II. Rate enhancement of intramolecular nucleophilic displacement
    • Borchardt, R.T.; Cohen, L.A. Stereopopulation control. II. Rate enhancement of intramolecular nucleophilic displacement. J. Am. Chem. Soc. 1972, 94 (26), 9166-9174.
    • (1972) J. Am. Chem. Soc. , vol.94 , Issue.26 , pp. 9166-9174
    • Borchardt, R.T.1    Cohen, L.A.2
  • 9
    • 0015526371 scopus 로고
    • Stereopopulation control. I. Rate enhancement in the lactonizations of o-hydroxyhydrocinnamic acids
    • Milstien, S.; Cohen, L.A. Stereopopulation control. I. Rate enhancement in the lactonizations of o-hydroxyhydrocinnamic acids. J. Am. Chem. Soc. 1972, 94 (26), 9158-9165.
    • (1972) J. Am. Chem. Soc. , vol.94 , Issue.26 , pp. 9158-9165
    • Milstien, S.1    Cohen, L.A.2
  • 10
    • 0033592820 scopus 로고    scopus 로고
    • Directed ortho metalation and Suzuki-Miyaura cross-coupling connections: Regiospecific synthesis of all isomeric chlorodihydroxybiphenyls for microbial degradation studes of PCBs
    • Nerdinger, S.; Kendall, C.; Marchhart, R.; Riebel, P.; Johnson, M.R.; Yin, C.-F.; Eltis, L.D.; Snieckus, V. Directed ortho metalation and Suzuki-Miyaura cross-coupling connections: Regiospecific synthesis of all isomeric chlorodihydroxybiphenyls for microbial degradation studes of PCBs. Chem. Commun. 1999, (22), 2259-2260.
    • (1999) Chem. Commun. , Issue.22 , pp. 2259-2260
    • Nerdinger, S.1    Kendall, C.2    Marchhart, R.3    Riebel, P.4    Johnson, M.R.5    Yin, C.-F.6    Eltis, L.D.7    Snieckus, V.8
  • 11
    • 0012397313 scopus 로고
    • Directed ortho metalation. Tertiary amide and O-carbamate directors in synthetic strategies for polysubstituted aromatics
    • Snieckus, V. Directed ortho metalation. Tertiary amide and O-carbamate directors in synthetic strategies for polysubstituted aromatics. Chem. Ver. 1990, 90, 879-933.
    • (1990) Chem. Ver. , vol.90 , pp. 879-933
    • Snieckus, V.1
  • 12
    • 0001311875 scopus 로고
    • Phenoxide-directed ortho lithiation
    • Posner, G.H.; Canella, K.A. Phenoxide-directed ortho lithiation. J. Am. Chem. Soc. 1985, 107 (8), 2571-2573.
    • (1985) J. Am. Chem. Soc. , vol.107 , Issue.8 , pp. 2571-2573
    • Posner, G.H.1    Canella, K.A.2
  • 13
    • 0008527723 scopus 로고
    • Directed hydroxylation of aromatics
    • Parker, K.A.; Koziski, K.A. Directed hydroxylation of aromatics. J. Org. Chem. 1987, 52 (4), 674-676.
    • (1987) J. Org. Chem. , vol.52 , Issue.4 , pp. 674-676
    • Parker, K.A.1    Koziski, K.A.2
  • 14
    • 3543053541 scopus 로고
    • The reaction of alkylcyclohexanones with copper(II) bromide and 1,2-glycols
    • Haruta, A.M.; Satoh, J.Y. The reaction of alkylcyclohexanones with copper(II) bromide and 1,2-glycols. Chem. Lett. 1980, 5, 473-476.
    • (1980) Chem. Lett. , vol.5 , pp. 473-476
    • Haruta, A.M.1    Satoh, J.Y.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.