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Volumn 27, Issue 5, 2008, Pages 484-494

Bicyclic nucleoside synthesis - A photochemical approach

Author keywords

Bicyclic nucleosides; Photolysis; Ring expansion; Synthesis

Indexed keywords

2 OXA BICYCLO[3.2.0]HEPTAN 6 ONE; 2 OXABICYCLO[4.2.0]OCTAN 7 ONE; 6 CHLORO 9 (HEXAHYDRO 2H FURO[3.2 B]PYRAN 2 YL) 9H PURINE; 6 CHLORO 9 (HEXAHYDROCYCLOPENTA[B]FURAN 2 YL) 9H PURINE; 6 CHLORO 9 (HEXAHYDROFURO[3,2 B]FURAN 2 YL) 9H PURINE; 6 CHLORO 9 (OCTAHYDROBENZOFURAN 2 YL) 9H PURINE; 7,7 DICHLORO 2 OXA BICYCLO[3.2.0]HEPTAN 6 ONE; 8,8 DICHLORO 2 OXABICYCLO[4.2.0]OCTAN 7 ONE; 8,8 DICHLOROBICYCLO[4.2.0]OCTAN 7 ONE; BICYCLO[3.2.0]HEPTAN 6 ONE; BICYCLO[4.2.0]OCTAN 7 ONE; CYCLOBUTANONE DERIVATIVE;

EID: 45849096108     PISSN: 15257770     EISSN: 15322335     Source Type: Journal    
DOI: 10.1080/15257770802088886     Document Type: Article
Times cited : (8)

References (15)
  • 1
    • 0001120760 scopus 로고    scopus 로고
    • Design principles for improving nucleic acid recognition by synthetic oligonucleotides
    • Kool, E.T. Preorganization of DNA: Design principles for improving nucleic acid recognition by synthetic oligonucleotides. Chem. Rev. 1997, 97, 1473-1488.
    • (1997) Chem. Rev , vol.97 , pp. 1473-1488
    • Kool, E.T.1    Preorganization of, D.N.A.2
  • 3
    • 0036169162 scopus 로고    scopus 로고
    • Leumann, C. DNA Analogues: From supramolecular principles to biological properties. Bioorg. Med. Chem. 2002, 10, 841-854.
    • Leumann, C. DNA Analogues: From supramolecular principles to biological properties. Bioorg. Med. Chem. 2002, 10, 841-854.
  • 4
    • 33947092205 scopus 로고
    • Extreme conformational flexibility of furanose ring in DNA and RNA
    • Levitt, M.; Warshel, A. Extreme conformational flexibility of furanose ring in DNA and RNA. J. Am. Chem. Soc. 1978, 100, 2607-2613.
    • (1978) J. Am. Chem. Soc , vol.100 , pp. 2607-2613
    • Levitt, M.1    Warshel, A.2
  • 6
    • 0019923858 scopus 로고
    • How Flexible is the Furanose Ring? 1. A comparison of experimental and theoretical studies
    • Olson, W.K. How Flexible is the Furanose Ring? 1. A comparison of experimental and theoretical studies. J. Am. Chem. Soc. 1982, 104, 278-286.
    • (1982) J. Am. Chem. Soc , vol.104 , pp. 278-286
    • Olson, W.K.1
  • 8
    • 0034607840 scopus 로고    scopus 로고
    • Synthesis of novel nucleosides with a fused cyclopropane ring substituted by a hydroxymethyl group
    • Lescop, C.; Huet, F. Synthesis of novel nucleosides with a fused cyclopropane ring substituted by a hydroxymethyl group. Tetrahedron 2000, 56, 2995-3003.
    • (2000) Tetrahedron , vol.56 , pp. 2995-3003
    • Lescop, C.1    Huet, F.2
  • 9
    • 33748711218 scopus 로고    scopus 로고
    • Aubin, Y.; Audran, G.; Monti, H. Conformationally locked carbocyclic nucleosides: synthesis of the 1-methyl-6-oxabicyclo[3.1.0]hexane scaffold. Synlett. 2006, 14, 2215-2219.
    • Aubin, Y.; Audran, G.; Monti, H. Conformationally locked carbocyclic nucleosides: synthesis of the 1-methyl-6-oxabicyclo[3.1.0]hexane scaffold. Synlett. 2006, 14, 2215-2219.
  • 10
    • 33749122260 scopus 로고    scopus 로고
    • Analogues of a locked nucleic acid with three-carbon 2′-4′-linkages: Synthesis by ring-closing metathesis and influence on nucleic acid duplex stability and structure
    • Albaek, N.; Peterson, M.; Nielson, P. Analogues of a locked nucleic acid with three-carbon 2′-4′-linkages: Synthesis by ring-closing metathesis and influence on nucleic acid duplex stability and structure. J. Org. Chem. 2006, 71, 7731-7740.
    • (2006) J. Org. Chem , vol.71 , pp. 7731-7740
    • Albaek, N.1    Peterson, M.2    Nielson, P.3
  • 11
    • 0031139312 scopus 로고    scopus 로고
    • Photodecarbonylation of chiral cyclobutanones
    • Ramnauth, J.; Lee-Ruff, E. Photodecarbonylation of chiral cyclobutanones. Can. J. Chem. 1997, 75, 518-535.
    • (1997) Can. J. Chem , vol.75 , pp. 518-535
    • Ramnauth, J.1    Lee-Ruff, E.2
  • 12
    • 33646533982 scopus 로고
    • Halogenated ketenes. XVI. Steric control in unsymmetrical ketene-olefin cycloadditions
    • Brady, W.T.; Roe, R. Halogenated ketenes. XVI. Steric control in unsymmetrical ketene-olefin cycloadditions. J. Am. Chem. Soc. 1971, 93, 1662-1664.
    • (1971) J. Am. Chem. Soc , vol.93 , pp. 1662-1664
    • Brady, W.T.1    Roe, R.2
  • 13
    • 0035112418 scopus 로고    scopus 로고
    • Preparation of TADOOH, a hydroperoxide from TADDOL, and use in highly enantioface- and enantiomer-differentiating oxidations
    • Aoki, M.; Seebach, D. Preparation of TADOOH, a hydroperoxide from TADDOL, and use in highly enantioface- and enantiomer-differentiating oxidations. Helv. Chim. Acta 2001, 84, 187-207.
    • (2001) Helv. Chim. Acta , vol.84 , pp. 187-207
    • Aoki, M.1    Seebach, D.2
  • 14
    • 0027318206 scopus 로고
    • Microbiological Transformations. 25. Enantioselective Baeyer-Villiger oxidation as a tool for the synthesis of enantiopure bicyclic furofuran and pyrofuran chirons
    • Petit, F.; Furstoss, R. Microbiological Transformations. 25. Enantioselective Baeyer-Villiger oxidation as a tool for the synthesis of enantiopure bicyclic furofuran and pyrofuran chirons. Tetrahedron Asymmetry 1993, 4, 1341-1352.
    • (1993) Tetrahedron Asymmetry , vol.4 , pp. 1341-1352
    • Petit, F.1    Furstoss, R.2
  • 15
    • 0342593711 scopus 로고
    • Preparation of Unsaturated α,α- dichloro acid chlorides and intramolecular [2+2] cycloadditions of the α-chloroketenes reductively generated from them. Effect of double bond geometry of the cycloaddition
    • Snider, B.B.; Walner, M. Preparation of Unsaturated α,α- dichloro acid chlorides and intramolecular [2+2] cycloadditions of the α-chloroketenes reductively generated from them. Effect of double bond geometry of the cycloaddition. Tetrahedron 1989, 45, 3171-3182.
    • (1989) Tetrahedron , vol.45 , pp. 3171-3182
    • Snider, B.B.1    Walner, M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.