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Volumn 63, Issue 24, 2007, Pages 5274-5286

Corrigendum to "Synthesis and reactivity of (RS)-6-chloro-7- or 9-(1,2,3,5-tetrahydro-4,1-benzoxazepin-3-yl)-7H- or 9H-purines bearing a nitrobenzenesulfonyl group on the nitrogen atom". [Tetrahedron 63 (2007) 5274] (DOI:10.1016/j.tet.2007.03.155);Synthesis and reactivity of (RS)-6-chloro-7- or 9-(1,2,3,5-tetrahydro-4,1-benzoxazepin-3-yl)-7H- or 9H-purines bearing a nitrobenzenesulfonyl group on the nitrogen atom

Author keywords

Acetals; Benzoxazepines; Medium ring heterocycles; Purines; X ray

Indexed keywords

3 METHOXY 1 [(2) NITROBENZENESULFONYL)] 1,2,3,5 TETRAHYDRO 4,1 BENZOXAZEPINE; 3 METHOXY 1 [(4) NITROBENZENESULFONYL)] 1,2,3,5 TETRAHYDRO 4,1 BENZOXAZEPINE; 6 CHLORO 7 (1,2,3,5 TETRAHYDRO 4,1 BENZOXAZEPIN 3 YL) 7H PURINE; 6 CHLORO 9 (1,2,3,5 TETRAHYDRO 4,1 BENZOXAZEPIN 3 YL) 9H PURINE; 6 CHLOROPURINE; BENZENE DERIVATIVE; CARBAMIC ACID; DIMETHYL SULFOXIDE; FLUOROURACIL; HYDROXYL GROUP; LEWIS ACID; NITROGEN; PURINE DERIVATIVE; PYRIMIDINE DERIVATIVE; SULFONAMIDE; THIOPHENOL; UNCLASSIFIED DRUG; URACIL;

EID: 34247866205     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2007.06.035     Document Type: Erratum
Times cited : (8)

References (34)
  • 3
    • 0037714410 scopus 로고    scopus 로고
    • Synthesis of Nucleosides
    • Paquette L.A. (Ed), John Wiley and Sons, New York, NY
    • Vorbrüggen H., and Ruh-Pohlenz C. Synthesis of Nucleosides. In: Paquette L.A. (Ed). Organic Reactions (New York) Vol. 55 (2000), John Wiley and Sons, New York, NY 1-630
    • (2000) Organic Reactions (New York) , vol.55 , pp. 1-630
    • Vorbrüggen, H.1    Ruh-Pohlenz, C.2
  • 9
    • 0023890847 scopus 로고
    • 4 and MeCN at rt, while the N-9 alkylated products were obtained with the same purines, but using TMSOTf and refluxing 1,2-dichloroethane as solvent
    • 4 and MeCN at rt, while the N-9 alkylated products were obtained with the same purines, but using TMSOTf and refluxing 1,2-dichloroethane as solvent
    • (1988) J. Org. Chem. , vol.53 , pp. 1294
    • Garner, P.1    Ramakanth, S.2
  • 13
    • 34247866749 scopus 로고    scopus 로고
    • note
    • 1 group are numbered with primes (′), while the purine bases are numbered with double primes (″).
  • 18
    • 34247871683 scopus 로고    scopus 로고
    • note
    • Isomer's identification has been made from the value of the coupling constant between the olefinic hydrogens in each structure.
  • 25
    • 34247844791 scopus 로고    scopus 로고
    • 3 allows the nucleophile attack at the position 6, in DMF, see: Gurvich, V.; Kim, H. Y.; Hodge, R. P.; Harris, C. M.; Harris, T. M. Abstracts of Papers, 218th ACS National Meeting, New Orleans, 1999.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.