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Volumn 35, Issue 23, 1994, Pages 4019-4022

Total syntheses of N-boc-protected 3′-deoxy-4′-azathymidine and 4′-azauridine

Author keywords

[No Author keywords available]

Indexed keywords

4' AZATHYMIDINE DERIVATIVE; 4' AZAURIDINE DERIVATIVE; THYMIDINE DERIVATIVE; UNCLASSIFIED DRUG; URIDINE DERIVATIVE;

EID: 0028264490     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)76729-3     Document Type: Article
Times cited : (49)

References (33)
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    • (1993) Tetrahedron , vol.49 , pp. 9877-9936
    • Wnuk1
  • 17
    • 0022613143 scopus 로고
    • Inhibitors of purine nucleoside phosphorylase: effects of 9-deazapurine ribonucleosides and synthesis of 5'-deoxy-5'-iodo-9-deazainosine.
    • (1986) Cancer Res , vol.46 , pp. 1774-1778
    • Stoeckler1    Ryden2    Parks3    Chu4    Lim5    Ren6    Klein7
  • 20
    • 0027383437 scopus 로고
    • Pyrrolidine based analogs of 3′-deoxythymidine
    • Just prior to submission of this manuscript, we became aware of an approach to pyrrolidine-based analogs of 3′-deoxythymidine which utilizes (S)-pyroglutamic acid,in a fashion which is complementary to our procedure. See
    • (1993) Tetrahedron Letters , vol.34 , pp. 7721-7724
    • Altmann1
  • 21
    • 0027524581 scopus 로고
    • A new class of C-nucleoside analogues. 1-(S)-aryl-1,4-dideoxy-1,4-imino-D-ribitols, transition state analogue inhibitors of nucleoside hydrolase
    • C-Nucleoside analogues
    • (1993) Tetrahedron Letters , vol.34 , pp. 7213-7216
    • Horenstein1    Zabinski2    Schramm3
  • 24
    • 84912908702 scopus 로고    scopus 로고
    • 4/MeOH resulted in extensive opening of the lactam ring.
  • 25
    • 84912911159 scopus 로고    scopus 로고
    • 4: C, 55.51; H, 6.81; N, 14.94. Found: C, 55.44; H, 6.89; N, 15.00.
  • 28
    • 84912924185 scopus 로고    scopus 로고
    • 5: C, 55.37; H, 7.13; N, 12.91. Found: C, 55.48; H, 7.20; N, 12.98.
  • 29
    • 84912920512 scopus 로고    scopus 로고
    • 5: C, 55.37; H, 7.13; N, 12.91. Found: C, 55.43; H, 7.25; N, 13.00.
  • 30
    • 0025985753 scopus 로고
    • Asymmetric synthesis from α-amino acids; some reactions of (S)-pyroglutamate
    • (1991) Tetrahedron Letters , vol.32 , pp. 6949-6952
    • Woo1    Jones2
  • 32
    • 0001078307 scopus 로고
    • 4-O-Benzyl-23-O-isopropylidene-L-threose: A useful building block for stereoselective synthesis of monosaccharides
    • (1990) Tetrahedron , vol.46 , pp. 265-276
    • Mukaiyama1    Suzuki2    Yamada3    Tabusa4
  • 33
    • 84912896712 scopus 로고    scopus 로고
    • 7: C, 48.98; H, 6.17; N, 12.24. Found: C, 49.11; H, 6.31; N, 12.06.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.