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Volumn 47, Issue 15, 2006, Pages 2501-2505

Highly chemo- and regioselective phosphitylation of unprotected 2′-deoxyribonucleosides

Author keywords

Nucleic acids; Nucleotides; Phosphitylation; Phosphoramidite

Indexed keywords

2 N DIMETHOXYTRITYL 2' DEOXYGUANOSINE 5' DI TERT BUTYL PHOSPHITE; 2' DEOXYADENOSINE 5' DI TERT BUTYL PHOSPHITE; 2' DEOXYCYTIDINE 5' DI TERT BUTYL PHOSPHITE; 2' DEOXYGUANOSINE 5' DI TERT BUTYL PHOSPHITE; 2' DEOXYRIBONUCLEOSIDE 5' PHOSPHITE DERIVATIVE; 4 N DIMETHOXYTRITYL 2' DEOXYCYTIDINE 5' DI TERT BUTYL PHOSPHITE; DEOXYRIBONUCLEOSIDE; DI TERT BUTYL N,N DIETHYLPHOSPHORAMIDITE; HYDROXYL GROUP; PHOSPHITE; PHOSPHORAMIDOUS ACID DERIVATIVE; THYMIDINE 5' DI TERT BUTYL PHOSPHITE; THYMIDINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 33644885723     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2006.02.060     Document Type: Article
Times cited : (6)

References (28)
  • 4
    • 0033689049 scopus 로고    scopus 로고
    • K. Burgess, and D. Cook Chem. Rev. 100 2000 2047 2059 and references cited therein
    • (2000) Chem. Rev. , vol.100 , pp. 2047-2059
    • Burgess, K.1    Cook, D.2
  • 23
    • 33644914624 scopus 로고    scopus 로고
    • note
    • 31P NMR.
  • 28
    • 33644893246 scopus 로고    scopus 로고
    • note
    • The moderate yields of these compounds would be attributed to the purification procedure, because the products are stable enough and the chemo- and regioselectivities of the reactions are sufficient. A part of the products were lost during the purification by crystallization or silica gel column chromatography.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.