SCOPUS 정보 검색 플랫폼

Volumn 26, Issue 10, 1985, Pages 1305-1306

One pot solid phase cleavage of alpha-diols to primary alcohols. An attractive route to trihydroxy-nucleosides, antiviral precursors.

(2) Bessodes, M a Antonakis, K a

a Institut de Recherches Scientifiques sur le Cancer (France)

Author keywords

[No Author keywords available]

Indexed keywords

1 [2 HYDROXY 1,1 BIS(HYDROXYMETHOXY)ETHOXY]CYTOSINE; 1 [2 HYDROXY 1,1 BIS(HYDROXYMETHOXY)ETHOXY]URACIL; 9 [2 HYDROXY 1,1 BIS(HYDROXYMETHOXY)ETHOXY]ADENINE; 9 [2 HYDROXY 1,1 BIS(HYDROXYMETHOXY)ETHOXY]GUANINE; DRUG ANALYSIS; DRUG IDENTIFICATION; DRUG SYNTHESIS; METHODOLOGY; NONHUMAN; NUCLEAR MAGNETIC RESONANCE; PRELIMINARY COMMUNICATION; PRIORITY JOURNAL; THEORETICAL STUDY;

EID: 0021923298 PISSN: 00404039 EISSN: None Source Type: Journal
DOI: 10.1016/S0040-4039(00)94877-9 Document Type: Article

Times cited : (44)

References (16)

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- Reaction times were in the range of 2 to 10 hours depending on the solubility of the compounds and the pump flow rate.

16
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- 2,OCH), 4.2–5.0 (bm, 4H:30H,NH), 5.65.7 (d,1H:H6, t,1H:NCH), 7.6 (d,1H:H5).AcOD was used to identify exchangeable protons. Other physical data 4a–d were in agreement with the literature.

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