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Antiviral Activity of Oxetanocins against Varicella-Zoster Virus
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0024262556
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Synthesis and Antihepetic Activity of (±)-9-[(Z)-2-Hydroxymethylcyclopropyl]methylguanine and Related Compounds
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Ashton, W. T.; Meurer, L. C.; Cantone, C. L.; Field, A. K.; Hannah, J.; Karkas, J. D.; Liou, R.; Patel, G. F.; Perry, H. C.; Wager, A. F.; Walton, E.; Tolman, R. L. Synthesis and Antihepetic Activity of (±)-9-[(Z)-2-Hydroxymethyl)cyclopropyl]methyl]guanine and Related Compounds. J. Med. Chem. 1988, 31, 2304-2315.
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19
-
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15444355766
-
-
The vicinal coupling constants between C1 and C2 protons of the cyclopropane ring are 8.06 Hz for 8 (all-cis) and 4.64 Hz for 9, respectively
-
The vicinal coupling constants between C1 and C2 protons of the cyclopropane ring are 8.06 Hz for 8 (all-cis) and 4.64 Hz for 9, respectively.
-
-
-
-
20
-
-
15444347658
-
-
NOE was observed between the methylene protons of 1-hydroxymethyl and the methylene protons of 2-(benzoyloxy)methyl
-
NOE was observed between the methylene protons of 1-hydroxymethyl and the methylene protons of 2-(benzoyloxy)methyl.
-
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-
21
-
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0001155545
-
A New Method for the Stereocontrolled Synthesis of Silyldienol Ether Using (Naphthalene) Chromium Tricarbonyl Catalyzed Isomerization
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15444342087
-
-
NOE was observed between the olefmic proton and the methylene protons adjacent to the purine ring in Z-olefin 31 and the protected forms of 40d and 41d
-
NOE was observed between the olefmic proton and the methylene protons adjacent to the purine ring in Z-olefin 31 and the protected forms of 40d and 41d.
-
-
-
-
23
-
-
15444352975
-
-
The stereochemistry of 36 was confirmed by identity with the compound synthesized from (E)-29a in a separate run
-
The stereochemistry of 36 was confirmed by identity with the compound synthesized from (E)-29a in a separate run.
-
-
-
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24
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0024438946
-
Synthesis and Study of Racemic, (1R,2S)-, and (1S,2R)-1-Amino-2-(hydroxymethyl)-cyclopropane Carboxylic Acid
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25
-
-
15444345076
-
-
note
-
Since it is reported in ref 14 that condensation of diethyl malonate and epichlorohydrin proceeds by sequential alkylations with inversion of stereochemistry, the absolute configuration of the cyclopropane lactone prepared from (R)-(-)-epichlorohydrin should be that of 47. To confirm the stereochemistry, 4-bro- mophenacyl ester of 47 was prepared and the absolute structure was determined by X-ray crystallography. Since there is no chance of racemization in the preparation of 3a from 47, the absolute conformation of 3a prepared from (R)-(-)-epichlorohydrin is 1′S,2′R.
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26
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0021039002
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0017143385
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Synthesis and Anti-HIV Activity of 9-[c-4,t-5-Bis(hydroxymethyl)cyclopent-2-en-r-1-yl]-9H-adenine
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Inhibition of Purified Human and Herpes Simplex Virus-induced DNA Polymerases by 9-(2-hydroxyethoxymethyl)guanine Triphosphate
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Derse, D.; Cheng, Y.-C.; Furman, P. A.; St. Char, M. H.; Elion, G. B. Inhibition of Purified Human and Herpes Simplex Virus-induced DNA Polymerases by 9-(2-hydroxyethoxymethyl)guanine Triphosphate. J. Biol. Chem. 1957, 67, 602-610.
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0025364142
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