Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Vladimir Neschadimenko"'
Autor:
Chung Y Chen, Carl W. Fuller, Satyam Nampalli, Prasad Dhulipala, Shiv Kumar, Vladimir Neschadimenko, Jeffrey Wegener, Haiguang Xiao, Sudhakar Rao Takkellapati
Publikováno v:
Nucleosides, Nucleotides and Nucleic Acids. 26:1467-1470
Synthesis of aminomethyl and bis-aminomethylfluorescein derived energy transfer terminators is described.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9aed304b21f10d8ded24c41ad06c30c2
https://doi.org/10.1080/15257770701542579
https://doi.org/10.1080/15257770701542579
Autor:
Ronald T. Borchardt, Morris J. Robins, Stanislaw F. Wnuk, Vladimir Neschadimenko, Chong-Sheng Yuan, Bong-Oh Ro
Publikováno v:
The Journal of Organic Chemistry. 63:1205-1211
S-Adenosyl-l-homocysteine (AdoHcy) hydrolase is crucial for the maintenance of biomethylation. The usual mechanistic sequence involves oxidation of AdoHcy at C3‘ followed by elimination of l-homocysteine, Michael addition of water, and reduction to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::849793b889314132740b978a0fde6aac
https://doi.org/10.1021/jo971741u
https://doi.org/10.1021/jo971741u
Publikováno v:
Tetrahedron. 53:6295-6302
Sodium naphthalenide effects removal of 2′-, 3′-, or 5′-O-tosyl groups from the sugar, and 2-, 6-, or 8-halogens from purine nucleosides. An improved tosyl protection strategy was developed for the synthesis of 9-(3-deoxy-3-fluoro-β-D-xylofura
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fc938049acc0d0571004524c26255070
https://doi.org/10.1016/s0040-4020(97)00313-x
https://doi.org/10.1016/s0040-4020(97)00313-x
Publikováno v:
ChemInform. 28
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::13a9cbdec96c33cea1bb3ed051685806
https://doi.org/10.1002/chin.199738270
https://doi.org/10.1002/chin.199738270
Publikováno v:
The Journal of organic chemistry. 67(25)
Stereoselective pyramidalization of free radicals by a vicinal fluorine substituent, the beta-fluorine effect, was invoked to rationalize a 77:23 anti/syn ratio of 2-deuterio-1-fluorocyclopentanes obtained by radical reduction of trans-2-fluoro-1-bro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e1abc028bcdd2d2ddc92e0a84f84047
https://pubmed.ncbi.nlm.nih.gov/12467391
https://pubmed.ncbi.nlm.nih.gov/12467391