About: Acyclonucleosides: Part 2. diseco-Nucleosides* * Part 1 is in Volume 67 and Part 3 is in Volume 69.

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About: Acyclonucleosides: Part 2. diseco-Nucleosides* * Part 1 is in Volume 67 and Part 3 is in Volume 69. Goto Sponge NotDistinct Permalink

An Entity of Type : schema:ScholarlyArticle, within Data Space : wasabi.inria.fr associated with source document(s)

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type	Academic Article research paper schema:ScholarlyArticle
isDefinedBy	Covid-on-the-Web dataset
title	Acyclonucleosides: Part 2. diseco-Nucleosides* * Part 1 is in Volume 67 and Part 3 is in Volume 69.
Creator	El Kilany, Y El, E
source	Elsevier; Medline; PMC
abstract	This chapter is the second of a sequence of three chapters that appears in successive volumes of this series dealing with the chemistry of acyclonucleosides. The first chapter appeared in the previous volume [97AHC391] and dealt with seco-nucleosides (one bond disconnection). This chapter deals with diseco-nucleosides (two bond disconnections). The final chapter of this series will deal with tri-, tetra-, and pentaseco-nucleosides, as well as contain an appendix of the literature that appeared after the three chapters were prepared.
has issue date	1997-12-31(xsd:dateTime)
bibo:doi	10.1016/s0065-2725(08)60360-8
bibo:pmid	32287460
has license	els-covid
sha1sum (hex)	19081638ded340084d85b73b78b49d1c67de386f
schema:url	https://doi.org/10.1016/s0065-2725%2808%2960360-8
resource representing a document's title	Acyclonucleosides: Part 2. diseco-Nucleosides* * Part 1 is in Volume 67 and Part 3 is in Volume 69.
has PubMed Central identifier	PMC7112104
has PubMed identifier	32287460
schema:publication	Advances in Heterocyclic Chemistry
resource representing a document's body	covid:19081638ded340084d85b73b78b49d1c67de386f#body_text
is schema:about of	named entity 'VOL' named entity 'CHEMISTRY' named entity 'NUCLEOSIDES' named entity 'acyclovir' named entity 'ethoxy group' named entity 'CBr4' named entity 'flUOrO' named entity 'fluoro' named entity 'antiviral activity' named entity 'boron trichloride' named entity 'diol' named entity 'tosylation' named entity 'phthalic anhydride' named entity 'chlorobenzene' named entity 'fluorination' named entity 'hydroxylated' named entity '1,2-dichloroethane' named entity 'hydantoin' named entity 'hydrogenated' named entity 'oxygen' named entity 'deprotection' named entity 'condensation' named entity 'N-9' named entity 'heterocyclic rings' named entity 'carbonyl' named entity 'charcoal' named entity 'optically pure' named entity 'nitrite' named entity 'benzotriazole' named entity 'deacetylated' named entity 'iodine' named entity 'pyrimidine' named entity 'AZT' named entity 'uracil' named entity 'chlorine' named entity 'Chloromethylation' named entity 'similar manner' named entity 'deacetylation' named entity 'alkylation' named entity 'acetal' named entity 'Acid hydrolysis' named entity 'trans' named entity 'amino group' named entity 'silylated' named entity 'cytidine' named entity 'chromatography' named entity 'guanidine' named entity 'hydrochloric acid' named entity 'adduct' named entity 'diazotized' named entity 'adenine' named entity 'cytidine' named entity 'colon' named entity 'D-mannitol' named entity 'deprotection' named entity 'mesylation' named entity 'pyrimidine' named entity 'dioxolanes' named entity 'purine' named entity 'isomers' named entity 'toxicity' named entity 'ether' named entity 'dioxolane' named entity 'alkylation' named entity 'acetyl group' named entity 'functional group' named entity 'benzyl' named entity 'unsaturated' named entity 'dihexanoate' named entity 'analog' named entity 'oxide' named entity 'alkylation' named entity 'ethers' named entity 'benzyl' named entity 'benzyl groups' named entity 'deprotection' named entity 'SN2 substitution' named entity 'catalytic hydrogenation' named entity 'trans-esterification' named entity 'Condensation'

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