Matches in SemOpenAlex for { <https://semopenalex.org/work/W1973966730> ?p ?o ?g. }
Showing items 1 to 91 of
91
with 100 items per page.
- W1973966730 endingPage "21" @default.
- W1973966730 startingPage "11" @default.
- W1973966730 abstract "X-ray crystallographic analyses are reported for the two title compounds (8 and 9, of which the former crystallized in two modifications (8a and 8b). In all three structures, the pyranose rings have the 4C1 (d) conformation and the substituents at C-1 are axial and those at C-2–C-4 are equatorial. The phenyl rings are oriented equatorially with their planes nearly parallel to the axial P = R bond (R = O, S). The favored conformations of various PhP(= R)-in-ring d-xylopyranose acetates (R =O,S, lone-pair; 8–19) in solution are discussed. The inclination of the equatorial P-phenyl group of the α- and β-d-xylopyranose analogs 8–13 is similar to that observed in the solid, whereas the inclination of the axial phenyl ring of the P-5 epimers 14–19 is near 90° with respect to the equatorial P = R bond." @default.
- W1973966730 created "2016-06-24" @default.
- W1973966730 creator A5010613960 @default.
- W1973966730 creator A5015432645 @default.
- W1973966730 creator A5059450534 @default.
- W1973966730 creator A5060011936 @default.
- W1973966730 date "1991-12-01" @default.
- W1973966730 modified "2023-09-28" @default.
- W1973966730 title "X-ray crystal structures of 1,2,4-tri-O-acetyl-5-deoxy-3-O-methyl-5-[(S)-phenylphosphinyl]-α-d-xylopyranose and its 5-[(S-phenylphosphinothioyl] derivative, and conformations of d-xylopyranose analogs having a C6H5P(=R) group in the hemiacetal ring" @default.
- W1973966730 cites W1000484957 @default.
- W1973966730 cites W1966661180 @default.
- W1973966730 cites W1976840161 @default.
- W1973966730 cites W1977340591 @default.
- W1973966730 cites W1997946412 @default.
- W1973966730 cites W2010490973 @default.
- W1973966730 cites W2020745804 @default.
- W1973966730 cites W2042216329 @default.
- W1973966730 cites W2052866801 @default.
- W1973966730 cites W2059133520 @default.
- W1973966730 cites W2068458601 @default.
- W1973966730 cites W2069309218 @default.
- W1973966730 cites W2073626169 @default.
- W1973966730 cites W2084483462 @default.
- W1973966730 cites W2093739306 @default.
- W1973966730 cites W2331572089 @default.
- W1973966730 doi "https://doi.org/10.1016/0008-6215(91)89002-w" @default.
- W1973966730 hasPublicationYear "1991" @default.
- W1973966730 type Work @default.
- W1973966730 sameAs 1973966730 @default.
- W1973966730 citedByCount "3" @default.
- W1973966730 crossrefType "journal-article" @default.
- W1973966730 hasAuthorship W1973966730A5010613960 @default.
- W1973966730 hasAuthorship W1973966730A5015432645 @default.
- W1973966730 hasAuthorship W1973966730A5059450534 @default.
- W1973966730 hasAuthorship W1973966730A5060011936 @default.
- W1973966730 hasConcept C106159729 @default.
- W1973966730 hasConcept C111771559 @default.
- W1973966730 hasConcept C112887158 @default.
- W1973966730 hasConcept C115624301 @default.
- W1973966730 hasConcept C120665830 @default.
- W1973966730 hasConcept C121332964 @default.
- W1973966730 hasConcept C162324750 @default.
- W1973966730 hasConcept C178790620 @default.
- W1973966730 hasConcept C185592680 @default.
- W1973966730 hasConcept C203130289 @default.
- W1973966730 hasConcept C207114421 @default.
- W1973966730 hasConcept C2780378348 @default.
- W1973966730 hasConcept C32909587 @default.
- W1973966730 hasConcept C34490408 @default.
- W1973966730 hasConcept C50515024 @default.
- W1973966730 hasConcept C6652555 @default.
- W1973966730 hasConcept C71240020 @default.
- W1973966730 hasConcept C8010536 @default.
- W1973966730 hasConceptScore W1973966730C106159729 @default.
- W1973966730 hasConceptScore W1973966730C111771559 @default.
- W1973966730 hasConceptScore W1973966730C112887158 @default.
- W1973966730 hasConceptScore W1973966730C115624301 @default.
- W1973966730 hasConceptScore W1973966730C120665830 @default.
- W1973966730 hasConceptScore W1973966730C121332964 @default.
- W1973966730 hasConceptScore W1973966730C162324750 @default.
- W1973966730 hasConceptScore W1973966730C178790620 @default.
- W1973966730 hasConceptScore W1973966730C185592680 @default.
- W1973966730 hasConceptScore W1973966730C203130289 @default.
- W1973966730 hasConceptScore W1973966730C207114421 @default.
- W1973966730 hasConceptScore W1973966730C2780378348 @default.
- W1973966730 hasConceptScore W1973966730C32909587 @default.
- W1973966730 hasConceptScore W1973966730C34490408 @default.
- W1973966730 hasConceptScore W1973966730C50515024 @default.
- W1973966730 hasConceptScore W1973966730C6652555 @default.
- W1973966730 hasConceptScore W1973966730C71240020 @default.
- W1973966730 hasConceptScore W1973966730C8010536 @default.
- W1973966730 hasLocation W19739667301 @default.
- W1973966730 hasOpenAccess W1973966730 @default.
- W1973966730 hasPrimaryLocation W19739667301 @default.
- W1973966730 hasRelatedWork W1981967761 @default.
- W1973966730 hasRelatedWork W1993702781 @default.
- W1973966730 hasRelatedWork W2003049472 @default.
- W1973966730 hasRelatedWork W2005445215 @default.
- W1973966730 hasRelatedWork W2006217345 @default.
- W1973966730 hasRelatedWork W2061751884 @default.
- W1973966730 hasRelatedWork W2063401985 @default.
- W1973966730 hasRelatedWork W2063731121 @default.
- W1973966730 hasRelatedWork W2075817299 @default.
- W1973966730 hasRelatedWork W2104602011 @default.
- W1973966730 hasVolume "222" @default.
- W1973966730 isParatext "false" @default.
- W1973966730 isRetracted "false" @default.
- W1973966730 magId "1973966730" @default.
- W1973966730 workType "article" @default.