The development of polyquinane chemistry
Identifieur interne : 001852 ( Istex/Curation ); précédent : 001851; suivant : 001853The development of polyquinane chemistry
Auteurs : Leo A. Paquette [États-Unis]Source :
- Topics in Current Chemistry [ 0340-1022 ]
Abstract
Abstract: Although various bicyclo[3.3.0]octane derivatives have been known for several decades, the chemistry of this ring system and the higher polyquinanes has developed particularly rapidly in the last decade. These developments have been stimulated by a wide range of interests and have encompassed a broad spectrum of research chemists. One may now safely claim that polyquinanes are readily available molecules. The more complex members of this class, particularly those endowed with all-cis stereo-chemistry, take on a “sphere-like” topology and conformational rigidity. As sphericality increases, the ability of a molecule to exclude solvation from its inner core is enhanced. Can smaller molecules or atoms be occluded therein? And what about completely enclosed structures such as the pentagonal dodecahedrane? What unique properties will characterize compounds of this type? It is the quest for such information that will propel the field of polyquinane chemistry rapidly forward in the years to come. The increasing complexity of natural products having multiply fused cyclopentanoid rings will generate a comparably high level of chemical investigation in this field.
Url:
DOI: 10.1007/BFb0048476
Links toward previous steps (curation, corpus...)
- to stream Istex, to step Corpus: Pour aller vers cette notice dans l'étape Curation :001852
Links to Exploration step
ISTEX:583565819DA458A14E32E32A3EAF72473A2AEC9ALe document en format XML
<record><TEI wicri:istexFullTextTei="biblStruct"><teiHeader><fileDesc><titleStmt><title xml:lang="en">The development of polyquinane chemistry</title><author><name sortKey="Paquette, Leo A" sort="Paquette, Leo A" uniqKey="Paquette L" first="Leo A." last="Paquette">Leo A. Paquette</name><affiliation wicri:level="1"><mods:affiliation>Evans Chemical Laboratories, The Ohio State University, 43210, Columbus, Ohio, USA</mods:affiliation><country xml:lang="fr">États-Unis</country><wicri:regionArea>Evans Chemical Laboratories, The Ohio State University, 43210, Columbus, Ohio</wicri:regionArea></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">ISTEX</idno><idno type="RBID">ISTEX:583565819DA458A14E32E32A3EAF72473A2AEC9A</idno><date when="1979" year="1979">1979</date><idno type="doi">10.1007/BFb0048476</idno><idno type="url">https://api.istex.fr/ark:/67375/HCB-X6BS0WWT-2/fulltext.pdf</idno><idno type="wicri:Area/Istex/Corpus">001852</idno><idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Corpus" wicri:corpus="ISTEX">001852</idno><idno type="wicri:Area/Istex/Curation">001852</idno></publicationStmt><sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">The development of polyquinane chemistry</title><author><name sortKey="Paquette, Leo A" sort="Paquette, Leo A" uniqKey="Paquette L" first="Leo A." last="Paquette">Leo A. Paquette</name><affiliation wicri:level="1"><mods:affiliation>Evans Chemical Laboratories, The Ohio State University, 43210, Columbus, Ohio, USA</mods:affiliation><country xml:lang="fr">États-Unis</country><wicri:regionArea>Evans Chemical Laboratories, The Ohio State University, 43210, Columbus, Ohio</wicri:regionArea></affiliation></author></analytic><monogr></monogr><series><title level="s" type="main" xml:lang="en">Topics in Current Chemistry</title><title level="s" type="abbrev">Top Curr Chem</title><idno type="ISSN">0340-1022</idno><idno type="eISSN">1436-5049</idno><idno type="ISSN">0340-1022</idno></series></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0340-1022</idno></seriesStmt></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Abstract: Although various bicyclo[3.3.0]octane derivatives have been known for several decades, the chemistry of this ring system and the higher polyquinanes has developed particularly rapidly in the last decade. These developments have been stimulated by a wide range of interests and have encompassed a broad spectrum of research chemists. One may now safely claim that polyquinanes are readily available molecules. The more complex members of this class, particularly those endowed with all-cis stereo-chemistry, take on a “sphere-like” topology and conformational rigidity. As sphericality increases, the ability of a molecule to exclude solvation from its inner core is enhanced. Can smaller molecules or atoms be occluded therein? And what about completely enclosed structures such as the pentagonal dodecahedrane? What unique properties will characterize compounds of this type? It is the quest for such information that will propel the field of polyquinane chemistry rapidly forward in the years to come. The increasing complexity of natural products having multiply fused cyclopentanoid rings will generate a comparably high level of chemical investigation in this field.</div></front></TEI></record>Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Sante/explor/H2N2V1/Data/Istex/Curation
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 001852 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Istex/Curation/biblio.hfd -nk 001852 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien
|wiki= Sante
|area= H2N2V1
|flux= Istex
|étape= Curation
|type= RBID
|clé= ISTEX:583565819DA458A14E32E32A3EAF72473A2AEC9A
|texte= The development of polyquinane chemistry
}}
| This area was generated with Dilib version V0.6.33. |  |