ChemInform Abstract: A General Synthetic Approach to the (20S)‐Camptothecin Family of Antitumor Agents by a Regiocontrolled Cascade Radical Cyclization of Aryl Isonitriles.
Identifieur interne : 00B618 ( Main/Exploration ); précédent : 00B617; suivant : 00B619ChemInform Abstract: A General Synthetic Approach to the (20S)‐Camptothecin Family of Antitumor Agents by a Regiocontrolled Cascade Radical Cyclization of Aryl Isonitriles.
Auteurs : H. Josien [États-Unis] ; S. Ko [États-Unis] ; D. Bom [États-Unis] ; D. P. Curran [États-Unis]Source :
- ChemInform [ 0931-7597 ] ; 1998-04-14.
English descriptors
- KwdEn :
- Alkaloid, Alkylation, Antitumor, Antitumor agents, Aryl isonitriles, Camptothecin, Cascade, Chem, Curran, Cyclization, Dihydroxylation, Heck cyclization, Hexacyclic, Hexacyclic analogues, Iododesilylation, Isonitrile, Isonitriles, Josien, Lactol, Lactol oxidation, Lactone, Metalation, Metalation reactions, Multi, Multi substituents, Other penta, Penta, Propargylating, Propargylating agent, Pyridone, Reaction camptothecin, Regiocontrolled, Regiocontrolled cascade, Sharpless, Substituents, Title alkaloid, Univ.
- Teeft :
- Alkaloid, Alkylation, Antitumor, Antitumor agents, Aryl isonitriles, Camptothecin, Cascade, Chem, Curran, Cyclization, Dihydroxylation, Heck cyclization, Hexacyclic, Hexacyclic analogues, Iododesilylation, Isonitrile, Isonitriles, Josien, Lactol, Lactol oxidation, Lactone, Metalation, Metalation reactions, Multi, Multi substituents, Other penta, Penta, Propargylating, Propargylating agent, Pyridone, Reaction camptothecin, Regiocontrolled, Regiocontrolled cascade, Sharpless, Substituents, Title alkaloid, Univ.
Abstract
ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
Url:
DOI: 10.1002/chin.199815235
Affiliations:
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Le document en format XML
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Pittsburgh, Pittsburgh, PA 15260</wicri:regionArea><placeName><region type="state">Pennsylvanie</region></placeName></affiliation></author></analytic><monogr></monogr><series><title level="j" type="main">ChemInform</title><title level="j" type="alt">CHEMINFORM</title><idno type="ISSN">0931-7597</idno><idno type="eISSN">1522-2667</idno><imprint><biblScope unit="vol">29</biblScope><biblScope unit="issue">15</biblScope><biblScope unit="page" from="no">no</biblScope><biblScope unit="page" to="no">no</biblScope><biblScope unit="page-count">1</biblScope><publisher>WILEY‐VCH Verlag</publisher><pubPlace>Weinheim</pubPlace><date type="published" when="1998-04-14">1998-04-14</date></imprint><idno type="ISSN">0931-7597</idno></series></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0931-7597</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Alkaloid</term><term>Alkylation</term><term>Antitumor</term><term>Antitumor agents</term><term>Aryl isonitriles</term><term>Camptothecin</term><term>Cascade</term><term>Chem</term><term>Curran</term><term>Cyclization</term><term>Dihydroxylation</term><term>Heck cyclization</term><term>Hexacyclic</term><term>Hexacyclic analogues</term><term>Iododesilylation</term><term>Isonitrile</term><term>Isonitriles</term><term>Josien</term><term>Lactol</term><term>Lactol oxidation</term><term>Lactone</term><term>Metalation</term><term>Metalation reactions</term><term>Multi</term><term>Multi substituents</term><term>Other penta</term><term>Penta</term><term>Propargylating</term><term>Propargylating agent</term><term>Pyridone</term><term>Reaction camptothecin</term><term>Regiocontrolled</term><term>Regiocontrolled cascade</term><term>Sharpless</term><term>Substituents</term><term>Title alkaloid</term><term>Univ</term></keywords><keywords scheme="Teeft" xml:lang="en"><term>Alkaloid</term><term>Alkylation</term><term>Antitumor</term><term>Antitumor agents</term><term>Aryl isonitriles</term><term>Camptothecin</term><term>Cascade</term><term>Chem</term><term>Curran</term><term>Cyclization</term><term>Dihydroxylation</term><term>Heck cyclization</term><term>Hexacyclic</term><term>Hexacyclic analogues</term><term>Iododesilylation</term><term>Isonitrile</term><term>Isonitriles</term><term>Josien</term><term>Lactol</term><term>Lactol oxidation</term><term>Lactone</term><term>Metalation</term><term>Metalation reactions</term><term>Multi</term><term>Multi substituents</term><term>Other penta</term><term>Penta</term><term>Propargylating</term><term>Propargylating agent</term><term>Pyridone</term><term>Reaction camptothecin</term><term>Regiocontrolled</term><term>Regiocontrolled cascade</term><term>Sharpless</term><term>Substituents</term><term>Title alkaloid</term><term>Univ</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.</div></front></TEI><affiliations><list><country><li>États-Unis</li></country><region><li>Pennsylvanie</li></region></list><tree><country name="États-Unis"><region name="Pennsylvanie"><name sortKey="Josien, H" sort="Josien, H" uniqKey="Josien H" first="H." last="Josien">H. Josien</name></region><name sortKey="Bom, D" sort="Bom, D" uniqKey="Bom D" first="D." last="Bom">D. Bom</name><name sortKey="Curran, D P" sort="Curran, D P" uniqKey="Curran D" first="D. P." last="Curran">D. P. Curran</name><name sortKey="Ko, S" sort="Ko, S" uniqKey="Ko S" first="S." last="Ko">S. Ko</name></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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