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- Publisher Website: 10.1002/anie.200602056
- Scopus: eid_2-s2.0-33749006267
- PMID: 16906616
- WOS: WOS:000240815100028
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Article: Total synthesis of pseudolaric acid A
Title | Total synthesis of pseudolaric acid A |
---|---|
Authors | |
Keywords | Antitumor agents Carbenoids Domino reactions Natural products Total synthesis |
Issue Date | 2006 |
Publisher | Wiley - V C H Verlag GmbH & Co. KGaA. The Journal's web site is located at http://www3.interscience.wiley.com/journal/26737/home |
Citation | Angewandte Chemie - International Edition, 2006, v. 45 n. 37, p. 6197-6201 How to Cite? |
Abstract | (Chemical Equation Presented) The antiangiogenic and cytotoxic natural product pseudolaric acid A ((-)-1) has been obtained by a 26-step synthetic route. This enantioselective synthesis employed an intramolecular carbene cyclization cycloaddition cascade reaction as the key step to construct the carbocyclic framework. PMB = para-methoxybenzyl. © 2006 Wiley-VCH Verlag GmbH & Co. KGaA. |
Persistent Identifier | http://hdl.handle.net/10722/70285 |
ISSN | 2023 Impact Factor: 16.1 2023 SCImago Journal Rankings: 5.300 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Geng, Z | en_HK |
dc.contributor.author | Chen, B | en_HK |
dc.contributor.author | Chiu, P | en_HK |
dc.date.accessioned | 2010-09-06T06:21:26Z | - |
dc.date.available | 2010-09-06T06:21:26Z | - |
dc.date.issued | 2006 | en_HK |
dc.identifier.citation | Angewandte Chemie - International Edition, 2006, v. 45 n. 37, p. 6197-6201 | en_HK |
dc.identifier.issn | 1433-7851 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/70285 | - |
dc.description.abstract | (Chemical Equation Presented) The antiangiogenic and cytotoxic natural product pseudolaric acid A ((-)-1) has been obtained by a 26-step synthetic route. This enantioselective synthesis employed an intramolecular carbene cyclization cycloaddition cascade reaction as the key step to construct the carbocyclic framework. PMB = para-methoxybenzyl. © 2006 Wiley-VCH Verlag GmbH & Co. KGaA. | en_HK |
dc.language | eng | en_HK |
dc.publisher | Wiley - V C H Verlag GmbH & Co. KGaA. The Journal's web site is located at http://www3.interscience.wiley.com/journal/26737/home | en_HK |
dc.relation.ispartof | Angewandte Chemie - International Edition | en_HK |
dc.subject | Antitumor agents | en_HK |
dc.subject | Carbenoids | en_HK |
dc.subject | Domino reactions | en_HK |
dc.subject | Natural products | en_HK |
dc.subject | Total synthesis | en_HK |
dc.title | Total synthesis of pseudolaric acid A | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=1433-7851&volume=45&spage=6197&epage=6201&date=2006&atitle=Total+synthesis+of+pseudolaric+acid+A+ | en_HK |
dc.identifier.email | Chiu, P:pchiu@hku.hk | en_HK |
dc.identifier.authority | Chiu, P=rp00680 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1002/anie.200602056 | en_HK |
dc.identifier.pmid | 16906616 | - |
dc.identifier.scopus | eid_2-s2.0-33749006267 | en_HK |
dc.identifier.hkuros | 124481 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-33749006267&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 45 | en_HK |
dc.identifier.issue | 37 | en_HK |
dc.identifier.spage | 6197 | en_HK |
dc.identifier.epage | 6201 | en_HK |
dc.identifier.eissn | 1521-3773 | - |
dc.identifier.isi | WOS:000240815100028 | - |
dc.publisher.place | Germany | en_HK |
dc.identifier.scopusauthorid | Geng, Z=36947090200 | en_HK |
dc.identifier.scopusauthorid | Chen, B=37160914300 | en_HK |
dc.identifier.scopusauthorid | Chiu, P=11140148700 | en_HK |
dc.identifier.issnl | 1433-7851 | - |