File Download

There are no files associated with this item.

  Links for fulltext
     (May Require Subscription)
Supplementary

Article: Stereoselective total synthesis of (3R,8S)-falcarindiol, a common polyacetylenic compound from umbellifers

TitleStereoselective total synthesis of (3R,8S)-falcarindiol, a common polyacetylenic compound from umbellifers
Authors
Zheng, GLu, WCai, J
Issue Date1999
PublisherAmerican Chemical Society. The Journal's web site is located at http://pubs.acs.org/jnp
Citation
Journal Of Natural Products, 1999, v. 62 n. 4, p. 626-628 How to Cite?
DOI: http://dx.doi.org/10.1021/np980418z
AbstractThe first stereoselective total synthesis of (3R,8S)-falcarindiol (1) from L-tartaric acid and D-xylose is reported, via the Cadiot-Chodkiczwicz reaction, to couple 1-bromoalkyne (2) with 3(R)-(tert-butyldiphenylsilyloxy)- 1-penten-4-yne (3).
Persistent Identifierhttp://hdl.handle.net/10722/167614
ISSN
0163-3864
2021 Impact Factor: 4.803
2020 SCImago Journal Rankings: 0.976
ISI Accession Number ID
WOS:000079959300023
References
References in Scopus

 

DC FieldValueLanguage
dc.contributor.authorZheng, Gen_US
dc.contributor.authorLu, Wen_US
dc.contributor.authorCai, Jen_US
dc.date.accessioned2012-10-08T03:09:05Z-
dc.date.available2012-10-08T03:09:05Z-
dc.date.issued1999en_US
dc.identifier.citationJournal Of Natural Products, 1999, v. 62 n. 4, p. 626-628en_US
dc.identifier.issn0163-3864en_US
dc.identifier.urihttp://hdl.handle.net/10722/167614-
dc.description.abstractThe first stereoselective total synthesis of (3R,8S)-falcarindiol (1) from L-tartaric acid and D-xylose is reported, via the Cadiot-Chodkiczwicz reaction, to couple 1-bromoalkyne (2) with 3(R)-(tert-butyldiphenylsilyloxy)- 1-penten-4-yne (3).en_US
dc.languageengen_US
dc.publisherAmerican Chemical Society. The Journal's web site is located at http://pubs.acs.org/jnpen_US
dc.relation.ispartofJournal of Natural Productsen_US
dc.titleStereoselective total synthesis of (3R,8S)-falcarindiol, a common polyacetylenic compound from umbellifersen_US
dc.typeArticleen_US
dc.identifier.emailLu, W:luwei@hku.hken_US
dc.identifier.authorityLu, W=rp00754en_US
dc.description.naturelink_to_subscribed_fulltexten_US
dc.identifier.doi10.1021/np980418zen_US
dc.identifier.scopuseid_2-s2.0-0032901889en_US
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-0032901889&selection=ref&src=s&origin=recordpageen_US
dc.identifier.volume62en_US
dc.identifier.issue4en_US
dc.identifier.spage626en_US
dc.identifier.epage628en_US
dc.identifier.isiWOS:000079959300023-
dc.publisher.placeUnited Statesen_US
dc.identifier.scopusauthoridZheng, G=55112184700en_US
dc.identifier.scopusauthoridLu, W=27868087600en_US
dc.identifier.scopusauthoridCai, J=26643616800en_US
dc.identifier.issnl0163-3864-

Export via OAI-PMH Interface in XML Formats

OR

Export to Other Non-XML Formats