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- Publisher Website: 10.1021/np980418z
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Article: Stereoselective total synthesis of (3R,8S)-falcarindiol, a common polyacetylenic compound from umbellifers
Title | Stereoselective total synthesis of (3R,8S)-falcarindiol, a common polyacetylenic compound from umbellifers |
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Authors | |
Issue Date | 1999 |
Publisher | American 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? |
Abstract | The 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 Identifier | http://hdl.handle.net/10722/167614 |
ISSN | 2023 Impact Factor: 3.3 2023 SCImago Journal Rankings: 0.802 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Zheng, G | en_US |
dc.contributor.author | Lu, W | en_US |
dc.contributor.author | Cai, J | en_US |
dc.date.accessioned | 2012-10-08T03:09:05Z | - |
dc.date.available | 2012-10-08T03:09:05Z | - |
dc.date.issued | 1999 | en_US |
dc.identifier.citation | Journal Of Natural Products, 1999, v. 62 n. 4, p. 626-628 | en_US |
dc.identifier.issn | 0163-3864 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/167614 | - |
dc.description.abstract | The 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.language | eng | en_US |
dc.publisher | American Chemical Society. The Journal's web site is located at http://pubs.acs.org/jnp | en_US |
dc.relation.ispartof | Journal of Natural Products | en_US |
dc.title | Stereoselective total synthesis of (3R,8S)-falcarindiol, a common polyacetylenic compound from umbellifers | en_US |
dc.type | Article | en_US |
dc.identifier.email | Lu, W:luwei@hku.hk | en_US |
dc.identifier.authority | Lu, W=rp00754 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1021/np980418z | en_US |
dc.identifier.scopus | eid_2-s2.0-0032901889 | en_US |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-0032901889&selection=ref&src=s&origin=recordpage | en_US |
dc.identifier.volume | 62 | en_US |
dc.identifier.issue | 4 | en_US |
dc.identifier.spage | 626 | en_US |
dc.identifier.epage | 628 | en_US |
dc.identifier.isi | WOS:000079959300023 | - |
dc.publisher.place | United States | en_US |
dc.identifier.scopusauthorid | Zheng, G=55112184700 | en_US |
dc.identifier.scopusauthorid | Lu, W=27868087600 | en_US |
dc.identifier.scopusauthorid | Cai, J=26643616800 | en_US |
dc.identifier.issnl | 0163-3864 | - |