reference/1069276

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/1069276

Outgoing Links

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contentType	Journal Article\|Research Support, N.I.H., Extramural\|Research Support, U.S. Gov't, Non-P.H.S.
endingPage	5368
issn	1433-7851 1521-3773
issueIdentifier	29
pageRange	5366-5368
publicationName	Angewandte Chemie (International ed. in English)
startingPage	5366
hasFundingAgency	http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_5a0eb2fadabf1dffb4d70280b760adba http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_a1ebfe17b0713ecaf89801f0370c078d
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bibliographicCitation	Trenkle JD, Jamison TF. Macrocyclization by nickel-catalyzed, ester-promoted, epoxide-alkyne reductive coupling: total synthesis of (-)-gloeosporone. Angew Chem Int Ed Engl. 2009;48(29):5366–8. PMID: 19536804; PMCID: PMC2806845.
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date	200907
identifier	https://doi.org/10.1002/anie.200902079 https://pubmed.ncbi.nlm.nih.gov/PMC2806845 https://pubmed.ncbi.nlm.nih.gov/19536804
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Macrocyclization by Nickel‐Catalyzed, Ester‐Promoted, Epoxide–Alkyne Reductive Coupling: Total Synthesis of (−)‐Gloeosporone
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Total number of triples: 57.