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Cross and ring-closing metathesis of 1,3-diynes: metallotropic [1,3]-shift of ruthenium carbenes.
J Am Chem Soc. 2005 Sep 21; 127(37):12818-9.JA

Abstract

The regio- and stereoselective enyne CM and RCM reactions involving 1,3-diynes have been developed. The ring-closing metathesis of enediynes induces a facile metallotropic [1,3]-shift of alkynyl ruthenium carbene species, thereby providing a unique entry into the synthesis of fully conjugated 1,5-diene-3-ynes.

Authors+Show Affiliations

Department of Chemistry, University of Wisconsin, Madison, Wisconsin 53706, USA.No affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article
Research Support, N.I.H., Extramural
Research Support, U.S. Gov't, Non-P.H.S.
Research Support, U.S. Gov't, P.H.S.

Language

eng

PubMed ID

16159273

Citation

Kim, Mansuk, et al. "Cross and Ring-closing Metathesis of 1,3-diynes: Metallotropic [1,3]-shift of Ruthenium Carbenes." Journal of the American Chemical Society, vol. 127, no. 37, 2005, pp. 12818-9.
Kim M, Miller RL, Lee D. Cross and ring-closing metathesis of 1,3-diynes: metallotropic [1,3]-shift of ruthenium carbenes. J Am Chem Soc. 2005;127(37):12818-9.
Kim, M., Miller, R. L., & Lee, D. (2005). Cross and ring-closing metathesis of 1,3-diynes: metallotropic [1,3]-shift of ruthenium carbenes. Journal of the American Chemical Society, 127(37), 12818-9.
Kim M, Miller RL, Lee D. Cross and Ring-closing Metathesis of 1,3-diynes: Metallotropic [1,3]-shift of Ruthenium Carbenes. J Am Chem Soc. 2005 Sep 21;127(37):12818-9. PubMed PMID: 16159273.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Cross and ring-closing metathesis of 1,3-diynes: metallotropic [1,3]-shift of ruthenium carbenes. AU - Kim,Mansuk, AU - Miller,Reagan L, AU - Lee,Daesung, PY - 2005/9/15/pubmed PY - 2005/12/13/medline PY - 2005/9/15/entrez SP - 12818 EP - 9 JF - Journal of the American Chemical Society JO - J Am Chem Soc VL - 127 IS - 37 N2 - The regio- and stereoselective enyne CM and RCM reactions involving 1,3-diynes have been developed. The ring-closing metathesis of enediynes induces a facile metallotropic [1,3]-shift of alkynyl ruthenium carbene species, thereby providing a unique entry into the synthesis of fully conjugated 1,5-diene-3-ynes. SN - 0002-7863 UR - https://www.unboundmedicine.com/medline/citation/16159273/Cross_and_ring_closing_metathesis_of_13_diynes:_metallotropic_[13]_shift_of_ruthenium_carbenes_ DB - PRIME DP - Unbound Medicine ER -