Highly Stereoselective One-Pot Procedure to Prepare Unsymmetrical Bis- and Tris-chalcogenide Alkenes via Addition of Chalcogens to Alkynes
- 13 July 2007
- journal article
- research article
- Published by American Chemical Society (ACS) in Organometallics
- Vol. 26 (17), 4252-4256
- https://doi.org/10.1021/om070229o
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- Organoselenium and Organotellurium Compounds: Toxicology and PharmacologyChemical Reviews, 2004
- Hydroselenation of Alkynes by Lithium Butylselenolate: An Approach in the Synthesis of Vinylic SelenidesOrganic Letters, 2004
- Stereoselective preparation of conjugated E-enynes from E-vinylic tellurides and terminal alkynes via Sonogashira cross-couplingElectronic supplementary information (ESI) available: spectroscopic data for all new compounds as well as detailed experimental procedures. See http://www.rsc.org/suppdata/ob/b4/b401059k/Organic & Biomolecular Chemistry, 2004
- Palladium-Catalyzed Coupling of sp2-Hybridized TelluridesAccounts of Chemical Research, 2003
- Chalcogen electrophile induced rearrangement of 1-alkynyltrialkyl borates: controlled syntheses of trisubstituted olefins from 1-alkynesTetrahedron, 2001
- Synthesis of (Z)-1-phenylseleno-1,4-diorganyl-1-buten-3-ynes: hydroselenation of symmetrical and unsymmetrical 1,4-diorganyl-1,3-butadiynesTetrahedron, 2001
- Synthesis of Polyacetylenic Acids Isolated from Heisteria acuminataOrganic Letters, 2001
- Synthesis of ketene phenyltelluroacetals by a Wittig-Horner routeTetrahedron Letters, 1995
- Vinylic selenidesJournal of Organometallic Chemistry, 1983
- Silicon-containing carbonyl equivalentsChemical Society Reviews, 1982