WebIngrid Apeland is an academic researcher from University of Bergen. The author has contributed to research in topic(s): Furanose & Dithiol. The author has an hindex of 1, co-authored 2 publication(s) receiving 10 citation(s). Web9 sep. 2024 · The enantioselective [1,2]-carbonyl addition of a lithium acetylide was first disclosed by Mukaiyama 12 and later improved by the Merck 13 group in the synthesis of the HIV-1 reverse transcriptase inhibitor efavirenz. However, these early examples required several equivalents of ligand to impart high enantioselectivity.
The Preparation of Lithium Acetylide-Ethylenediamine
WebStereospecifically deuteriated samples of D-propargylglycine 1 have been prepared by reaction of the labelled Pmc-protected aziridine free acids 22 with a lithium acetylide followed by deprotection.These samples have been used to show that D-amino acid oxidase, in converting D-propargylglycine to the lactone 5, deprotonates C-3 in a non … Web26 aug. 2024 · Acidity of Terminal Alkynes: Formation of Acetylide Anions. Terminal alkynes are much more acidic than most other hydrocarbons. Removal of the proton leads to the formation of an acetylide anion, RC=C:-.The origin of the enhanced acidity can be attributed to the stability of the acetylide anion, which has the unpaired electrons in an … small dogs that bite
Lithium carbide C2Li2 ChemSpider
Web3 apr. 1995 · Pergamon 0040-4039(95)00279-0 Tetrahedron Letters, Vol. 36, No, 14, pp. 2369-2372, 1995 Elsevier Science Ltd Printed in Great Britain 0040-4039/95 $9.50+0.00 ACETYLIDE ANIONS EXERT COMPLETE CONTROL OVER ALDOLIZATION DURING THE DIRECT CONVERSION OF SOUARATE ESTERS INTO POLYQUINANES Tina … Webof the unsaturated sulfonamide 2 to a lithium acetylide ( e.g. 3) leads to three products; what appears to be the 1,4-addition product 4,diyne5 and enediyne 6 (Scheme 3). Furthermore, increasing the temperature of the reaction improves the yield of the diyne and enediyne. Interestingly, both 4 and 6 were iso-lated as single geometrical isomers. Web15 apr. 2001 · The resulting mixture is boiled under reflux for 12 h to ensure disproportionation of any Lithium Acetylide. From Trichloroethylene : 3 to 100 mL of 1∶1 mixture of anhydrous ether and THF is added 0.6 mol BuLi, cooled to −78 °C, and 0.2 mol Trichloroethylene in 50 mL of ether is added dropwise over 20 min. small dogs that don\u0027t shed much