Solvent-controlled addition of alkynyltins or allylic tins to aldehydes catalyzed by indium trichloride
- 25 December 1995
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 36 (52) , 9497-9500
- https://doi.org/10.1016/0040-4039(95)02057-8
Abstract
No abstract availableKeywords
Funding Information
- Ministry of Education, Culture, Sports, Science and Technology
This publication has 25 references indexed in Scilit:
- Synthesis of anti-Homoallylic Alcohols and Monoprotected 1,2-Diols through InCl3-Promoted Addition of Allylic Stannanes to AldehydesThe Journal of Organic Chemistry, 1995
- Palladium- and platinum-catalysed addition of aldehydes with allylstannanesJournal of the Chemical Society, Chemical Communications, 1995
- Synthesis of .alpha.,.alpha.,.beta.,.beta.-Tetrasubstituted .beta.-Lactones from Ketones, Ethyl .alpha.-Bromoisobutyrate, and Indium or Zinc. Factors Influencing the .beta.-Lactone Formation in the Electrochemical and the Classical Procedure of the Reformatsky ReactionThe Journal of Organic Chemistry, 1994
- New triad alkylation reagent. Cross coupling of indium trialkyls with alkenyl halidesJournal of the American Chemical Society, 1992
- The synthesis of cembranolide precursors via addition of allylstannanes to conjugated aldehydesThe Journal of Organic Chemistry, 1986
- Remote chirality control in 1,2-asymmetric induction: a remarkable difference between the meso- and (±)-isomers of dimethylglutaric hemialdehydeJournal of the Chemical Society, Chemical Communications, 1985
- Organotin chemistry for synthesis applicationsPublished by Walter de Gruyter GmbH ,1981
- Mild, selective, general method of ketone synthesis from acid chlorides and organotin compounds catalyzed by palladiumThe Journal of Organic Chemistry, 1979
- ALKYLATION, ARYLATION, AND VINYLATION OF ACYL CHLORIDES BY MEANS OF ORGANOTIN COMPOUNDS IN THE PRESENCE OF CATALYTIC AMOUNTS OF TETRAKIS(TRIPHENYLPHOSPHINE)PALLADIUM(O)Chemistry Letters, 1977
- Triphenylindium1Journal of the American Chemical Society, 1940