Tributyl[2-(trimethylsilyl)-prop-2-enyl]stannane: A Highly Efficient Reagent for the Allylation of Radicals

Article Properties
  • Publication Date
    1994/09/28
  • Journal
  • Indian UGC (journal)
  • Citations
    7
  • Philippe Renaud
  • Michèle Gerster
  • Marco Ribezzo
Abstract
Cite
Renaud, Philippe, et al. “Tributyl[2-(trimethylsilyl)-Prop-2-enyl]stannane: A Highly Efficient Reagent for the Allylation of Radicals”. CHIMIA, vol. 48, no. 9, 1994, p. 366, https://doi.org/10.2533/chimia.1994.366.
Renaud, P., Gerster, M., & Ribezzo, M. (1994). Tributyl[2-(trimethylsilyl)-prop-2-enyl]stannane: A Highly Efficient Reagent for the Allylation of Radicals. CHIMIA, 48(9), 366. https://doi.org/10.2533/chimia.1994.366
Renaud, Philippe, Michèle Gerster, and Marco Ribezzo. “Tributyl[2-(trimethylsilyl)-Prop-2-enyl]stannane: A Highly Efficient Reagent for the Allylation of Radicals”. CHIMIA 48, no. 9 (1994): 366. https://doi.org/10.2533/chimia.1994.366.
Renaud P, Gerster M, Ribezzo M. Tributyl[2-(trimethylsilyl)-prop-2-enyl]stannane: A Highly Efficient Reagent for the Allylation of Radicals. CHIMIA. 1994;48(9):366.
Citations
Title Journal Journal Categories Citations Publication Date
Ozone Oxidation of Silylalkene: Mechanistic Study and Application for the Synthesis of Silacarboxylic Acid Derivatives The Journal of Organic Chemistry
  • Science: Chemistry: Organic chemistry
  • Science: Chemistry: Analytical chemistry
  • Technology: Chemical technology: Polymers and polymer manufacture
  • Science: Chemistry
7 2020
α-Allylation of α-amino acids via 1,5-hydrogen atom transfer Tetrahedron Letters
  • Science: Chemistry: Organic chemistry
  • Science: Chemistry: Analytical chemistry
  • Technology: Chemical technology: Polymers and polymer manufacture
  • Science: Chemistry
9 2009
Stereoselective Reactions of Phthalimido‐Substituted Radicals Derived from (±)‐Threonine: A comparison with reactions of N‐phthaloyliminium ions

Helvetica Chimica Acta
  • Science: Chemistry: General. Including alchemy
  • Science: Chemistry: Analytical chemistry
  • Science: Chemistry
9 1998
Radical Allylations with Trimethyl[2- [(tributylstannyl)methyl]-2-propenyl]silane or Trimethyl[2-[(triphenylstannyl)- methyl]-2-propenyl]silane The Journal of Organic Chemistry
  • Science: Chemistry: Organic chemistry
  • Science: Chemistry: Analytical chemistry
  • Technology: Chemical technology: Polymers and polymer manufacture
  • Science: Chemistry
25 1997
Synthesis of 2-functionalized allyl tris(trimethylsilyl)silanes Tetrahedron Letters
  • Science: Chemistry: Organic chemistry
  • Science: Chemistry: Analytical chemistry
  • Technology: Chemical technology: Polymers and polymer manufacture
  • Science: Chemistry
21 1996
Citations Analysis
The category Science: Chemistry: Analytical chemistry 6 is the most commonly referenced area in studies that cite this article. The first research to cite this article was titled Radical allylation of α-silylacetic esters and was published in 1995. The most recent citation comes from a 2020 study titled Ozone Oxidation of Silylalkene: Mechanistic Study and Application for the Synthesis of Silacarboxylic Acid Derivatives. This article reached its peak citation in 1995, with 2 citations. It has been cited in 5 different journals. Among related journals, the The Journal of Organic Chemistry cited this research the most, with 2 citations. The chart below illustrates the annual citation trends for this article.
Citations used this article by year