Stereoselective peterson olefinations of silylated benzyl carbamates

Article Properties
  • Language
    English
  • DOI (url)
    10.1016/s0040-4020(98)00070-2
  • Publication Date
    1998/03/01
  • Journal
    Tetrahedron
  • Indian UGC (journal)
  • Refrences
    42
  • L. Frances van Staden
  • Birgit Bartels-Rahm
  • John S. Field
  • Neville D. Emslie
Cite
Frances van Staden, L., et al. “Stereoselective Peterson Olefinations of Silylated Benzyl Carbamates”. Tetrahedron, vol. 54, no. 13, 1998, pp. 3255-78, https://doi.org/10.1016/s0040-4020(98)00070-2.
Frances van Staden, L., Bartels-Rahm, B., Field, J. S., & Emslie, N. D. (1998). Stereoselective peterson olefinations of silylated benzyl carbamates. Tetrahedron, 54(13), 3255-3278. https://doi.org/10.1016/s0040-4020(98)00070-2
Frances van Staden, L., Birgit Bartels-Rahm, John S. Field, and Neville D. Emslie. “Stereoselective Peterson Olefinations of Silylated Benzyl Carbamates”. Tetrahedron 54, no. 13 (1998): 3255-78. https://doi.org/10.1016/s0040-4020(98)00070-2.
Frances van Staden L, Bartels-Rahm B, Field JS, Emslie ND. Stereoselective peterson olefinations of silylated benzyl carbamates. Tetrahedron. 1998;54(13):3255-78.
Journal Categories
Science
Chemistry
Science
Chemistry
Analytical chemistry
Science
Chemistry
Organic chemistry
Technology
Chemical technology
Polymers and polymer manufacture
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Refrences
Title Journal Journal Categories Citations Publication Date
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 1997
A new route to α-fluorovinylphosphonates utilizing Peterson olefination methodology Tetrahedron
  • Science: Chemistry: Organic chemistry
  • Science: Chemistry: Analytical chemistry
  • Technology: Chemical technology: Polymers and polymer manufacture
  • Science: Chemistry
 31 1996
Structure--Stability Relationships in Unsaturated Sulfur Compounds. VIII. Thermodynamics of the Geometric Isomers of Vinyl Sulfides, Sulfoxides and Sulfones. Acta Chemica Scandinavica 1 1996
Efficient preparation of trisubstituted alkenes using the Julia-Lythgoe olefination of ketones. On the key-role of SmI2 in the reductive elimination step Tetrahedron Letters
  • Science: Chemistry: Organic chemistry
  • Science: Chemistry: Analytical chemistry
  • Technology: Chemical technology: Polymers and polymer manufacture
  • Science: Chemistry
 35 1996
10.1016/S0040-4020(01)90461-2 Tetrahedron
  • Science: Chemistry: Organic chemistry
  • Science: Chemistry: Analytical chemistry
  • Technology: Chemical technology: Polymers and polymer manufacture
  • Science: Chemistry
 1994
Refrences Analysis
Category Category Repetition
Science: Chemistry18
Science: Chemistry: Analytical chemistry14
Science: Chemistry: Organic chemistry12
Technology: Chemical technology: Polymers and polymer manufacture12
Science: Chemistry: General. Including alchemy6
The category Science: Chemistry 18 is the most frequently represented among the references in this article. It primarily includes studies from Tetrahedron Letters The chart below illustrates the number of referenced publications per year.
Refrences used by this article by year