P(CH3NCH2CH2)3N as a Dehydrobromination Reagent: Synthesis of Vitamin A Derivatives Revisited
Author:
Affiliation:
1. Department of Chemistry, Iowa State University, Ames, Iowa 50011-3111
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo010648%2B
Reference42 articles.
1. New Prophosphatranes: Novel intermediates to five-coordinate phosphatranes
2. Atranes: new examples with unexpected properties
3. pKa Measurements of P(RNCH2CH3)3N
4. P(CH3NCH2CH2)3N: A Nonionic Superbase for Efficient Dehydrohalogenation
5. Free and Polymer-Bound Tricyclic Azaphosphatranes HP(RNCH2CH2)3N+: Procatalysts in Dehydrohalogenations and Debrominations with NaH
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2. Fragmentation and skeletal rearrangements of products of the reaction between fluorobenzenes and bicyclic N-bases studied by electron ionization mass spectrometry;International Journal of Mass Spectrometry;2005-01
3. One or More CC Bond(s) by Elimination of Hydrogen, Carbon, Halogen, or Oxygen Functions;Comprehensive Organic Functional Group Transformations II;2005
4. Highly efficient phosphine-catalyzed aza-Michael reactions of α,β-unsaturated compounds with carbamates in the presence of TMSCl;Tetrahedron Letters;2004-05
5. Proazaphosphatranes [P(RNCH2CH2)3N,R= Me,i-Pr,i-Bu];Encyclopedia of Reagents for Organic Synthesis;2004-04-15
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