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A three-component tandem reductive aldol reaction catalyzed by N-heterocyclic carbene-copper complexes

(2006) ORGANIC LETTERS. 8(26). p.6059-6062
Author
Organization
Abstract
An efficient catalytic system for the three-component coupling of electrophilic alkenes, aldehydes, and silane was optimized with a new family of copper N-heterocyclic carbene complexes. These catalysts do not require activation and show high activity (TOF > 15 000 h(-1)) as well as some anti diastereoselectivity.
Keywords
CONJUGATE ADDITION, ENANTIOSELECTIVE SYNTHESIS, CARBONYL-COMPOUNDS, ASYMMETRIC-SYNTHESIS, GRIGNARD-REAGENTS, STRYKERS REAGENT, CYCLIZATION, KETONES, NHC, HYDROSILYLATION

Citation

Please use this url to cite or link to this publication:

MLA
Welle, Alexandre, et al. “A Three-Component Tandem Reductive Aldol Reaction Catalyzed by N-Heterocyclic Carbene-Copper Complexes.” ORGANIC LETTERS, vol. 8, no. 26, 2006, pp. 6059–62.
APA
Welle, A., Diez-Gonzalez, S., Tinant, B., Nolan, S., & Riant, O. (2006). A three-component tandem reductive aldol reaction catalyzed by N-heterocyclic carbene-copper complexes. ORGANIC LETTERS, 8(26), 6059–6062.
Chicago author-date
Welle, Alexandre, Silvia Diez-Gonzalez, Bernard Tinant, Steven Nolan, and Olivier Riant. 2006. “A Three-Component Tandem Reductive Aldol Reaction Catalyzed by N-Heterocyclic Carbene-Copper Complexes.” ORGANIC LETTERS 8 (26): 6059–62.
Chicago author-date (all authors)
Welle, Alexandre, Silvia Diez-Gonzalez, Bernard Tinant, Steven Nolan, and Olivier Riant. 2006. “A Three-Component Tandem Reductive Aldol Reaction Catalyzed by N-Heterocyclic Carbene-Copper Complexes.” ORGANIC LETTERS 8 (26): 6059–6062.
Vancouver
1.
Welle A, Diez-Gonzalez S, Tinant B, Nolan S, Riant O. A three-component tandem reductive aldol reaction catalyzed by N-heterocyclic carbene-copper complexes. ORGANIC LETTERS. 2006;8(26):6059–62.
IEEE
[1]
A. Welle, S. Diez-Gonzalez, B. Tinant, S. Nolan, and O. Riant, “A three-component tandem reductive aldol reaction catalyzed by N-heterocyclic carbene-copper complexes,” ORGANIC LETTERS, vol. 8, no. 26, pp. 6059–6062, 2006.
@article{8169876,
  abstract     = {An efficient catalytic system for the three-component coupling of electrophilic alkenes, aldehydes, and silane was optimized with a new family of copper N-heterocyclic carbene complexes. These catalysts do not require activation and show high activity (TOF > 15 000 h(-1)) as well as some anti diastereoselectivity.},
  author       = {Welle, Alexandre and Diez-Gonzalez, Silvia and Tinant, Bernard and Nolan, Steven and Riant, Olivier},
  issn         = {1523-7060},
  journal      = {ORGANIC LETTERS},
  keywords     = {CONJUGATE ADDITION,ENANTIOSELECTIVE SYNTHESIS,CARBONYL-COMPOUNDS,ASYMMETRIC-SYNTHESIS,GRIGNARD-REAGENTS,STRYKERS REAGENT,CYCLIZATION,KETONES,NHC,HYDROSILYLATION},
  language     = {eng},
  number       = {26},
  pages        = {6059--6062},
  title        = {A three-component tandem reductive aldol reaction catalyzed by N-heterocyclic carbene-copper complexes},
  url          = {http://dx.doi.org/10.1021/ol062495o},
  volume       = {8},
  year         = {2006},
}

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