Improved Protocol for Asymmetric, Intramolecular Heteroatom Michael Addition Using Organocatalysis: Enantioselective Syntheses of Homoproline, Pelletierine, and Homopipecolic Acid-Reference-Cited by-同舟云学术

Improved Protocol for Asymmetric, Intramolecular Heteroatom Michael Addition Using Organocatalysis: Enantioselective Syntheses of Homoproline, Pelletierine, and Homopipecolic Acid

Published:2008-06-05 Issue:13 Volume:73 Page:5155-5158
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Carlson Erik C.¹,Rathbone Lauren K.¹,Yang Hua¹,Collett Nathan D.¹,Carter Rich G.¹

Affiliation:

1. Department of Chemistry, 153 Gilbert Hall, Oregon State University, Corvallis, Oregon 97331

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo800749t

Reference67 articles.

1. Regioselective, Diastereoselective, and Enantioselective Lithiation−Substitution Sequences: Reaction Pathways and Synthetic Applications

2. Enantioselective Synthesis with Lithium/(−)-Sparteine Carbanion Pairs

3. Beyond Thermodynamic Acidity: A Perspective on the Complex-Induced Proximity Effect (CIPE) in Deprotonation Reactions

4. Reactivity series for s-BuLi/diamine-mediated lithiation of N-Boc pyrrolidine: applications in catalysis and lithiation of N-Boc piperidine

5. Enantioselectivity in the Reactions of Chiral α-(N-Carbamoyl)alkylcuprates

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