ϟ
DOI: 10.1002/chin.201133204
OpenAccess: Closed
This work is not Open Acccess. We may still have a PDF, if this is the case there will be a green box below.
ChemInform Abstract: Highly Enantioselective Synthesis of Designed Chiral Acyclonucleosides and Acyclonucleotides by Organocatalytic Aza‐Michael Addition.
Hai‐Ming Guo,Teng‐Fei Yuan,Hong‐Ying Niu,Jin‐Ying Liu,Runze Mao,Deyang Li,Gui‐Rong Qu
Chemistry
Enantioselective synthesis
Michael reaction
2011
Abstract Organocatalytic aza‐Michael addition of purine bases (I) towards enals (II) is successfully applied for the first time to give acyclonucleosides (III) in high yields and good to excellent enantioselectivities.
Loading...
- MLA
- APA
- Chicago
- IEEE
- Harvard
- BibTeX
Cite this:
Generate Citation
“ChemInform Abstract: Highly Enantioselective Synthesis of Designed Chiral Acyclonucleosides and Acyclonucleotides by Organocatalytic Aza‐Michael Addition.” is a paper by Hai‐Ming Guo Teng‐Fei Yuan Hong‐Ying Niu Jin‐Ying Liu Runze Mao Deyang Li Gui‐Rong Qu published in 2011. It has an Open Access status of “closed”. You can read and download a PDF Full Text of this paper here.