[PDF][PDF] Enantioselective synthesis of 2, 4, 5-trisubstituted tetrahydropyrans via peptide-catalyzed Michael addition followed by Kishi's reductive cyclization
A Ueda, M Higuchi, T Umeno, M Tanaka - Heterocycles, 2018 - nagasaki-u.repo.nii.ac.jp
An enantioselective synthesis of 2, 4, 5-trisubstituted tetrahydropyrans has been achieved in
four steps from α, β-unsaturated ketones and dimethyl malonate by peptide-catalyzed …
four steps from α, β-unsaturated ketones and dimethyl malonate by peptide-catalyzed …
Enantioselective Synthesis of 2, 4, 5-Trisubstituted Tetrahydropyrans via Peptide-Catalyzed Michael Addition Followed by Kishi's Reductive Cyclization
A Ueda, M Higuchi, T Umeno, M Tanaka - HETEROCYCLES, 2018 - cir.nii.ac.jp
抄録 An enantioselective synthesis of 2, 4, 5-trisubstituted tetrahydropyrans has been
achieved in four steps from α, β-unsaturated ketones and dimethyl malonate by peptide …
achieved in four steps from α, β-unsaturated ketones and dimethyl malonate by peptide …
[PDF][PDF] ENANTIOSELECTIVE SYNTHESIS OF 2, 4, 5-TRISUBSTITUTED TETRAHYDROPYRANS VIA PEPTIDE-CATALYZED MICHAEL ADDITION FOLLOWED BY …
A Ueda, M Higuchi, T Umeno, M Tanaka - scholar.archive.org
An enantioselective synthesis of 2, 4, 5-trisubstituted tetrahydropyrans has been achieved in
four steps from α, β-unsaturated ketones and dimethyl malonate by peptide-catalyzed …
four steps from α, β-unsaturated ketones and dimethyl malonate by peptide-catalyzed …
Enantioselective Synthesis of 2, 4, 5-Trisubstituted Tetrahydropyrans via Peptide-Catalyzed Michael Addition Followed by Kishi's Reductive Cyclization
A Ueda, M Higuchi, T Umeno… - HETEROCYCLES, 2018 - nagasaki-u.repo.nii.ac.jp
An enantioselective synthesis of 2, 4, 5-trisubstituted tetrahydropyrans has been achieved in
four steps from α, β-unsaturated ketones and dimethyl malonate by peptide-catalyzed …
four steps from α, β-unsaturated ketones and dimethyl malonate by peptide-catalyzed …
[PDF][PDF] ENANTIOSELECTIVE SYNTHESIS OF 2, 4, 5-TRISUBSTITUTED TETRAHYDROPYRANS VIA PEPTIDE-CATALYZED MICHAEL ADDITION FOLLOWED BY …
A Ueda, M Higuchi, T Umeno… - …, 2019 - pdfs.semanticscholar.org
An enantioselective synthesis of 2, 4, 5-trisubstituted tetrahydropyrans has been achieved in
four steps from α, β-unsaturated ketones and dimethyl malonate by peptide-catalyzed …
four steps from α, β-unsaturated ketones and dimethyl malonate by peptide-catalyzed …
[引用][C] ENANTIOSELECTIVE SYNTHESIS OF 2, 4, 5-TRISUBSTITUTED TETRAHYDROPYRANS VIA PEPTIDE-CATALYZED MICHAEL ADDITION FOLLOWED BY …
A UEDA, M HIGUCHI, T UMENO, M TANAKA - Heterocycles, 2019 - jglobal.jst.go.jp
ENANTIOSELECTIVE SYNTHESIS OF 2,4,5-TRISUBSTITUTED TETRAHYDROPYRANS
VIA PEPTIDE-CATALYZED MICHAEL ADDITION FOLLOWED BY KISHI’S REDUCTIVE …
VIA PEPTIDE-CATALYZED MICHAEL ADDITION FOLLOWED BY KISHI’S REDUCTIVE …
[引用][C] ENANTIOSELECTIVE SYNTHESIS OF 2, 4, 5-TRISUBSTITUTED TETRAHYDROPYRANS VIA PEPTIDE-CATALYZED MICHAEL ADDITION FOLLOWED BY …
A Ueda, M Higuchi, T Umeno, M Tanaka - Heterocycles: an international …, 2019 - cir.nii.ac.jp
ENANTIOSELECTIVE SYNTHESIS OF 2,4,5-TRISUBSTITUTED TETRAHYDROPYRANS VIA
PEPTIDE-CATALYZED MICHAEL ADDITION FOLLOWED BY KISHI'S REDUCTIVE …
PEPTIDE-CATALYZED MICHAEL ADDITION FOLLOWED BY KISHI'S REDUCTIVE …