Azotides as Modular Peptide-Based Ligands for Asymmetric Lewis Acid Catalysis

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Standard

Azotides as Modular Peptide-Based Ligands for Asymmetric Lewis Acid Catalysis. / Jacobsen, Christian Borch; Nielsen, Daniel Steen; Meldal, Morten; Diness, Frederik.

I: Journal of Organic Chemistry, Bind 84, Nr. 11, 07.06.2019, s. 6940-6945.

Publikation: Bidrag til tidsskriftTidsskriftartikelfagfællebedømt

Harvard

Jacobsen, CB, Nielsen, DS, Meldal, M & Diness, F 2019, 'Azotides as Modular Peptide-Based Ligands for Asymmetric Lewis Acid Catalysis', Journal of Organic Chemistry, bind 84, nr. 11, s. 6940-6945. https://doi.org/10.1021/acs.joc.9b00732

APA

Jacobsen, C. B., Nielsen, D. S., Meldal, M., & Diness, F. (2019). Azotides as Modular Peptide-Based Ligands for Asymmetric Lewis Acid Catalysis. Journal of Organic Chemistry, 84(11), 6940-6945. https://doi.org/10.1021/acs.joc.9b00732

Vancouver

Jacobsen CB, Nielsen DS, Meldal M, Diness F. Azotides as Modular Peptide-Based Ligands for Asymmetric Lewis Acid Catalysis. Journal of Organic Chemistry. 2019 jun. 7;84(11):6940-6945. https://doi.org/10.1021/acs.joc.9b00732

Author

Jacobsen, Christian Borch ; Nielsen, Daniel Steen ; Meldal, Morten ; Diness, Frederik. / Azotides as Modular Peptide-Based Ligands for Asymmetric Lewis Acid Catalysis. I: Journal of Organic Chemistry. 2019 ; Bind 84, Nr. 11. s. 6940-6945.

Bibtex

@article{5cb0d4d0edaa472598a8e356af58b533,
title = "Azotides as Modular Peptide-Based Ligands for Asymmetric Lewis Acid Catalysis",
abstract = "Synthesis of azotides and evaluation of these as ligands for enantioselective Lewis acid catalysis is reported. The ligands were readily prepared from the chiral pool of amino acids and perform well in the cobalt(II)-catalyzed formation of asymmetric hetero Diels-Alder adducts. A rational for the observed enantioselectivity and conversion rate supported by computational calculations is provided.",
author = "Jacobsen, {Christian Borch} and Nielsen, {Daniel Steen} and Morten Meldal and Frederik Diness",
year = "2019",
month = jun,
day = "7",
doi = "10.1021/acs.joc.9b00732",
language = "English",
volume = "84",
pages = "6940--6945",
journal = "Journal of Organic Chemistry",
issn = "0022-3263",
publisher = "American Chemical Society",
number = "11",

}

RIS

TY - JOUR

T1 - Azotides as Modular Peptide-Based Ligands for Asymmetric Lewis Acid Catalysis

AU - Jacobsen, Christian Borch

AU - Nielsen, Daniel Steen

AU - Meldal, Morten

AU - Diness, Frederik

PY - 2019/6/7

Y1 - 2019/6/7

N2 - Synthesis of azotides and evaluation of these as ligands for enantioselective Lewis acid catalysis is reported. The ligands were readily prepared from the chiral pool of amino acids and perform well in the cobalt(II)-catalyzed formation of asymmetric hetero Diels-Alder adducts. A rational for the observed enantioselectivity and conversion rate supported by computational calculations is provided.

AB - Synthesis of azotides and evaluation of these as ligands for enantioselective Lewis acid catalysis is reported. The ligands were readily prepared from the chiral pool of amino acids and perform well in the cobalt(II)-catalyzed formation of asymmetric hetero Diels-Alder adducts. A rational for the observed enantioselectivity and conversion rate supported by computational calculations is provided.

U2 - 10.1021/acs.joc.9b00732

DO - 10.1021/acs.joc.9b00732

M3 - Journal article

C2 - 31033291

AN - SCOPUS:85066611116

VL - 84

SP - 6940

EP - 6945

JO - Journal of Organic Chemistry

JF - Journal of Organic Chemistry

SN - 0022-3263

IS - 11

ER -

ID: 231361334