Synthesis of Pyridoacridines through Anionic Cascade Ring Closure

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Standard

Synthesis of Pyridoacridines through Anionic Cascade Ring Closure. / Petersen, I.N.; Kristensen, Jesper Langgaard.

In: Synthesis, Vol. 46, 01.01.2014, p. 1469-1474.

Research output: Contribution to journal › Journal article › Research › peer-review

Harvard

Petersen, IN & Kristensen, JL 2014, 'Synthesis of Pyridoacridines through Anionic Cascade Ring Closure', Synthesis, vol. 46, pp. 1469-1474. https://doi.org/10.1055/s-0033-1338609

APA

Petersen, I. N., & Kristensen, J. L. (2014). Synthesis of Pyridoacridines through Anionic Cascade Ring Closure. Synthesis, 46, 1469-1474. https://doi.org/10.1055/s-0033-1338609

Vancouver

Petersen IN, Kristensen JL. Synthesis of Pyridoacridines through Anionic Cascade Ring Closure. Synthesis. 2014 Jan 1;46:1469-1474. https://doi.org/10.1055/s-0033-1338609

Author

Petersen, I.N. ; Kristensen, Jesper Langgaard. / Synthesis of Pyridoacridines through Anionic Cascade Ring Closure. In: Synthesis. 2014 ; Vol. 46. pp. 1469-1474.

Bibtex

@article{bed8e2b7a32e4d509e257c4be9eca0e3,
title = "Synthesis of Pyridoacridines through Anionic Cascade Ring Closure",
abstract = "A new synthesis of 13-deazaascididemin (AK-37) based on a recently developed anionic cascade ring closure is presented. Although the isolated yields are modest, the approach provides ready access to new substituted derivatives of 13-deazaascididemin.",
author = "I.N. Petersen and Kristensen, {Jesper Langgaard}",
year = "2014",
month = jan,
day = "1",
doi = "10.1055/s-0033-1338609",
language = "English",
volume = "46",
pages = "1469--1474",
journal = "Synthesis",
issn = "0039-7881",
publisher = "GeorgThieme Verlag",

}

RIS

TY - JOUR

T1 - Synthesis of Pyridoacridines through Anionic Cascade Ring Closure

AU - Petersen, I.N.

AU - Kristensen, Jesper Langgaard

PY - 2014/1/1

Y1 - 2014/1/1

N2 - A new synthesis of 13-deazaascididemin (AK-37) based on a recently developed anionic cascade ring closure is presented. Although the isolated yields are modest, the approach provides ready access to new substituted derivatives of 13-deazaascididemin.

AB - A new synthesis of 13-deazaascididemin (AK-37) based on a recently developed anionic cascade ring closure is presented. Although the isolated yields are modest, the approach provides ready access to new substituted derivatives of 13-deazaascididemin.

UR - http://www.scopus.com/inward/record.url?scp=84896419554&partnerID=8YFLogxK

U2 - 10.1055/s-0033-1338609

DO - 10.1055/s-0033-1338609

M3 - Journal article

VL - 46

SP - 1469

EP - 1474

JO - Synthesis

JF - Synthesis

SN - 0039-7881

ER -

ID: 105613443