Total synthesis of ascididemin via anionic cascade ring closure

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

Standard

Total synthesis of ascididemin via anionic cascade ring closure. / Petersen, Ida Nymann; Crestey, François; Kristensen, Jesper Langgaard.

In: Chemical Communications, Vol. 48, No. 72, 2012, p. 9092-9094.

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

Harvard

Petersen, IN, Crestey, F & Kristensen, JL 2012, 'Total synthesis of ascididemin via anionic cascade ring closure', Chemical Communications, vol. 48, no. 72, pp. 9092-9094. https://doi.org/10.1039/c2cc34725c

APA

Petersen, I. N., Crestey, F., & Kristensen, J. L. (2012). Total synthesis of ascididemin via anionic cascade ring closure. Chemical Communications, 48(72), 9092-9094. https://doi.org/10.1039/c2cc34725c

Vancouver

Petersen IN, Crestey F, Kristensen JL. Total synthesis of ascididemin via anionic cascade ring closure. Chemical Communications. 2012;48(72):9092-9094. https://doi.org/10.1039/c2cc34725c

Author

Petersen, Ida Nymann ; Crestey, François ; Kristensen, Jesper Langgaard. / Total synthesis of ascididemin via anionic cascade ring closure. In: Chemical Communications. 2012 ; Vol. 48, No. 72. pp. 9092-9094.

Bibtex

@article{6103935f85ac43d2acadbc23314c8fb5,
title = "Total synthesis of ascididemin via anionic cascade ring closure",
abstract = "A new and convergent synthesis of ascididemin is presented. Using an anionic cascade ring closure as the key step, this natural product is obtained in 45% overall yield in just 6 steps starting from 2'-fluoroacetophenone. This new approach was extended to the synthesis of a new isomer of ascididemin.",
author = "Petersen, {Ida Nymann} and Fran{\c c}ois Crestey and Kristensen, {Jesper Langgaard}",
year = "2012",
doi = "10.1039/c2cc34725c",
language = "English",
volume = "48",
pages = "9092--9094",
journal = "Chemical Communications",
issn = "1359-7345",
publisher = "Royal Society of Chemistry",
number = "72",

}

RIS

TY - JOUR

T1 - Total synthesis of ascididemin via anionic cascade ring closure

AU - Petersen, Ida Nymann

AU - Crestey, François

AU - Kristensen, Jesper Langgaard

PY - 2012

Y1 - 2012

N2 - A new and convergent synthesis of ascididemin is presented. Using an anionic cascade ring closure as the key step, this natural product is obtained in 45% overall yield in just 6 steps starting from 2'-fluoroacetophenone. This new approach was extended to the synthesis of a new isomer of ascididemin.

AB - A new and convergent synthesis of ascididemin is presented. Using an anionic cascade ring closure as the key step, this natural product is obtained in 45% overall yield in just 6 steps starting from 2'-fluoroacetophenone. This new approach was extended to the synthesis of a new isomer of ascididemin.

U2 - 10.1039/c2cc34725c

DO - 10.1039/c2cc34725c

M3 - Journal article

C2 - 22864261

VL - 48

SP - 9092

EP - 9094

JO - Chemical Communications

JF - Chemical Communications

SN - 1359-7345

IS - 72

ER -

ID: 40379260