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Carbocyclic galanthamine analogues: construction of the novel 6H-benzo[a]cyclohepta[hi]benzofuran ring system

Matthias Treu ¹

Matthias Treu

Johannes Froehlich ¹

Johannes Froehlich

Ulrich Jordis ¹

Ulrich Jordis

¹ Institute of Applied Synthetic Chemistry, Vienna University of Technology, Vienna, Austria

10.1070/MC2002v012n02ABEH001557

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Published 2002-04-30

Communication , Volume 12, Issue 2, 52-53

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Treu M., Froehlich J., Jordis U. Carbocyclic galanthamine analogues: construction of the novel 6H-benzo[a]cyclohepta[hi]benzofuran ring system // Mendeleev Communications. 2002. Vol. 12. No. 2. pp. 52-53.

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TY - JOUR

DO - 10.1070/MC2002v012n02ABEH001557

UR - https://mendcomm.colab.ws/publications/10.1070/MC2002v012n02ABEH001557

TI - Carbocyclic galanthamine analogues: construction of the novel 6H-benzo[a]cyclohepta[hi]benzofuran ring system

T2 - Mendeleev Communications

AU - Treu, Matthias

AU - Froehlich, Johannes

AU - Jordis, Ulrich

PY - 2002

DA - 2002/04/30

PB - Mendeleev Communications

SP - 52-53

IS - 2

VL - 12

ER -

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@article{2002_Treu,

author = {Matthias Treu and Johannes Froehlich and Ulrich Jordis},

title = {Carbocyclic galanthamine analogues: construction of the novel 6H-benzo[a]cyclohepta[hi]benzofuran ring system},

journal = {Mendeleev Communications},

year = {2002},

volume = {12},

publisher = {Mendeleev Communications},

month = {Apr},

url = {https://mendcomm.colab.ws/publications/10.1070/MC2002v012n02ABEH001557},

number = {2},

pages = {52--53},

doi = {10.1070/MC2002v012n02ABEH001557}

}

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Treu, Matthias, et al. “Carbocyclic galanthamine analogues: construction of the novel 6H-benzo[a]cyclohepta[hi]benzofuran ring system.” Mendeleev Communications, vol. 12, no. 2, Apr. 2002, pp. 52-53. https://mendcomm.colab.ws/publications/10.1070/MC2002v012n02ABEH001557.

Abstract

Unnatural analogues of the anti-Alzheimer drug (−)-galanthamine have been synthesised using K₃[Fe(CN)]₆ at the key step to construct the novel (±)-6H-benzo[a]cyclohepta[hi]benzofuran ring system via oxidative tandem cyclization.