Method for synthesis of 12H-pyrido[1,2-a:3,4-b']diindoles. Total synthesis of homofascaplysin C
Publication type: Journal Article
Publication date: 1996-07-01
scimago Q3
wos Q3
SJR: 0.334
CiteScore: 3.2
Impact factor: 1.5
ISSN: 00404039, 18733581
Organic Chemistry
Drug Discovery
Biochemistry
Abstract
An efficient synthesis of a 12H-pyrido[1,2-a:3,4-b']diindole system is proposed. 3-Methylindole has been converted into homofascaplysin C by a four reaction sequence in which the last step is dehydrogenation and oxidation of the methyl- to formyl group at the same time.
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Total citations:
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Citations from 2024:
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(9%)
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GOST
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Dubovitskii S. V. Method for synthesis of 12H-pyrido[1,2-a:3,4-b']diindoles. Total synthesis of homofascaplysin C // Tetrahedron Letters. 1996. Vol. 37. No. 29. pp. 5207-5208.
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Dubovitskii S. V. Method for synthesis of 12H-pyrido[1,2-a:3,4-b']diindoles. Total synthesis of homofascaplysin C // Tetrahedron Letters. 1996. Vol. 37. No. 29. pp. 5207-5208.
Cite this
RIS
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TY - JOUR
DO - 10.1016/0040-4039(96)01052-0
UR - https://doi.org/10.1016/0040-4039(96)01052-0
TI - Method for synthesis of 12H-pyrido[1,2-a:3,4-b']diindoles. Total synthesis of homofascaplysin C
T2 - Tetrahedron Letters
AU - Dubovitskii, Sergey V.
PY - 1996
DA - 1996/07/01
PB - Elsevier
SP - 5207-5208
IS - 29
VL - 37
SN - 0040-4039
SN - 1873-3581
ER -
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BibTex (up to 50 authors)
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@article{1996_Dubovitskii,
author = {Sergey V. Dubovitskii},
title = {Method for synthesis of 12H-pyrido[1,2-a:3,4-b']diindoles. Total synthesis of homofascaplysin C},
journal = {Tetrahedron Letters},
year = {1996},
volume = {37},
publisher = {Elsevier},
month = {jul},
url = {https://doi.org/10.1016/0040-4039(96)01052-0},
number = {29},
pages = {5207--5208},
doi = {10.1016/0040-4039(96)01052-0}
}
Cite this
MLA
Copy
Dubovitskii, Sergey V.. “Method for synthesis of 12H-pyrido[1,2-a:3,4-b']diindoles. Total synthesis of homofascaplysin C.” Tetrahedron Letters, vol. 37, no. 29, Jul. 1996, pp. 5207-5208. https://doi.org/10.1016/0040-4039(96)01052-0.