Copper-Catalyzed Hydroarylation of Alkynes for the Synthesis of Fascaplysin, Rutacarpine and Granulatimide Analogues
Publication type: Journal Article
Publication date: 2015-08-21
scimago Q2
wos Q2
SJR: 0.559
CiteScore: 4.6
Impact factor: 2.3
ISSN: 00397881, 1437210X
Catalysis
Organic Chemistry
Abstract
An efficient copper-catalyzed π-activation protocol has been developed for the intramolecular hydroarylation of alkynes. The strategy has been used in atom-economical syntheses of β-carboline analogues. The cycloisomerized products were obtained in moderate to good yields.
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Vairaprakash P., Nagarajan R. Copper-Catalyzed Hydroarylation of Alkynes for the Synthesis of Fascaplysin, Rutacarpine and Granulatimide Analogues // Synthesis. 2015. Vol. 47. No. 22. pp. 3573-3582.
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Vairaprakash P., Nagarajan R. Copper-Catalyzed Hydroarylation of Alkynes for the Synthesis of Fascaplysin, Rutacarpine and Granulatimide Analogues // Synthesis. 2015. Vol. 47. No. 22. pp. 3573-3582.
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RIS
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TY - JOUR
DO - 10.1055/s-0034-1378735
UR - https://doi.org/10.1055/s-0034-1378735
TI - Copper-Catalyzed Hydroarylation of Alkynes for the Synthesis of Fascaplysin, Rutacarpine and Granulatimide Analogues
T2 - Synthesis
AU - Vairaprakash, Pothiappan
AU - Nagarajan, Rajagopal
PY - 2015
DA - 2015/08/21
PB - Georg Thieme Verlag KG
SP - 3573-3582
IS - 22
VL - 47
SN - 0039-7881
SN - 1437-210X
ER -
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BibTex (up to 50 authors)
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@article{2015_Vairaprakash,
author = {Pothiappan Vairaprakash and Rajagopal Nagarajan},
title = {Copper-Catalyzed Hydroarylation of Alkynes for the Synthesis of Fascaplysin, Rutacarpine and Granulatimide Analogues},
journal = {Synthesis},
year = {2015},
volume = {47},
publisher = {Georg Thieme Verlag KG},
month = {aug},
url = {https://doi.org/10.1055/s-0034-1378735},
number = {22},
pages = {3573--3582},
doi = {10.1055/s-0034-1378735}
}
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MLA
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Vairaprakash, Pothiappan, and Rajagopal Nagarajan. “Copper-Catalyzed Hydroarylation of Alkynes for the Synthesis of Fascaplysin, Rutacarpine and Granulatimide Analogues.” Synthesis, vol. 47, no. 22, Aug. 2015, pp. 3573-3582. https://doi.org/10.1055/s-0034-1378735.