Catalyst-free assembly of giant tris(heteroaryl)methanes: Synthesis of novel pharmacophoric triads and model sterically crowded tris(heteroaryl/aryl)methyl cation salts

Rodrigo Abonia; Luisa F. Gutiérrez; Braulio Insuasty; Jairo Quiroga; Kenneth K. Laali; Chunqing Zhao; Gabriela L. Borosky; Samantha M. Horwitz; Scott D. Bunge

doi:10.3762/bjoc.15.60

Catalyst-free assembly of giant tris(heteroaryl)methanes: Synthesis of novel pharmacophoric triads and model sterically crowded tris(heteroaryl/aryl)methyl cation salts

Rodrigo Abonia
, Luisa F. Gutiérrez
, Braulio Insuasty
, Jairo Quiroga
, Kenneth K. Laali
, Chunqing Zhao
, Gabriela L. Borosky
, Samantha M. Horwitz
, Scott D. Bunge

Chemistry and Biochemistry

Research output: Contribution to journal › Article › peer-review

Original language	English
Pages (from-to)	642-654
Number of pages	13
Journal	Beilstein Journal of Organic Chemistry
Volume	15
DOIs	https://doi.org/10.3762/bjoc.15.60
State	Published - Mar 12 2019

ASJC Scopus Subject Areas

Organic Chemistry

Keywords

Model heteroarylmethylium salts
Multicomponent
One-pot catalyst-free assembly
Pharmacophoric triads
Three-componen synthesis
Tris(heteroaryl)methanes
Yonemitsu-type reaction

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10.3762/bjoc.15.60

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Abonia, R., Gutiérrez, L. F., Insuasty, B., Quiroga, J., Laali, K. K., Zhao, C., Borosky, G. L., Horwitz, S. M., & Bunge, S. D. (2019). Catalyst-free assembly of giant tris(heteroaryl)methanes: Synthesis of novel pharmacophoric triads and model sterically crowded tris(heteroaryl/aryl)methyl cation salts. Beilstein Journal of Organic Chemistry, 15, 642-654. https://doi.org/10.3762/bjoc.15.60

Catalyst-free assembly of giant tris(heteroaryl)methanes: Synthesis of novel pharmacophoric triads and model sterically crowded tris(heteroaryl/aryl)methyl cation salts. / Abonia, Rodrigo; Gutiérrez, Luisa F.; Insuasty, Braulio et al.
In: Beilstein Journal of Organic Chemistry, Vol. 15, 12.03.2019, p. 642-654.

Research output: Contribution to journal › Article › peer-review

Abonia, R, Gutiérrez, LF, Insuasty, B, Quiroga, J, Laali, KK, Zhao, C, Borosky, GL, Horwitz, SM & Bunge, SD 2019, 'Catalyst-free assembly of giant tris(heteroaryl)methanes: Synthesis of novel pharmacophoric triads and model sterically crowded tris(heteroaryl/aryl)methyl cation salts', Beilstein Journal of Organic Chemistry, vol. 15, pp. 642-654. https://doi.org/10.3762/bjoc.15.60

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title = "Catalyst-free assembly of giant tris(heteroaryl)methanes: Synthesis of novel pharmacophoric triads and model sterically crowded tris(heteroaryl/aryl)methyl cation salts",

keywords = "Model heteroarylmethylium salts, Multicomponent, One-pot catalyst-free assembly, Pharmacophoric triads, Three-componen synthesis, Tris(heteroaryl)methanes, Yonemitsu-type reaction",

author = "Rodrigo Abonia and Guti{\'e}rrez, \{Luisa F.\} and Braulio Insuasty and Jairo Quiroga and Laali, \{Kenneth K.\} and Chunqing Zhao and Borosky, \{Gabriela L.\} and Horwitz, \{Samantha M.\} and Bunge, \{Scott D.\}",

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doi = "10.3762/bjoc.15.60",

language = "English",

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T2 - Synthesis of novel pharmacophoric triads and model sterically crowded tris(heteroaryl/aryl)methyl cation salts

AU - Abonia, Rodrigo

AU - Gutiérrez, Luisa F.

AU - Insuasty, Braulio

AU - Quiroga, Jairo

AU - Laali, Kenneth K.

AU - Zhao, Chunqing

AU - Borosky, Gabriela L.

AU - Horwitz, Samantha M.

AU - Bunge, Scott D.

PY - 2019/3/12

Y1 - 2019/3/12

KW - Model heteroarylmethylium salts

KW - Multicomponent

KW - One-pot catalyst-free assembly

KW - Pharmacophoric triads

KW - Three-componen synthesis

KW - Tris(heteroaryl)methanes

KW - Yonemitsu-type reaction

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UR - https://www.scopus.com/pages/publications/85064233502#tab=citedBy

U2 - 10.3762/bjoc.15.60

DO - 10.3762/bjoc.15.60

M3 - Article

AN - SCOPUS:85064233502

VL - 15

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EP - 654

JO - Beilstein Journal of Organic Chemistry

JF - Beilstein Journal of Organic Chemistry

ER -

Catalyst-free assembly of giant tris(heteroaryl)methanes: Synthesis of novel pharmacophoric triads and model sterically crowded tris(heteroaryl/aryl)methyl cation salts

ASJC Scopus Subject Areas

Keywords

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