Consecutive four-component synthesis of trisubstituted 3-iodoindoles by an alkynylation–cyclization–iodination–alkylation sequence
- Nadia Ledermann,
- Alae-Eddine Moubsit and
- Thomas J. J. Müller
Beilstein J. Org. Chem. 2023, 19, 1379–1385, doi:10.3762/bjoc.19.99
Emission solvatochromic, solid-state and aggregation-induced emissive α-pyrones and emission-tuneable 1H-pyridines by Michael addition–cyclocondensation sequences
- Natascha Breuer,
- Irina Gruber,
- Christoph Janiak and
- Thomas J. J. Müller
Beilstein J. Org. Chem. 2019, 15, 2684–2703, doi:10.3762/bjoc.15.262
Multicomponent reactions III
- Thomas J. J. Müller
Beilstein J. Org. Chem. 2019, 15, 1974–1975, doi:10.3762/bjoc.15.192
One-pot activation–alkynylation–cyclization synthesis of 1,5-diacyl-5-hydroxypyrazolines in a consecutive three-component fashion
- Christina Görgen,
- Katharina Boden,
- Guido J. Reiss,
- Walter Frank and
- Thomas J. J. Müller
Beilstein J. Org. Chem. 2019, 15, 1360–1370, doi:10.3762/bjoc.15.136
One-pot syntheses of blue-luminescent 4-aryl-1H-benzo[f]isoindole-1,3(2H)-diones by T3P® activation of 3-arylpropiolic acids
- Melanie Denißen,
- Alexander Kraus,
- Guido J. Reiss and
- Thomas J. J. Müller
Beilstein J. Org. Chem. 2017, 13, 2340–2351, doi:10.3762/bjoc.13.231
Energy down converting organic fluorophore functionalized mesoporous silica hybrids for monolith-coated light emitting diodes
- Markus Börgardts and
- Thomas J. J. Müller
Beilstein J. Org. Chem. 2017, 13, 768–778, doi:10.3762/bjoc.13.76
Thiophene-forming one-pot synthesis of three thienyl-bridged oligophenothiazines and their electronic properties
- Dominik Urselmann,
- Konstantin Deilhof,
- Bernhard Mayer and
- Thomas J. J. Müller
Beilstein J. Org. Chem. 2016, 12, 2055–2064, doi:10.3762/bjoc.12.194
The unexpected influence of aryl substituents in N-aryl-3-oxobutanamides on the behavior of their multicomponent reactions with 5-amino-3-methylisoxazole and salicylaldehyde
- Volodymyr V. Tkachenko,
- Elena A. Muravyova,
- Sergey M. Desenko,
- Oleg V. Shishkin,
- Svetlana V. Shishkina,
- Dmytro O. Sysoiev,
- Thomas J. J. Müller and
- Valentin A. Chebanov
Beilstein J. Org. Chem. 2014, 10, 3019–3030, doi:10.3762/bjoc.10.320
The Ugi four-component reaction as a concise modular synthetic tool for photo-induced electron transfer donor-anthraquinone dyads
- Sarah Bay,
- Gamall Makhloufi,
- Christoph Janiak and
- Thomas J. J. Müller
Beilstein J. Org. Chem. 2014, 10, 1006–1016, doi:10.3762/bjoc.10.100
Rapid pseudo five-component synthesis of intensively blue luminescent 2,5-di(hetero)arylfurans via a Sonogashira–Glaser cyclization sequence
- Fabian Klukas,
- Alexander Grunwald,
- Franziska Menschel and
- Thomas J. J. Müller
Beilstein J. Org. Chem. 2014, 10, 672–679, doi:10.3762/bjoc.10.60
One-pot three-component synthesis and photophysical characteristics of novel triene merocyanines
- Christian Muschelknautz,
- Robin Visse,
- Jan Nordmann and
- Thomas J. J. Müller
Beilstein J. Org. Chem. 2014, 10, 599–612, doi:10.3762/bjoc.10.51
Multicomponent reactions II
- Thomas J. J. Müller
Beilstein J. Org. Chem. 2014, 10, 115–116, doi:10.3762/bjoc.10.7
Pseudo five-component synthesis of 2,5-di(hetero)arylthiophenes via a one-pot Sonogashira–Glaser cyclization sequence
- Dominik Urselmann,
- Dragutin Antovic and
- Thomas J. J. Müller
Beilstein J. Org. Chem. 2011, 7, 1499–1503, doi:10.3762/bjoc.7.174
One-pot four-component synthesis of pyrimidyl and pyrazolyl substituted azulenes by glyoxylation–decarbonylative alkynylation–cyclocondensation sequences
- Charlotte F. Gers,
- Julia Rosellen,
- Eugen Merkul and
- Thomas J. J. Müller
Beilstein J. Org. Chem. 2011, 7, 1173–1181, doi:10.3762/bjoc.7.136
Multicomponent reactions
- Thomas J. J. Müller
Beilstein J. Org. Chem. 2011, 7, 960–961, doi:10.3762/bjoc.7.107
Synthesis, electronic properties and self-assembly on Au{111} of thiolated (oligo)phenothiazines
- Adam W. Franz,
- Svetlana Stoycheva,
- Michael Himmelhaus and
- Thomas J. J. Müller
Beilstein J. Org. Chem. 2010, 6, No. 72, doi:10.3762/bjoc.6.72
