Benzenoid Aromatics from Renewable Resources

S Zheng, Z Zhang, S He, H Yang, H Atia… - Chemical …, 2024 - ACS Publications
In this Review, all known chemical methods for the conversion of renewable resources into
benzenoid aromatics are summarized. The raw materials that were taken into consideration …

Synthesis of 2-Tetrazolylmethyl-isoindolin-1-ones via a One-Pot Ugi-Azide/(N-Acylation/exo-Diels–Alder)/Dehydration Process

A Rentería-Gómez, A Islas-Jácome… - ACS …, 2016 - ACS Publications
A series of fifteen 2-tetrazolylmethyl-isoindolin-1-one linked-type bis-heterocycles were
synthesized in 10–76% yields under mild conditions via a one-pot Ugi-azide/(N …

Isoindolone formation via intramolecular Diels–Alder reaction

M Ball, A Boyd, G Churchill, M Cuthbert… - … Process Research & …, 2012 - ACS Publications
The intramolecular Diels–Alder reaction provides a useful synthetic methodology to build
biologically active and synthetically useful isoindolone ring systems. An application of this …

Synthesis of phosphonic acids possessing isoindolin-1-one moiety: Unexpected acid-catalyzed CP-bond cleavage

GO Kachkovskyi, OI Kolodiazhnyi - Phosphorus, Sulfur, and Silicon, 2009 - Taylor & Francis
Full article: Synthesis of Phosphonic Acids Possessing Isoindolin-1-one Moiety: Unexpected
Acid-Catalyzed CP-Bond Cleavage Skip to Main Content Taylor and Francis Online homepage …

Chemoselective flow hydrogenation approaches to isoindole-7-carboxylic acids and 7-oxa-bicyclio [2.2. 1] heptanes

L Hizartzidis, M Tarleton, CP Gordon, A McCluskey - RSC Advances, 2014 - pubs.rsc.org
Two libraries of highly decorated norcantharidin analogues were accessed via a series of
sequential chemoselective flow hydrogenations and solvent-free transformations. Utilising a …

Opening of the epoxide bridge in 3a,6-epoxyisoindol-1-ones by the action of BF3⋅Et2O in acetic anhydride

FI Zubkov, VP Zaytsev, ES Puzikova, EV Nikitina… - Chemistry of …, 2012 - Springer
The opening of the epoxide bridge in N-substituted 2, 3, 7, 7a-tetrahydro-3a, 6-
epoxyisoindol-1-ones by the action of BF 3⋅ Et 2 O in acetic anhydride at 25° C over 1 h …

Synthesis and antimicrobial activity of some methyl‐2‐[N‐coumarin‐6′‐yl]‐3‐oxo‐2,3‐dihydro‐1H‐isoindolone‐5‐carboxylates

AA Mir, VV Mulwad, GK Trivedi - Journal of Heterocyclic …, 2010 - Wiley Online Library
N‐substituted furylmethylimines are prepared by condensing 6‐aminocoumarins with
furfural, these on sodium borohydride reduction afford N‐[coumarin‐6′‐yl]‐2‐furylamines …

Synthesis and Structure of Esterification Products of 6-aryl-1, 2, 3, 6, 7, 7a-hexahydro-3а, 6-epoxyisoindole-7-carboxylic Acids

MА Nadirova, KM Pokazeev, IА Kolesnik… - Chemistry of …, 2019 - Springer
It was found that the reaction of 5-arylfurfurilamines with maleic anhydride leads to the
formation of 6-aryl-3a, 6-epoxyisoindole-7-carboxylic acids (the cyclic form), which in …

Synthetic transformations of higher terpenoids: XXIII. Synthesis of diterpenoid-based dihydroisoindolones

ME Mironov, YV Kharitonov, EE Shul'ts… - Russian journal of …, 2010 - Springer
Vilsmeier-Haak reaction of phlomisoic acid methyl ester gave a mixture of 15-and 16-
formyllabdanoids. In addition, methyl 2-formyldodecahydrophenanthro [1, 2-b] furan-6 …

Synthesis of 2-phosphonoheterocycles via base-promoted 5-endo cyclization

A Bousbia, ML Benkhoud, L El-Kaim, S Prévost - Tetrahedron Letters, 2021 - Elsevier
Herein, a synthesis of 2-phosphonodihydrofurans and 2-phosphonodihydropyrroles via 5-
endo cyclization of O-and N-propargylated compounds is described. The reaction is …