Molecular diversity of the reactions of MBH carbonates of isatins and various nucleophiles

• Zi-Ying Xiao,
• Jing Sun and
• Chao-Guo Yan

Beilstein J. Org. Chem. 2025, 21, 286–295, doi:10.3762/bjoc.21.21

• biologically important 3-substituted and spirooxindole derivatives [5][6][7]. The unique molecular architecture and remarkable pharmacological activities have made spirooxindole one of the hottest synthetic targets with fruitful chemical and steric selectivity [8][9][10][11][12][13][14][15]. In recent years

Thermally activated delayed fluorescence (TADF) emitters: sensing and boosting spin-flipping by aggregation

• Ashish Kumar Mazumdar,
• Gyana Prakash Nanda,
• Nisha Yadav,
• Upasana Deori,
• Upasha Acharyya,
• Bahadur Sk and
• Pachaiyappan Rajamalli

Beilstein J. Org. Chem. 2022, 18, 1177–1187, doi:10.3762/bjoc.18.122

• -p3C aggregates. Thus, a judicious choice of D–A molecular architecture is necessary to tune the solid- or aggregated-state optical properties for triplet harvesting. Fluorescence switching The lone-pair electrons of heteroatoms, such as oxygen and nitrogen, are susceptible to acidic protons [22]. BPy

Morita–Baylis–Hillman reaction of 3-formyl-9H-pyrido[3,4-b]indoles and fluorescence studies of the products

• Nisha Devi and
• Virender Singh

Beilstein J. Org. Chem. 2022, 18, 926–934, doi:10.3762/bjoc.18.92

• structure β-carboline represents a promising class of pyridoindole alkaloids with a variety of biological activities which make them interesting synthetic targets [1][2][3][4][5][6][7][8]. Alkaloids containing the β-carboline nucleus in their molecular architecture are present ubiquitously in nature and a

Constrained thermoresponsive polymers – new insights into fundamentals and applications

• Patricia Flemming,
• Alexander S. Münch,
• Andreas Fery and
• Petra Uhlmann

Beilstein J. Org. Chem. 2021, 17, 2123–2163, doi:10.3762/bjoc.17.138

All-carbon [3 + 2] cycloaddition in natural product synthesis

• Zhuo Wang and
• Junyang Liu

Beilstein J. Org. Chem. 2020, 16, 3015–3031, doi:10.3762/bjoc.16.251

• congested arrays of stereocenters within the polycyclic framework of complex natural products usually require a sophisticated synthetic planning. This issue is not trivial because only a few strategies are available for the efficient synthesis of such an intriguing molecular architecture. More importantly

Plasma membrane imaging with a fluorescent benzothiadiazole derivative

• Pedro H. P. R. Carvalho,
• Jose R. Correa,
• Karen L. R. Paiva,
• Daniel F. S. Machado,
• Jackson D. Scholten and
• Brenno A. D. Neto

Beilstein J. Org. Chem. 2019, 15, 2644–2654, doi:10.3762/bjoc.15.257

• for all tested models. Keywords: benzothiadiazole; bioprobe; cell imaging; fluorescence; mitochondria; molecular architecture; plasma membrane; Introduction The selective staining of plasma membranes is of paramount importance to study cellular processes and events associated with this dynamic

Diazocine-functionalized TATA platforms

• Roland Löw,
• Talina Rusch,
• Fynn Röhricht,
• Olaf Magnussen and
• Rainer Herges

Beilstein J. Org. Chem. 2019, 15, 1485–1490, doi:10.3762/bjoc.15.150

• Abstract Recently, it has been shown that the thermochemical cis→trans isomerization of azobenzenes is accelerated by a factor of more than 1000 by electronic coupling to a gold surface via a conjugated system with 11 bonds and a distance of 14 Å. The corresponding molecular architecture consists of a

Asymmetric Michael addition reactions catalyzed by calix[4]thiourea cyclohexanediamine derivatives

• Zheng-Yi Li,
• Hong-Xiao Tong,
• Yuan Chen,
• Hong-Kui Su,
• Tangxin Xiao,
• Xiao-Qiang Sun and
• Leyong Wang

Beilstein J. Org. Chem. 2018, 14, 1901–1907, doi:10.3762/bjoc.14.164

• unique and tunable molecular architecture together with the ease of functionalization on the lower and upper rims [24][25][26][27][28]. Interestingly, their hydrophobic cavity also exhibits phase transfer catalytic function [29]. By attaching different pendants with catalytic ability to the scaffolds

β-Hydroxy sulfides and their syntheses

• Mokgethwa B. Marakalala,
• Edwin M. Mmutlane and
• Henok H. Kinfe

Beilstein J. Org. Chem. 2018, 14, 1668–1692, doi:10.3762/bjoc.14.143

• organic compounds are, like all natural products/secondary metabolites, staggeringly diverse with respect to their natural source and their level of structural complexity. As part of their molecular architecture, sulfur can appear in the form of various functional groups and oxidation states: thiol

• of the optically active 1,5-benzothiazepines has been done by Lévai and Kiss-Szikszai [103]. Conclusion Sulfur, with its ability to exist in various oxidation states and thus various combinations with other atoms, introduces additional intriguing complexity to the molecular architecture of natural

Herpetopanone, a diterpene from Herpetosiphon aurantiacus discovered by isotope labeling

• Xinli Pan,
• Nicole Domin,
• Sebastian Schieferdecker,
• Hirokazu Kage,
• Martin Roth and
• Markus Nett

Beilstein J. Org. Chem. 2017, 13, 2458–2465, doi:10.3762/bjoc.13.242

• resemblance to cadinane-type sesquiterpenes from plants, but is structurally entirely unprecedented in bacteria. Based on its molecular architecture, a possible biosynthetic pathway is postulated. Keywords: genome mining; herpetopanone; Herpetosiphon; isotope labeling; terpene; Introduction Terpenoids

• of herpetopanone was deduced from its molecular architecture. Furthermore, candidate genes for the necessary ring formations were identified and will be the subject of future investigations. Experimental General experimental procedures The IR spectrum was recorded on a benchtop FT-IR 4100

Nitration of 5,11-dihydroindolo[3,2-b]carbazoles and synthetic applications of their nitro-substituted derivatives

• Roman A. Irgashev,
• Nikita A. Kazin,
• Gennady L. Rusinov and
• Valery N. Charushin

Beilstein J. Org. Chem. 2017, 13, 1396–1406, doi:10.3762/bjoc.13.136

• , based on a ring-fused molecular architecture, have attracted great attention of researchers in the last two decades, because of their plausible use as promising materials for thin film electronic and photonic devices [1][2][3][4][5][6]. In this context, the fused π-conjugated backbone of 5,11

Effects of solvent additive on “s-shaped” curves in solution-processed small molecule solar cells

• John A. Love,
• Shu-Hua Chou,
• Ye Huang,
• Guilllermo C. Bazan and
• Thuc-Quyen Nguyen

Beilstein J. Org. Chem. 2016, 12, 2543–2555, doi:10.3762/bjoc.12.249

• alternating electron-rich donor (D) and the electron-deficient acceptor (A) moieties so as to facilitate efficient photo-induced charge transfer and harvest a broad spectral response [9][10][11]. One such molecular architecture introduced by Bazan and co-workers can be described as a D1–A–D2–A–D1 system [12

Is conformation a fundamental descriptor in QSAR? A case for halogenated anesthetics

• Maria C. Guimarães,
• Mariene H. Duarte,
• Josué M. Silla and
• Matheus P. Freitas

Beilstein J. Org. Chem. 2016, 12, 760–768, doi:10.3762/bjoc.12.76

• structures and the corresponding bioactivities by means of molecular descriptors (MD´s). In this way, molecular architecture and substitution patterns in a series of congeneric molecules are described by calculable or empirical data having some relationship with biological activity, becoming the technique

Antibiotics from predatory bacteria

• Juliane Korp,
• María S. Vela Gurovic and
• Markus Nett

Beilstein J. Org. Chem. 2016, 12, 594–607, doi:10.3762/bjoc.12.58

• exhibit an unusual molecular architecture featuring two oxazole rings connected by a two-carbon tether and a terminal 2,4-pentadienylamine moiety. Feeding experiments as well as biosynthetic reasoning indicated that the siphonazoles originate from a mixed PKS/NRPS pathway [125]. Both bisoxazoles were

A quadruple cascade protocol for the one-pot synthesis of fully-substituted hexahydroisoindolinones from simple substrates

• Hong-Bo Zhang,
• Yong-Chun Luo,
• Xiu-Qin Hu,
• Yong-Min Liang and
• Peng-Fei Xu

Beilstein J. Org. Chem. 2016, 12, 253–259, doi:10.3762/bjoc.12.27

• . Previously, we established organocatalytic domino reactions to construct very useful molecular architectures [47][48][49][50][51][52][53][54][55][56][57][58][59][60]. Based on this past experience, we decided to develop a one-pot quadruple protocol to construct this difficult molecular architecture using

Selected synthetic strategies to cyclophanes

• Sambasivarao Kotha,
• Mukesh E. Shirbhate and
• Gopalkrushna T. Waghule

Beilstein J. Org. Chem. 2015, 11, 1274–1331, doi:10.3762/bjoc.11.142

• macrocycles. These molecules show excellent chiroptical properties such as high fluorescence quantum efficiency and a large circularly polarized luminescence dissymmetry factor. Cyclophanes are carbon-rich materials containing extensive alkyne moieties with a persistent molecular architecture. Orita and co

Synthesis of carbohydrate-scaffolded thymine glycoconjugates to organize multivalency

• Anna K. Ciuk and
• Thisbe K. Lindhorst

Beilstein J. Org. Chem. 2015, 11, 668–674, doi:10.3762/bjoc.11.75

• appropriate carbohydrate conjugation the same molecular architecture could be applied for organization of a divalent glycoconjugate (Figure 1B). We selected thymine as a photocontrollable element as it can undergo [2 + 2] photocycloaddition upon irradiation with light of hν ≥ 290 nm [5][9][10]. Furthermore

• of photocontrollable glycoconjugates will have to follow. Cartoon of a divalent carbohydrate-scaffolded molecular architecture that allows control of the flexibility of both branches by intramolecular [2 + 2] photocycloaddition (A). To attach the photocontrollable moieties (green) to the carbohydrate

• scaffold (blue), an appropriate ligation chemistry is required. Additional ligation of sugar ligands (pink) leads to the analogous divalent glycothymine glycoconjugate (B). As building blocks for this molecular architecture a mannoside scaffold (blue), thymine (green), and α-D-mannosyl ligands (pink) were

Synthesis and properties of novel star-shaped oligofluorene conjugated systems with BODIPY cores

• Clara Orofino-Pena,
• Diego Cortizo-Lacalle,
• Joseph Cameron,
• Muhammad T. Sajjad,
• Pavlos P. Manousiadis,
• Neil J. Findlay,
• Alexander L. Kanibolotsky,
• Dimali Amarasinghe,
• Peter J. Skabara,
• Tell Tuttle,
• Graham A. Turnbull and
• Ifor D. W. Samuel

Beilstein J. Org. Chem. 2014, 10, 2704–2714, doi:10.3762/bjoc.10.285

• structures [17]. A multidimensional molecular architecture provides excellent film-forming properties of the materials and an isotropic morphology of the final film. In the case of oligofluorenes with benzene [18] and truxene cores [19][20][21][22], this design methodology has yielded promising materials for

C–H-Functionalization logic guides the synthesis of a carbacyclopamine analog

• Sebastian Rabe,
• Johann Moschner,
• Marina Bantzi,
• Philipp Heretsch and
• Athanassios Giannis

Beilstein J. Org. Chem. 2014, 10, 1564–1569, doi:10.3762/bjoc.10.161

• , including medulloblastoma, basal cell carcinoma, and rhabdomyosarcoma [5][6][7][8][9][10]. The impressive biological activity combined with a unique molecular architecture and the synthetic challenge it poses already let to the first synthesis of cyclopamine by this laboratory employing C–H

Postsynthetic functionalization of glycodendrons at the focal point

• Thisbe K. Lindhorst and
• Katharina Elsner

Beilstein J. Org. Chem. 2014, 10, 1482–1487, doi:10.3762/bjoc.10.152

• frequently applied for the synthesis of multivalent glycoconjugates [6]. Dendrons resemble a branched fragment of a whole dendrimer with an orthogonal functional group (FG) at the focal point of the molecular fragment (Figure 1a). This molecular architecture comprises the possibility to anchor a multivalent

Multichromophoric sugar for fluorescence photoswitching

• Stéphane Maisonneuve,
• Rémi Métivier,
• Pei Yu,
• Keitaro Nakatani and
• Juan Xie

Beilstein J. Org. Chem. 2014, 10, 1471–1481, doi:10.3762/bjoc.10.151

• ] (compound 2, Figure 2) so as to take advantage of this sugar-based “platform” to get a specific molecular architecture and to study the energy transfer and photo-switching efficiency. To the best of our knowledge, readily available monosaccharides have been rarely used to develop multichromophoric

Design and synthesis of multivalent neoglycoconjugates by click conjugations

• Feiqing Ding,
• Li Ji,
• Ronny William,
• Hua Chai and
• Xue-Wei Liu

Beilstein J. Org. Chem. 2014, 10, 1325–1332, doi:10.3762/bjoc.10.134

• especially versatile for the effective construction of complex glycosylated structures such as clusters, dendrimers, polymers, peptides and macrocycles. In all the cases the triazole ring plays a crucial role in combining divergent units together to establish a complex molecular architecture [23][24][25][26

Molecular architecture with carbohydrate functionalized β-peptides adopting 3₁₄-helical conformation

• Nitin J. Pawar,
• Navdeep S. Sidhu,
• George M. Sheldrick,
• Dilip D. Dhavale and
• Ulf Diederichsen

Beilstein J. Org. Chem. 2014, 10, 948–955, doi:10.3762/bjoc.10.93

Unusual polymorphism in new bent-shaped liquid crystals based on biphenyl as a central molecular core

• Anna Kovářová,
• Svatopluk Světlík,
• Václav Kozmík,
• Jiří Svoboda,
• Vladimíra Novotná,
• Damian Pociecha,
• Ewa Gorecka and
• Natalia Podoliak

Beilstein J. Org. Chem. 2014, 10, 794–807, doi:10.3762/bjoc.10.75

• -shaped LC materials is most commonly based on a 1,3-disubstitued benzene and a 2,7-disubstitued naphthalene central unit to which flexible lengthening arms are joined to create mesogens with symmetrical or non-symmetrical molecular architecture. Furthermore, already in the beginning of the extensive

Preparation of new alkyne-modified ansamitocins by mutasynthesis

• Kirsten Harmrolfs,
• Lena Mancuso,
• Binia Drung,
• Florenz Sasse and
• Andreas Kirschning

Beilstein J. Org. Chem. 2014, 10, 535–543, doi:10.3762/bjoc.10.49

• that a release mechanism of the cytotoxin is part of the molecular architecture of the conjugate [31]. Disulfide linkers have shown to be well suited when utilizing the reducing power between extra- and intracellular milieus which results in cleavage and liberation of the drug. Mitomycin conjugates [32