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25 Results Found

  • Review
  • Open Access
1 Citations
1,271 Views
19 Pages

15 October 2025

This review highlights enantioselective strategies for preparing (N,O)- (N,N)- and (N,S)-spiroketal skeleton, which are key structural units found in many natural products and pharmacologically active substances. The strategies are mainly based on me...

(This article belongs to the Special Issue Synthetic Studies Aimed at Heterocyclic Organic Compounds, 2nd Edition)
  • Article
  • Open Access
3 Citations
2,390 Views
9 Pages

Hyperacmosin R, a New Decarbonyl Prenylphloroglucinol with Unusual Spiroketal Subunit from Hypericum acmosepalum

  • Yonghui Ma,
  • Xiaoyu Liu,
  • Bo Liu,
  • Pingping Li,
  • Xinyue Suo,
  • Tingting Zhu,
  • Tengfei Ji,
  • Jin Li and
  • Xiaoxiu Li

13 September 2022

Two previously undescribed polycyclic polyprenylated acylphloroglucinols, hyperacmosins R-S (1–2), were obtained from the aerial parts of Hypericum acmosepalum. Their structures were elucidated by extensive spectroscopic analysis and electronic...

(This article belongs to the Section Natural Products Chemistry)
  • Review
  • Open Access
87 Citations
20,083 Views
97 Pages

28 August 2008

Spiroketals are widely found as substructures of many naturally occurring compounds from diverse sources including plants, animals as well as microbes. Naturally occurring spiroketals are biologically active and most of them are chiral molecules. Thi...

(This article belongs to the Special Issue Spiro Compounds)
  • Review
  • Open Access
41 Citations
15,438 Views
12 Pages

Nitroalkanes as Central Reagents in the Synthesis of Spiroketals

  • Roberto Ballini,
  • Marino Petrini and
  • Goffredo Rosini

7 February 2008

Nitroalkanes can be profitably employed as carbanionic precursors for theassembly of dihydroxy ketone frameworks, suitable for the preparation of spiroketals. Thecarbon-carbon bond formation is carried out exploiting nitroaldol and Michael reactions,...

(This article belongs to the Special Issue Spiro Compounds)
  • Article
  • Open Access
1 Citations
1,307 Views
13 Pages

Goondoxazoles A–C: Anthelmintic Spiroketal Polyketide Alkaloids and Other Benzoxazoles from Australian Pasture Soil-Derived Streptomyces spp.

  • Shengbin Jin,
  • David F. Bruhn,
  • Erica J. Burkman,
  • Cynthia T. Childs,
  • Jianying Han,
  • Zeinab G. Khalil,
  • Yovany Moreno,
  • Angela A. Salim,
  • Kaumadi Samarasekera and
  • Robert J. Capon
  • + 1 author

Background/Objectives/Methods: A bioassay-informed investigation of the Australian pasture soil-derived Streptomyces sp. S4S-00193A39 yielded the anthelmintic principals as three new spiroketal polyketide alkaloids, goondoxazoles A–C (1–3...

(This article belongs to the Collection Synthetic and Natural Products-Based Antimicrobial and Antiparasitic Agents)
  • Review
  • Open Access
64 Citations
21,052 Views
31 Pages

Recent Synthetic Approaches Toward Non-anomeric Spiroketals in Natural Products

  • Sylvain Favre,
  • Pierre Vogel and
  • Sandrine Gerber-Lemaire

17 October 2008

Many natural products of biological interest contain [6,5]- and [6,6]-spiroketal moieties that can adopt various configurations, benefiting or not from anomeric conformation stabilizing effects. The spiroketal fragments are often important for the bi...

(This article belongs to the Special Issue Spiro Compounds)
  • Article
  • Open Access
15 Citations
7,415 Views
14 Pages

Didemnaketals F and G, New Bioactive Spiroketals from a Red Sea Ascidian Didemnum Species

  • Lamiaa A. Shaala,
  • Diaa T.A. Youssef,
  • Sabrin R.M. Ibrahim,
  • Gamal A. Mohamed,
  • Jihan M. Badr,
  • April L. Risinger and
  • Susan L. Mooberry

25 September 2014

In continuation of our ongoing efforts to identify bioactive compounds from Red Sea marine organisms, a new collection of the ascidian Didemnum species was investigated. Chromatographic fractionation and HPLC purification of the CH2Cl2 fraction of an...

  • Article
  • Open Access
21 Citations
7,024 Views
14 Pages

Sargassopenillines A–G, 6,6-Spiroketals from the Alga-Derived Fungi Penicillium thomii and Penicillium lividum

  • Olesya I. Zhuravleva,
  • Maria P. Sobolevskaya,
  • Shamil Sh. Afiyatullov,
  • Natalya N. Kirichuk,
  • Vladimir A. Denisenko,
  • Pavel S. Dmitrenok,
  • Ekaterina A. Yurchenko and
  • Sergey A. Dyshlovoy

9 December 2014

Seven new 6,6-spiroketals, sargassopenillines A–G (1–7) were isolated from the alga-derived fungi Penicillium thomii KMM 4645 and Penicillium lividum KMM 4663. The structures of these metabolites were determined by HR-MS and 1D and 2D NMR. The absolu...

  • Article
  • Open Access
5 Citations
2,331 Views
13 Pages

HIV-1 Integrase Inhibition Activity by Spiroketals Derived from Plagius flosculosus, an Endemic Plant of Sardinia (Italy) and Corsica (France)

  • Cinzia Sanna,
  • Brigida D’Abrosca,
  • Antonio Fiorentino,
  • Federica Giammarino,
  • Ilaria Vicenti,
  • Angela Corona,
  • Alessia Caredda,
  • Enzo Tramontano and
  • Francesca Esposito

8 August 2023

In this work we investigated, for the first time, the effect of Plagius flosculosus (L.) Alavi & Heywood, a Sardinian–Corsican endemic plant, on HIV-1 integrase (IN) activity. The phytochemical analysis of the leaves chloroform extract led...

(This article belongs to the Special Issue Antiviral Compounds in Medicinal Plants 2023)
  • Article
  • Open Access
8 Citations
9,788 Views
6 Pages

Synthesis of a Novel D-Glucose-Conjugated 15-Crown-5 Ether with a Spiro Ketal Structure

  • Takashi Yamanoi,
  • Yoshiki Oda,
  • Hitomi Muraishi and
  • Sho Matsuda

22 August 2008

This paper describes a synthetic approach to a novel D-glucose-conjugated 15-crown-5 ether having a spiroketal structure starting from a 1-C-vinylated glucose derivative. The approach consists of the glycosylation of the vinylated glucose derivative...

(This article belongs to the Special Issue Spiro Compounds)
  • Review
  • Open Access
7 Citations
5,469 Views
31 Pages

24 January 2025

In spite of the many chemical reports on polyacetylenes of the genus Artemisia, combined conclusions regarding their distribution and biological functions are widely missing. The aim of the present review was to arrange the diversity of polyacetylene...

  • Review
  • Open Access
37 Citations
18,537 Views
31 Pages

Chemical and Enzymatic Approaches to Carbohydrate-Derived Spiroketals: Di-D-Fructose Dianhydrides (DFAs)

  • M. Isabel García-Moreno,
  • Juan M. Benito,
  • Carmen Ortiz Mellet and
  • José M. García Fernández

12 August 2008

Di-D-fructose dianhydrides (DFAs) comprise a unique family of stereoisomeric spiro-tricyclic disaccharides formed upon thermal and/or acidic activation of sucroseand/ or D-fructose-rich materials. The recent discovery of the presence of DFAs in food...

(This article belongs to the Special Issue Spiro Compounds)
  • Article
  • Open Access
1 Citations
1,712 Views
15 Pages

A Novel Bis-Spiroketal Scaffold and Other Secondary Metabolites from the Marine-Derived Fungus Talaromyces stipitatus HF05001: Structural Diversity and Bioactivities

  • Longhe Yang,
  • Yan Qiu,
  • Ying Liu,
  • Xiaoyu Wei,
  • Xiwen He,
  • Yiling Wang,
  • Yajun Yan,
  • Kaikai Bai,
  • Zhaokai Wang and
  • Jie Ren

19 January 2026

Marine-derived fungi have become a vital resource for the discovery of novel secondary metabolites with diverse structures and significant biological activities. This study focuses on a systematic chemical investigation of the sponge-associated fungu...

(This article belongs to the Section Structural Studies on Marine Natural Products)
  • Article
  • Open Access
16 Citations
5,364 Views
11 Pages

Constituents of the Roots of Dichapetalum pallidum and Their Anti-Proliferative Activity

  • Dorcas Osei-Safo,
  • Godwin Akpeko Dziwornu,
  • Regina Appiah-Opong,
  • Mary Anti Chama,
  • Isaac Tuffour,
  • Reiner Waibel,
  • Richard Amewu and
  • Ivan Addae-Mensah

As part of our search for bioactive compounds from the Dichapetalaceae, repeated chromatographic purification of the roots of a hitherto unexamined species, Dichapetalum pallidum, led to the isolation of the newly occurring 7-hydroxydichapetalin P (1...

(This article belongs to the Special Issue Natural Product: A Continuing Source of Novel Drug Leads)
  • Article
  • Open Access
7 Citations
4,597 Views
8 Pages

Two-step Synthesis of Solasodine Pivalate from Diosgenin Pivalate

  • Agnieszka Wojtkielewicz,
  • Urszula Kiełczewska and
  • Jacek W. Morzycki

21 March 2019

A two-step synthesis of solasodine pivalate from diosgenin pivalate is described. The key transformation involves the reaction of diosgenin pivalate with benzyl carbamate (CbzNH2) promoted by TMSOTf. During the reaction the F-ring of the spiroketal m...

(This article belongs to the Special Issue Steroids-II)
  • Article
  • Open Access
3 Citations
3,381 Views
11 Pages

Synthesis of Demissidine Analogues from Tigogenin via Imine Intermediates

  • Agnieszka Wojtkielewicz,
  • Urszula Kiełczewska,
  • Aneta Baj and
  • Jacek W. Morzycki

8 October 2021

A five-step transformation of a spiroketal side chain of tigogenin into an indolizidine system present in solanidane alkaloids such as demissidine and solanidine was elaborated. The key intermediate in the synthesis was spiroimine 3 readily obtained...

(This article belongs to the Special Issue Theme Issue Honoring Prof. Dr. Ludger Wessjohann’s 60th Birthday: Natural Products in Modern Drug Discovery)
  • Article
  • Open Access
6 Citations
4,655 Views
15 Pages

New Polyketide Congeners with Antibacterial Activities from an Endophytic Fungus Stemphylium globuliferum 17035 (China General Microbiological Culture Collection Center No. 40666)

  • Yingying Li,
  • Guoliang Zhu,
  • Jing Wang,
  • Junjie Yu,
  • Ke Ye,
  • Cuiping Xing,
  • Biao Ren,
  • Bin Zhu,
  • Simin Chen and
  • Jingyu Zhang
  • + 5 authors

24 October 2024

Four new polyketides, heterocornol Y (1), stemphyindan (2), pestalospirane C (3), and stemphyspyrane (4), along with five known ones (5–9) were isolated from the endophytic fungus Stemphylium globuliferum 17035 (SG17035) based on the One Strain...

(This article belongs to the Special Issue Advances in Fungal Endophyte Research)
  • Article
  • Open Access
10 Citations
5,222 Views
12 Pages

A Structural Analysis of the Angucycline-Like Antibiotic Auricin from Streptomyces lavendulae Subsp. Lavendulae CCM 3239 Revealed Its High Similarity to Griseusins

  • Maria Matulova,
  • Lubomira Feckova,
  • Renata Novakova,
  • Erik Mingyar,
  • Dominika Csolleiova,
  • Martina Zduriencikova,
  • Jan Sedlak,
  • Vladimir Patoprsty,
  • Vlasta Sasinkova and
  • Jan Kormanec
  • + 4 authors

We previously identified the aur1 gene cluster in Streptomyces lavendulae subsp. lavendulae CCM 3239 (formerly Streptomyces aureofaciens CCM 3239), which is responsible for the production of the angucycline-like antibiotic auricin (1). Preliminary ch...

(This article belongs to the Special Issue Mechanism and Regulation of Antibiotic Synthesis in Streptomyces)
  • Article
  • Open Access
8 Citations
5,664 Views
15 Pages

3 October 2021

Tomatidine has recently generated a lot of interest amongst the pharmacology, medicine, and biology fields of study, especially for its newfound activity as an antibiotic agent capable of targeting multiple strains of bacteria. In the light of its lo...

(This article belongs to the Special Issue Total Synthesis of Natural Products)
  • Article
  • Open Access
27 Citations
5,275 Views
10 Pages

Homo/Hetero-Dimers of Aromatic Bisabolane Sesquiterpenoids with Neuroprotective Activity from the Fungus Aspergillus versicolor A18 from South China Sea

  • Han-Zhuang Weng,
  • Jun-Yu Zhu,
  • Fang-Yu Yuan,
  • Zhuo-Ya Tang,
  • Xiao-Qing Tian,
  • Ye Chen,
  • Cheng-Qi Fan,
  • Gui-Hua Tang and
  • Sheng Yin

13 May 2022

Chromatographic fractionation of the EtOH extracts of the marine-derived fungus Aspergillus versicolor A18 has led to the isolation of 11 homo/hetero-dimers of aromatic bisabolane sesquiterpenoids including eight diphenyl ether-coupled aromatic...

(This article belongs to the Special Issue Bioactive Compounds from the Deep-Sea-Derived Microorganisms)
  • Article
  • Open Access
34 Citations
4,197 Views
13 Pages

New Polyketides from Mangrove Endophytic Fungus Penicillium sp. BJR-P2 and Their Anti-Inflammatory Activity

  • Chen Chen,
  • Geting Ye,
  • Jing Tang,
  • Jialin Li,
  • Wenbin Liu,
  • Li Wu and
  • Yuhua Long

18 September 2022

Four new polyketide compounds, including two new unique isocoumarins penicillol A (1) and penicillol B (2) featuring with spiroketal rings, two new citreoviridin derivatives citreoviridin H (3) and citreoviridin I (4), along with four known analogues...

(This article belongs to the Special Issue Diversity of Marine Fungi as a Source of Bioactive Natural Products)
  • Review
  • Open Access
60 Citations
18,534 Views
51 Pages

21 January 2010

Calyculins, highly cytotoxic polyketides, originally isolated from the marine sponge Discodermia calyx by Fusetani and co-workers, belong to the lithistid sponges group. These molecules have become interesting targets for cell biologists and syntheti...

(This article belongs to the Special Issue Synthesis around Marine Natural Products)
  • Feature Paper
  • Article
  • Open Access
10 Citations
3,866 Views
21 Pages

Mass Spectrometry-Based Characterization of New Spirolides from Alexandrium ostenfeldii (Dinophyceae)

  • Joyce A. Nieva,
  • Jan Tebben,
  • Urban Tillmann,
  • Sylke Wohlrab and
  • Bernd Krock

2 October 2020

Spirolides belong to a group of marine phycotoxins produced by the marine planktonic dinophyte Alexandrium ostenfeldii. Composed of an imine moiety and a spiroketal ring system within a macrocylcle, spirolides are highly diverse with toxin types that...

(This article belongs to the Special Issue Taking On the Challenges of Marine Natural Products Structure Elucidation)
  • Article
  • Open Access
10 Citations
3,719 Views
20 Pages

Chromatographic Separation of Breynia retusa (Dennst.) Alston Bark, Fruit and Leaf Constituents from Bioactive Extracts

  • Stefano Dall’Acqua,
  • Kouadio Ibrahime Sinan,
  • Irene Ferrarese,
  • Stefania Sut,
  • Kouadio Bene,
  • Mohamad Fawzi Mahomoodally,
  • Nabeelah Bibi Sadeer,
  • Gunes Ak and
  • Gokhan Zengin

25 November 2020

Breynia retusa (Dennst.) Alston (also known as Cup Saucer plant) is a food plant with wide applications in traditional medicine, particularly in Ayurveda. Extracts obtained with four solvents (dichloromethane, methanol, ethyl acetate and water), from...

(This article belongs to the Special Issue Chromatographic Science of Natural Products II)
  • Article
  • Open Access
569 Views
11 Pages

Background: Doramectin (CHC-B1) is an excellent antiparasitic drug produced by feeding cyclohexanecarboxylic acid (CHC) to Streptomycesavermitilis bkd− mutants. AveC, a bifunctional enzyme encoded by aveC (sav_0940), catalyzes the stereospecifi...

(This article belongs to the Section Microbiology and Ecological Metabolomics)