Sharpless asymmetric epoxidation: Applications in the synthesis of bioactive natural products

SK Sartori, IL Miranda, MAN Diaz… - Mini-Reviews in …, 2021 - ingentaconnect.com
This review discusses an important synthetic tool proposed by KB Sharpless in 1980, known
as the Sharpless asymmetric epoxidation of allylic alcohols, and examines its use in the total …

Achmatowicz reaction: a versatile tool in bioactive natural products synthesis

P S. Mahajan, V T. Humne… - Current Organic …, 2017 - benthamdirect.com
Achmatowicz reaction has emerged as an efficient tool in organic synthesis since its
discovery in 1971 by Achmatowicz Jr. The original protocol went through several …

Cleistochlamys kirkii chemical constituents: Antibacterial activity and synergistic effects against resistant Staphylococcus aureus strains

F Pereira, AM Madureira, S Sancha, S Mulhovo… - Journal of …, 2016 - Elsevier
Abstract Ethnopharmacological relevance Cleistochlamys kirkii (Benth) Oliv.,(Annonaceae)
is a medicinal plant traditionally used in Mozambique to treat infectious diseases. Aims of …

New antitumour agents with α, β-unsaturated δ-lactone scaffold: Synthesis and antiproliferative activity of (−)-cleistenolide and analogues

G Benedeković, I Kovačević, M Popsavin… - Bioorganic & Medicinal …, 2016 - Elsevier
A stereoselective total synthesis of (−)-cleistenolide (1) from d-glucose has been achieved.
This new approach for the synthesis of (−)-cleistenolide and analogues involves a one-C …

Synthesis and antiproliferative activity of (5R)-cleistenolide and analogues

S Farkas, G Benedeković… - Journal of the Serbian …, 2023 - doiserbia.nb.rs
(5R)-Cleistenolide and a few related analogues have been synthesized starting from d-
glucose. The key steps of the synthesis included a Z-selective Wittig olefination and an …

Total synthesis of (−)-cleistenolide and formal synthesis of herbarumin I via a diastereoselective modulable allylation

P Karier, GC Catrinescu, N Diercxsens, K Robeyns… - Tetrahedron, 2018 - Elsevier
A modulable tin based allylation method for the synthesis of 1, 2, 3-triols is described. The
optimization of the reaction was aided by 1 H and 119 Sn low temperature NMR …

Sinteza I biološka aktivnost (−)-kleinstenolida I njegovih analoga

F Šandor - 2023 - search.proquest.com
U ovom radu je ostvarena nova, višefazna sinteza prirodnog laktona (-)-kleistenolida (1) i
njegovih odgovarajućih S-4, S-5 i S-6 analoga. Pored toga, ispitivana je biološka aktivnost …

Sinteza i biološka aktivnost (−)-kleinstenolida i njegovih analoga

Ш Фаркаш - Универзитет у Новом Саду, 2023 - nardus.mpn.gov.rs
U ovom radu je ostvarena nova, višefazna sinteza prirodnog laktona (-)-kleistenolida (1) i
njegovih odgovarajućih S-4, S-5 i S-6 analoga. Pored toga, ispitivana je biološka aktivnost …

[PDF][PDF] Sharpless Asymmetric Epoxidation: Important Contributions to the Synthesis of Biologically ActiveNatural Products

SK Sartori, IL Miranda, MAN Diaz, G Diaz-Muñoz - researchgate.net
This review discusses an important synthetic tool proposed by KB Sharpless in 1980, known
as the Sharpless asymmetric epoxidation of allylic alcohols, and examines its use in the total …

Synthetic Studies toward (−)-Cleistenolide: Highly Stereoselective Synthesis of New γ-Lactone Subunits

SK Sartori, IL Miranda, DA Matos, M Kohlhoff… - Journal of the Brazilian …, 2021 - SciELO Brasil
This study describes the stereoselective synthesis of two new γ-lactones in 6 and 3 steps
and 19 and 32% yield, respectively, directed toward the total synthesis of the natural product …