Results 121 to 130 of about 1,948,471 (339)

Performance Practice Bibliography (1992) [PDF]

open access: yes, 1993
A bibliography of performance practice study from the year ...

core   +1 more source

Eperua oleifera Ducke (Fabaceae) Oilresin Chemical Composition and the Isolation of a Natural Diterpenic Acid Methyl Ester

open access: yesChemistry &Biodiversity, EarlyView.
Eperua oleifera (Fabaceae) oilresin presents not only diterpenic acids, but also diterpenic acid methyl ester. ABSTRACT Eperua oleifera Ducke, commonly known as “copaíba‐jacaré,” produces oilresins traditionally used in folk medicine for wound healing and as antifungal and antibacterial agents, similar to those of Copaifera species.
Rayssa Ribeiro   +5 more
wiley   +1 more source

Oxygenated Solanapyrone Analogs From Nigrospora sp. IQ‐064, a Mangrove Associated Fungus

open access: yesChemistry &Biodiversity, EarlyView.
ABSTRACT Two new oxygenated solanapyrone analogues, nigrosporapyrone E (1) and nigrosporapyrone F (2), were isolated from Nigrospora sp. strain IQ‐064, a fungus associated with the bark of black mangrove (Avicennia germinans L.), along with seven known compounds.
Carlos A. Fajardo‐Hernández   +4 more
wiley   +1 more source

A Workflow for Selecting, Profiling, and Optimizing Plant Extracts for Cosmetic Applications

open access: yesChemistry &Biodiversity, EarlyView.
ABSTRACT In response to the growing demand for innovative natural ingredients in cosmetics, this study proposes a structured approach to identifying bioactive plant species available in France. From 1614 species screened for regulatory acceptability and innovation potential, 18 were shortlisted for phytochemical profiling (high‐performance liquid ...
Maria Viéytez   +4 more
wiley   +1 more source

Bibliographic dataset characterizing studies that use online biodiversity databases

open access: green, 2019
Joan Damerow   +8 more
openalex   +1 more source

Synthesis of α‐Pentafluorosulfanylated‐β2,3‐Amino Esters

open access: yesChemistryEurope, EarlyView.
De novo α‐SF5‐β2,3‐amino esters are now accessible through a straightforward aza‐Michael reaction using a series of newly developed (E)‐α‐SF5‐α,β‐unsaturated esters. Two new, highly functionalized, contiguous tertiary stereocenters are formed with diastereodivergence governed by the choice of solvent and/or base.
Thi Mo Nguyen   +5 more
wiley   +1 more source

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