Results 11 to 20 of about 1,737,350 (269)

Total Synthesis of (+)-Mycalamide A [PDF]

open access: yesOrganic Letters, 2006
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
Natsuko, Kagawa   +2 more
openaire   +2 more sources

Total Synthesis of (−)-Callystatin A [PDF]

open access: yesOrganic Letters, 2004
[reaction: see text] A convergent enantioselective synthesis of the natural product (-)-callystatin A (1) is described. Key features of the synthesis include a lipase-mediated kinetic resolution to install the C5 lactone stereochemistry, a hydrozirconation-based approach to the C8-C9 trisubstituted (Z)-olefin, and a stereoselective cross-coupling of a ...
Neil F, Langille, James S, Panek
openaire   +2 more sources

Novel Strategies in C-H Oxidations for Natural Product Diversification—A Remote Functionalization Application Summary

open access: yesFrontiers in Chemistry, 2021
Selectively activating the distal inactive C-H bond for functionalization is one of the on-going challenge in organic synthetic chemistry. In recent years, benefiting from the development of selective synthesis methods, novel methodologies not only make ...
Huang Junrong   +11 more
doaj   +1 more source

Total Synthesis of (+)-Cylindramide A [PDF]

open access: yesJournal of the American Chemical Society, 2006
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
Amy C, Hart, Andrew J, Phillips
openaire   +2 more sources

Total Syntheses of Mycolactone A/B and its Analogues for the Exploration of the Biology of Buruli Ulcer

open access: yesCHIMIA, 2017
Buruli ulcer, classified as a neglected tropical disease by the World Health Organization, is caused by a mycobacterium which secretes a macrolidic exotoxin called mycolactone A/B.
Sarah Saint-Auret   +6 more
doaj   +1 more source

Preparation of an advanced intermediate for the synthesis of leustroducsins and phoslactomycins by heterocycloaddition

open access: yesBeilstein Journal of Organic Chemistry, 2022
A convergent strategy for the synthesis of leustroducsins and phoslactomycins has been designed, relying on the synthesis and the coupling of three main fragments.
Anaïs Rousseau   +2 more
doaj   +1 more source

The Total Synthesis of (−)-Lemonomycin [PDF]

open access: yesJournal of the American Chemical Society, 2003
The first total synthesis of the novel glycosylated tetrahydroisoquinoline antitumor antibiotic (-)-lemonomycin has been accomplished (15 steps from 9). The highly convergent synthesis relies on a key asymmetric dipolar cycloaddition to set the stereochemistry of the aglycone core, a Suzuki fragment coupling to connect the diazabicycle to the aryl ...
Ashley, Eric R.   +2 more
openaire   +3 more sources

Synthetic Advances in Macrosphelides: Natural Anticancer Agents

open access: yesMolecules, 2014
Total synthesis of macrosphelides is summarized. Synthetic approaches contain the preparation of key fragments and the final ring-closure reaction for unique 16- or 15-membered macrolactone skeletons.
Seung-Mann Paek
doaj   +1 more source

Total Synthesis of (±)-Symbioimine [PDF]

open access: yesOrganic Letters, 2006
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
Yefen, Zou   +2 more
openaire   +3 more sources

Total synthesis of remdesivir

open access: yesTetrahedron Letters, 2022
Remdesivir, the first drug approved by the FDA to treat COVID-19, is in high demand for patients infected with the SARS-CoV-2 virus. Herein, we report a facile approach minimizing the protecting group manipulations to afford remdesivir in good overall yield.
Kumar Palli, Kishore   +9 more
openaire   +2 more sources

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