Results 271 to 280 of about 1,840,129 (319)
Biomimetic Total Synthesis of (±)-Lappaceolides A and B. [PDF]
Pallerla RR +3 more
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Total synthesis of natural products based on hydrogenation of aromatic rings. [PDF]
Wu H, Qi X.
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Total Synthesis of the SJG-2 Glycan: General Strategies for Constructing Sterically Congested Sialylated Glycans. [PDF]
Su YY +6 more
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Advances in Zr-mediated radical transformations and applications to total synthesis. [PDF]
Ogawa H, Nakamura H.
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Total Synthesis of Antimalarial Macrolide Strasseriolide A by Ni/Zr-Mediated Reductive Ketone Coupling. [PDF]
Umehara A, Kawakita KH, Sasaki M.
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Flow Chemistry Enabled Asymmetric Total Synthesis of (+)-Biotin through Pseudocatalytic Strategy. [PDF]
Zheng X +6 more
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Total Synthesis of Siomycin A: Completion of the Total Synthesis
Chemistry – An Asian Journal, 2008AbstractThe total synthesis of siomycin A (1), a representative compound of the thiostrepton family of peptide antibiotics, was achieved by incorporating the five synthetic segments A (2), B (3), C (4), D (5), and E (6). The dehydropiperidine segment A (2) was esterified with the dihydroquinoline segment C (4), and the subsequent coupling with the β ...
Tomonori, Mori +10 more
openaire +2 more sources
Total synthesis of (−)-raumacline
Chem. Commun., 2003AbstractFor Abstract see ChemInform Abstract in Full Text.
Bailey, Patrick D. +4 more
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Total Synthesis of (+)-Astrophylline
The Journal of Organic Chemistry, 2003The first total synthesis of (+)-astrophylline (2) has been achieved, starting from readily available enantiomerically pure (+)-(1R,4S)-4-hydroxycyclopent-2-enyl acetate (11). A novel ruthenium-catalyzed ring-closing ring-opening ring-closing metathesis of carbocyclic olefins of general type 5 was the key step, providing the stereochemically well ...
Marco, Schaudt, Siegfried, Blechert
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Total Synthesis of (+)‐Alstonlarsine A
Angewandte Chemie, 2022AbstractAn enantioselective total synthesis of (+)‐alstonlarsine A (1), a monoterpenoid indole alkaloid possessing a unique pentacyclic skeleton as well as a rare biological activity, is achieved. The key step is an efficient domino sequence, comprising enamine formation followed by an inverse‐electron‐demand intramolecular dearomative Diels–Alder ...
Zorana Ferjancic +2 more
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