Stereoselective total synthesis of dodoneine

Narsaiah, A. Venkat; J, Kranthi Kumar; K, Srinivasa Rao

doi:10.24820/ark.5550190.p011.824

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Figure 1 Amide Based Fungicides1

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2023

2024

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Cited by 4 publications

(1 citation statement)

References 30 publications

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“…As part of our regular research program in synthesis of biologically active molecules, herein we report a simple and protecting group free synthesis of mandipropamid. [14][15][16][17][18]…”

Section: Figure 1 Amide Based Fungicidesmentioning

confidence: 99%

Protecting group-free synthesis of the fungicide Mandipropamid

Narsaiah¹,

Annapurna²,

Bv³

2023

Arkivoc

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A simple and efficient protecting group free synthesis of a relatively new fungicide Mandipropamid has been achieved in five steps, with an excellent overall yield. The synthesis started from commercially available starting materials like vanillin and p-chloroacetophenone. The key steps involved in the synthesis are the Henry and Cannizzaro reactions, as well as amide formation through a carboxylic acid-amine coupling step.

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“…As part of our regular research program in synthesis of biologically active molecules, herein we report a simple and protecting group free synthesis of mandipropamid. [14][15][16][17][18]…”

Section: Figure 1 Amide Based Fungicidesmentioning

confidence: 99%

Protecting group-free synthesis of the fungicide Mandipropamid

Narsaiah¹,

Annapurna²,

Bv³

2023

Arkivoc

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Total Synthesis of Natural Products Dysideolide A and B

et al. 2023

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The total synthesis of marine sponge products dysideolide A and B have been achieved in stereo controlled manner. The butenolide and pentenolide lactones are consisting of sensitive, α,β-unsaturated cis-olefin functional group and which was installed by Still-Gennari olefination with ketone. The synthesis starts from D-mannitol and D-ribose respectively. Notable features of the synthesis are Z-selective Still-Gennari olefination, Pinnick oxidation and Shiina macrolactonization.

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Design, synthesis and insilico studies of 3-fluoro-3-substituted oxindoles against cancer targets

Ranganath

Narsaiah

2023

Journal of Fluorine Chemistry

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Stereoselective total synthesis of dodoneine

Cited by 4 publications

References 30 publications

Protecting group-free synthesis of the fungicide Mandipropamid

Protecting group-free synthesis of the fungicide Mandipropamid

Total Synthesis of Natural Products Dysideolide A and B

Design, synthesis and insilico studies of 3-fluoro-3-substituted oxindoles against cancer targets

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