Cargando…
Stereoselective Synthesis of the C1–C16 Fragment of the Purported Structure of Formosalide B
[Image: see text] The first stereoselective synthesis of the C1–C16 fragment possessing stereo-enriched fully substituted tetrahydropyran (THP) along with tetrahydrofuran (THF) rings of the proposed structure of formosalide B is described in 12 longest linear steps with 22% overall yield, starting f...
Autores principales: | Gajula, Srinivas, Vishnu V. Reddy, Aedula, Reddy, D. Prabhakar, Yadav, Jhillu S., Mohapatra, Debendra K. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2020
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7203982/ https://www.ncbi.nlm.nih.gov/pubmed/32391510 http://dx.doi.org/10.1021/acsomega.0c01474 |
Ejemplares similares
-
Stereoselective synthesis of four possible isomers of streptopyrrolidine
por: Mohapatra, Debendra K, et al.
Publicado: (2011) -
The Formosalides: Structure Determination by Total Synthesis
por: Schulthoff, Saskia, et al.
Publicado: (2020) -
Stereoselective synthesis of the C79–C97 fragment of symbiodinolide
por: Takamura, Hiroyoshi, et al.
Publicado: (2013) -
Stereoselective Total Syntheses of Acutifolone A,
Bisacutifolone A and B, Pinguisenol, and Isonaviculol
por: Yadav, Jhillu Singh, et al.
Publicado: (2018) -
Sub-cellular internalization and organ specific oral elivery of PABA nanoparticles by side chain variation
por: Yadav, Jhillu S, et al.
Publicado: (2011)