Synthesis of enantiomerically pure juglomycin C and NHAB

@article{Kamo2015SynthesisOE,
  title={Synthesis of enantiomerically pure juglomycin C and NHAB},
  author={Shogo Kamo and Sayako Maruo and Kouji Kuramochi and Kazunori Tsubaki},
  journal={Tetrahedron},
  year={2015},
  volume={71},
  pages={3478-3484}
}
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5 Citations

5 Citations

Citation Type

Citation Type

Unified Approach toward Syntheses of Juglomycins and Their Derivatives
TLDR
The spectroscopic data for synthetic juglomycin Z were not consistent with the data reported for the natural one, strongly suggesting a structural misassignment.
Polycyclic C-deoxyaminoglycoside-polyketides from an Australian Pasture Plant Derived Streptomyces sp.
The Australian plant pasture-derived Streptomyces sp. CMB-PB042 yielded the unprecedented polycyclic C-aminoglycoside-pyranonaphthoquinone polyketides glenthamine A (1) and glenthimine A (2), the…
Recent Applications in the Use of Sulfoxides as Chiral Auxiliaries for the Asymmetric Synthesis of Natural and Biologically Active Products
The contribution of chiral sulfoxides as versatile auxiliaries in the field of organic chemistry has shown a prevalent interest in the asymmetric synthesis of natural products during the last 45…
Streptavidin-Hosted Organocatalytic Aldol Addition
TLDR
The results have proven the concept that Sav can be used to host stereoselective aldol addition, and further protein engineering efforts can be included to improve the selectivity.
A Step‐Economic Synthesis of ( S )‐(−)‐Juglomycin C and ( S )‐(−)‐NHAB by Dötz Benzannulation and Convergent Deprotections

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