Biomimetic Total Synthesis of Cyanosporaside Aglycons from a Single Enediyne Precursor through Site-Selectivep-Benzyne Hydrochlorination
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Total synthesis and related studies of large, strained, and bioactive natural products(Hetero)aromatics from dienynes, enediynes and enyne-allenes.Natural product analogues: towards a blueprint for analogue-focused synthesis.Metal Free Bi(hetero)aryl Synthesis: A Benzyne Truce-Smiles RearrangementOne-pot construction of sterically challenging and diverse polyarylphenols via transition-metal-free benzannulation and their potent in vitro antioxidant activity.Benzannulation of triynes to generate functionalized arenes by spontaneous incorporation of nucleophiles.
P2860
Biomimetic Total Synthesis of Cyanosporaside Aglycons from a Single Enediyne Precursor through Site-Selectivep-Benzyne Hydrochlorination
description
wetenschappelijk artikel
@nl
наукова стаття, опублікована в жовтні 2014
@uk
name
Biomimetic Total Synthesis of ...... ivep-Benzyne Hydrochlorination
@en
Biomimetic Total Synthesis of ...... ivep-Benzyne Hydrochlorination
@nl
type
label
Biomimetic Total Synthesis of ...... ivep-Benzyne Hydrochlorination
@en
Biomimetic Total Synthesis of ...... ivep-Benzyne Hydrochlorination
@nl
prefLabel
Biomimetic Total Synthesis of ...... ivep-Benzyne Hydrochlorination
@en
Biomimetic Total Synthesis of ...... ivep-Benzyne Hydrochlorination
@nl
P2093
P2860
P356
P1476
Biomimetic Total Synthesis of ...... ivep-Benzyne Hydrochlorination
@en
P2093
Ilya D. Gridnev
Masahiro Hirama
Shuji Yamashita
Takaya Yamaguchi
Yujiro Hayashi
P2860
P304
13902-13906
P356
10.1002/ANIE.201408416
P407
P577
2014-10-08T00:00:00Z