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Literature DB >> 28391693

Asymmetric Total Synthesis of Lancifodilactone G Acetate.

Dong-Dong Liu¹, Tian-Wen Sun¹, Kuang-Yu Wang¹, Yong Lu¹, Su-Lei Zhang¹, Yuan-He Li¹, Yan-Long Jiang¹, Jia-Hua Chen¹, Zhen Yang^1,2.

Abstract

Asymmetric total synthesis of structurally intriguing and highly oxygenated lancifodilactone G acetate (7) has been achieved for the first time in 28 steps from a cheap commodity chemical, 2-(triisopropylsiloxy)-1,3-butadiene.

Entities: Chemical

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Year: 2017 PMID： 28391693 DOI： 10.1021/jacs.7b02561

Source DB: PubMed Journal: J Am Chem Soc ISSN： 0002-7863 Impact factor: 15.419

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Cited

6 in total

1. An Initiation Kinetics Prediction Model Enables Rational Design of Ruthenium Olefin Metathesis Catalysts Bearing Modified Chelating Benzylidenes.

Authors: Shao-Xiong Luo; Keary M Engle; Xiaofei Dong; Andrew Hejl; Michael K Takase; Lawrence M Henling; Peng Liu; K N Houk; Robert H Grubbs
Journal: ACS Catal Date: 2018-04-10 Impact factor: 13.084

2. Ring Expansion of 1-Indanones to 2-Halo-1-naphthols as an Entry Point to Gilvocarcin Natural Products.

Authors: Ivica Zamarija; Benjamin J Marsh; Thomas Magauer
Journal: Org Lett Date: 2021-11-15 Impact factor: 6.005

3. Total syntheses of schilancidilactones A and B, schilancitrilactone A, and 20-epi-schilancitrilactone A via late-stage nickel-catalyzed cross coupling.

Authors: Hengtao Wang; Xiunan Zhang; Pingping Tang
Journal: Chem Sci Date: 2017-08-30 Impact factor: 9.825

Asymmetric Total Synthesis of Lancifodilactone G Acetate.

1. An Initiation Kinetics Prediction Model Enables Rational Design of Ruthenium Olefin Metathesis Catalysts Bearing Modified Chelating Benzylidenes.

2. Ring Expansion of 1-Indanones to 2-Halo-1-naphthols as an Entry Point to Gilvocarcin Natural Products.

3. Total syntheses of schilancidilactones A and B, schilancitrilactone A, and 20-epi-schilancitrilactone A via late-stage nickel-catalyzed cross coupling.

4. Convergent Total Syntheses of (-)-Rubriflordilactone B and (-)-pseudo-Rubriflordilactone B.

Review 5. Application of Pauson-Khand reaction in the total synthesis of terpenes.

6. Total Synthesis of the Schisandraceae Nortriterpenoid Rubriflordilactone A.