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8 in total

1. Late-stage intermolecular CH activation for lead diversification: a highly chemoselective oxyfunctionalization of the C-9 position of potent bryostatin analogues.

Authors: Paul A Wender; Michael K Hilinski; Alexander V W Mayweg
Journal: Org Lett Date: 2005-01-06 Impact factor: 6.005

2. Enantiospecific total synthesis of the hapalindoles, fischerindoles, and welwitindolinones via a redox economic approach.

Authors: Jeremy M Richter; Yoshihiro Ishihara; Takeshi Masuda; Brandon W Whitefield; Tomás Llamas; Antti Pohjakallio; Phil S Baran
Journal: J Am Chem Soc Date: 2008-12-31 Impact factor: 15.419

3. Total synthesis of eudesmane terpenes by site-selective C-H oxidations.

Authors: Ke Chen; Phil S Baran
Journal: Nature Date: 2009-05-13 Impact factor: 49.962

4. Chemoselectivity: the mother of invention in total synthesis.

Authors: Ryan A Shenvi; Daniel P O'Malley; Phil S Baran
Journal: Acc Chem Res Date: 2009-04-21 Impact factor: 22.384

Review 5. Catalytic C-H functionalization by metal carbenoid and nitrenoid insertion.

Authors: Huw M L Davies; James R Manning
Journal: Nature Date: 2008-01-24 Impact factor: 49.962

6. (+)-saxitoxin: a first and second generation stereoselective synthesis.

Authors: James J Fleming; Matthew D McReynolds; J Du Bois
Journal: J Am Chem Soc Date: 2007-07-21 Impact factor: 15.419

7. A predictably selective aliphatic C-H oxidation reaction for complex molecule synthesis.

Authors: Mark S Chen; M Christina White
Journal: Science Date: 2007-11-02 Impact factor: 47.728

8. Combined C-H activation/cope rearrangement as a strategic reaction in organic synthesis: total synthesis of (-)-colombiasin a and (-)-elisapterosin B.

Authors: Huw M L Davies; Xing Dai; Matthew S Long
Journal: J Am Chem Soc Date: 2006-02-22 Impact factor: 15.419

8 in total

4 in total

Organic chemistry: Synthetic lessons from nature.

1. Late-stage intermolecular CH activation for lead diversification: a highly chemoselective oxyfunctionalization of the C-9 position of potent bryostatin analogues.

2. Enantiospecific total synthesis of the hapalindoles, fischerindoles, and welwitindolinones via a redox economic approach.

3. Total synthesis of eudesmane terpenes by site-selective C-H oxidations.

4. Chemoselectivity: the mother of invention in total synthesis.

Review 5. Catalytic C-H functionalization by metal carbenoid and nitrenoid insertion.

6. (+)-saxitoxin: a first and second generation stereoselective synthesis.

7. A predictably selective aliphatic C-H oxidation reaction for complex molecule synthesis.

8. Combined C-H activation/cope rearrangement as a strategic reaction in organic synthesis: total synthesis of (-)-colombiasin a and (-)-elisapterosin B.

1. Molecular diversity and natural products.

2. Natural products version 2.0: connecting genes to molecules.

3. In silico profiling of Escherichia coli and Saccharomyces cerevisiae as terpenoid factories.

4. Electrophotocatalytic Undirected C-H Trifluoromethylations of (Het)Arenes.