Carbon–Carbon Bond Formation: The Petrov Synthesis of Combretastatin A-4

• Source: Organic Synthesis : State of the Art 2011-2013, 2015.

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The Thomson Synthesis of (–)-GB17

• Source: Organic Synthesis : State of the Art 2011-2013, 2015.

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Chloranthalactone (Liu), Rumphellaone A (Kuwahara), Lactiflorin (Bach), Echinosporin (Hale), Harveynone (Taylor), (6,7-deoxy)-Yuanhuapin (Wender)

• Source: Organic Synthesis : State of the Art 2011-2013, 2015.

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The Yamashita/Hirama Synthesis of Cortistatin A

• Source: Organic Synthesis : State of the Art 2011-2013, 2015.

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Natural Product Synthesis by C–H Functionalization: (–)-Zampanolide (Ghosh), Muraymycin D2 (Ichikawa), (+)-Sundiversifolide (Iwabuchi), (+)-Przewalskin B (Zhang/Tu), Artemisinin (Wu)

• Source: Organic Synthesis : State of the Art 2011-2013, 2015.

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C–H Functionalization: The Ono/Kato/Dairi Synthesis of Fusiocca-1,10(14)-diene-3,8β,16-triol

• Source: Organic Synthesis : State of the Art 2011-2013, 2015.

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Construction of Alkylated Stereocenters: The Deng Synthesis of (–)-Isoacanthodoral

• Source: Organic Synthesis : State of the Art 2011-2013, 2015.

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The Reisman Synthesis of (–)-Maoecrystal Z

• Source: Organic Synthesis : State of the Art 2011-2013, 2015.

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Functional Group Transformations

• Source: Organic Synthesis : State of the Art 2011-2013, 2015.

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Alkaloid Synthesis: (+)-Deoxoprosopinine (Krishna), Alkaloid (–)-205B (Micalizio), FR901483 (Huang), (+)-Ibophyllidine (Kwon), (–)-Lycoposerramine-S (Fukuyama), (±)-Crinine (Lautens)

• Source: Organic Synthesis : State of the Art 2011-2013, 2015.

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