Enantioselective Total Synthesis of (+)-Salvileucalin B-Reference-Cited by-同舟云学术

Enantioselective Total Synthesis of (+)-Salvileucalin B

Published:2010-12-21 Issue:4 Volume:133 Page:774-776
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Levin Sergiy¹,Nani Roger R.¹,Reisman Sarah E.¹

Affiliation:

1. The Warren and Katharine Schlinger Laboratory for Chemistry and Chemical Engineering, Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, California 91125, United States

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja110192b

Reference24 articles.

1. Salvileucalin B, A Novel Diterpenoid with an Unprecedented Rearranged Neoclerodane Skeleton from Salvia leucantha Cav.

2. Salvinorin, a new trans-neoclerodane diterpene from Salvia divinorum(Labiatae)

3. General Methodology for the Topologically Selective Preparation of Linear and Nonlinear Tricyclopentanoids of Hirsutane and Isocomene Typeviaa Claisen Rearrangement / Cyclopentene Annulation Sequence. Total Synthesis of (±)- Epiisocomene

4. Enantioselective Synthesis of Fused Cycloheptadienes by a Tandem Intramolecular Cyclopropanation/Cope Rearrangement Sequence

5. Ligand Effects on the Chemoselectivity of Transition Metal Catalyzed Reactions ofα-Diazo Carbonyl Compounds

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