Formal Synthesis of (−)-Perhydrohistrionicotoxin via Cyclic Amino Acid Ester−Enolate Claisen Rearrangement and Ring-Closing Metathesis-Reference-Cited by-同舟云学术

Formal Synthesis of (−)-Perhydrohistrionicotoxin via Cyclic Amino Acid Ester−Enolate Claisen Rearrangement and Ring-Closing Metathesis

Published:2005-06-01 Issue:14 Volume:70 Page:5756-5759
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Kim Sanghee¹,Ko Hyojin¹,Lee Taeho¹,Kim Deukjoon¹

Affiliation:

1. College of Pharmacy, Seoul National University, San 56-1, Shilim, Kwanak, Seoul 151-742, Korea, and Natural Products Research Institute, College of Pharmacy, Seoul National University, 28 Yungun, Jongro, Seoul 110-460, Korea pennkim@snu.ac.kr

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo050608w

Reference28 articles.

1. Histrionicotoxins: Roentgen-Ray Analysis of the Novel Allenic and Acetylenic Spiroalkaloids Isolated from a Colombian Frog, Dendrobates histrionicus

2. Thirty Years of Discovering Arthropod Alkaloids in Amphibian Skin

3. A Two-Directional Synthesis of (±)-Perhydrohistrionicotoxin

4. Combining the [2,3] sigmatropic rearrangement and ring-closing metathesis strategies for the synthesis of spirocyclic alkaloids. A short and efficient route to (±)-perhydrohistrionicotoxin

5. Simple total synthesis of (+-)-perhydrohistrionicotoxin

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