A Simple and Stereospecfic Route to 2,6-Disubstituted 4-Hydroxypiperidines. Synthesis of Dendrobate Alkaloid (+)-241D and Formal Synthesis of (−)-Indolizidine 167B-Reference-Cited by-同舟云学术

A Simple and Stereospecfic Route to 2,6-Disubstituted 4-Hydroxypiperidines. Synthesis of Dendrobate Alkaloid (+)-241D and Formal Synthesis of (−)-Indolizidine 167B

Published:2000-07-18 Issue:16 Volume:2 Page:2503-2505
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Ma Dawei¹,Sun Haiying¹

Affiliation:

1. State Key Laboratory of Bioorganic and Natural Products Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Lu, Shanghai 200032, China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol006176n

Reference24 articles.

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2. (a) Rother, A.Phytochemistry1990,29, 1683.

3. The Structure of 10-epi-Lyfoline, a Novel Alkaloid from Heimia montana

4. Alkaloids from a Panamanian Poison Frog, Dendrobates speciosus: Identification of Pumiliotoxin-A and Allo-pumiliotoxin Class Alkaloids, 3,5-Disubstituted Indolizidines, 5-Substituted 8-Methylindolizidines, and a 2-Methyl-6-nonyl-4-hydroxypiperidine

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