Synthesis of (–)-Indolizidine 167B based on domino hydroformylation/cyclization reactions
Author:
Publisher
Beilstein Institut
Subject
Organic Chemistry
Link
https://www.beilstein-journals.org/bjoc/content/pdf/1860-5397-4-2.pdf
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1. Further classification of skin alkaloids from neotropical poison frogs (dendrobatidae), with a general survey of toxic/noxious substances in the amphibia
2. Occurrence and Biosynthesis of Animal Peptides Containing a d-Amino Acid
3. Alkaloids from Amphibian Skins
4. Synthesis of Indolizidine 167B
5. Epoxide-Initiated Cationic Cyclization of Azides: A Novel Method for the Stereoselective Construction of 5-Hydroxymethyl Azabicyclic Compounds and Application in the Stereo- and Enantioselective Total Synthesis of (+)- and (−)-Indolizidine 167B and 209D
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3. Reductive Alkylation of Tertiary Lactams via Addition of Organocopper (RCu) Reagents to Thioiminium Ions;The Journal of Organic Chemistry;2017-11-02
4. Rh catalyzed multicomponent tandem and one-pot reactions under hydroformylation conditions;Journal of Molecular Catalysis A: Chemical;2015-11
5. Hydroformylation in Natural Product Synthesis;Topics in Current Chemistry;2013
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