Synthesis of tryptophans by Lewis acid promoted ring-opening of aziridine-2-carboxylates: optimization of protecting group and Lewis acid-Reference-Cited by-同舟云学术

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Synthesis of tryptophans by Lewis acid promoted ring-opening of aziridine-2-carboxylates: optimization of protecting group and Lewis acid

Published:2013-02 Issue:7 Volume:54 Page:618-620
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Tirotta Ilaria,Fifer Nathan L.,Eakins Julia,Hutton Craig A.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference32 articles.

1. Heterocycles in Natural Product Synthesis;Botuha,2011

2. Aziridines and Epoxides in Organic Synthesis;Zhou,2006

3. Aziridines: epoxides’ ugly cousins?

4. Asymmetric Total Syntheses of (−)-Renieramycin M and G and (−)-Jorumycin Using Aziridine as a Lynchpin

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1. Total Synthesis of Tabernanthine and Ibogaline: Rapid Access to Nosyl Tryptamines;European Journal of Organic Chemistry;2024-05-22

2. Total Synthesis of Dynobactin A;Journal of the American Chemical Society;2024-03-01

3. Aziridine synthesis by the addition of biphenyl imines to ethyl diazoacetate;Synthesis of Aziridines and Oxaziridines from Imines;2024

4. Asymmetric Total Syntheses of Mitragynine, Speciogynine, and 7-Hydroxymitragynine;Chemical and Pharmaceutical Bulletin;2022-09-01

5. Transtion-metal-free access to 2-arylphenethylamines through aryldiazonium ion catalyzed ring-opening of aziridines with arenes;Tetrahedron Letters;2022-07

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