A Metal-Free Approach Toward SaturatedN-Propargyl Heterocycles via an Annulation/Decarboxylative Coupling Sequence-Reference-Cited by-同舟云学术

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A Metal-Free Approach Toward SaturatedN-Propargyl Heterocycles via an Annulation/Decarboxylative Coupling Sequence

Published:2015-06-26 Issue:11 Volume:357 Page:2447-2452
ISSN:1615-4150
Container-title:Advanced Synthesis & Catalysis
language:en
Short-container-title:Adv. Synth. Catal.

Author:

Feng Huangdi,Jia Huihui,Sun Zhihua

Publisher

Wiley

Subject

General Chemistry

Reference91 articles.

1. Synthesis of a novel series of 2,3,4-trisubstituted oxazolidines designed by isosteric replacement or rigidification of the structure and cytotoxic evaluation

2. Mefloquine-Oxazolidine Derivatives: A New Class of Anticancer Agents

3. Chemistry and Biology of the Tetrahydroisoquinoline Antitumor Antibiotics

4. Mefloquine–oxazolidine derivatives, derived from mefloquine and arenecarbaldehydes: In vitro activity including against the multidrug-resistant tuberculosis strain T113

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4. Accessing N‐Propargyl Amino Alcohols through Cu(I)‐Catalyzed A ³ ‐Coupling/Annulation and Bi(III)‐Promoted Ring‐Opening;ChemistrySelect;2022-02-17

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