Tosylmethylisocyanide (TosMIC) [3+2] cycloaddition reactions: A facile Van Leusen protocol for the synthesis of the new class of spirooxazolines, spiropyrrolines and Chromeno[3,4-c]pyrrols-Reference-Cited by-同舟云学术

Tosylmethylisocyanide (TosMIC) [3+2] cycloaddition reactions: A facile Van Leusen protocol for the synthesis of the new class of spirooxazolines, spiropyrrolines and Chromeno[3,4-c]pyrrols

Published:2018-12 Issue:49 Volume:74 Page:7058-7067
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Shaabani Ahmad,Sepahvand Heshmatollah,Bazgir Ayoob,Khavasi Hamid Reza

Funder

Iran National Science Foundation

Research Council of Shahid Beheshti University

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference34 articles.

1. Isocyanides in the Synthesis of Nitrogen Heterocycles

2. Chiral N-Fmoc-β-Amino Alkyl Isonitriles Derived from Amino Acids: First Synthesis and Application in 1-Substituted Tetrazole Synthesis

3. Isocyanide based [4+1] cycloaddition reactions: an indispensable tool in multi-component reactions (MCRs)

4. Synthesis of Imidazo[1,2-a] annulated Pyridines, Pyrazines and Pyrimidines by a Novel Three-Component Condensation

5. Parallel synthesis of 3-aminoimidazo[1,2-a]pyridines and pyrazines by a new three-component condensation

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