Tandem addition–cyclization of o-ethynylphenyl isothiocyanates with N nucleophiles; difference of cyclization mode between primary and secondary amines-Reference-Cited by-同舟云学术

Tandem addition–cyclization of o-ethynylphenyl isothiocyanates with N nucleophiles; difference of cyclization mode between primary and secondary amines

Published:2012-02 Issue:7 Volume:53 Page:748-751
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Kaname Mamoru,Sashida Haruki

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference47 articles.

1. This paper constitutes Part 36 in the series ‘Studies on Chalcogen-Containing Heterocycles’, For Part 35: Sashida, H., Kaname, M. Heterocycles in press. doi: 10.3987/COM-11-S(P)43.

2. 19. Thiazinocyanines. Part I. Carbocyanines containing the 2 : 4-benzthiazine nucleus

3. Synthesis of 4(3H)-quinazolinones from derivatives of methyl 2-isothiocyanatobenzoate

4. Synthesis of Derivatives of Pyrrole Using Methyl 2-Isothiocyanatobenzoate

5. Sulfur-containing heterocycles derived by the reaction of hydroxy-amides and Lawesson's reagent

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