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Chemistry of thioamides

Murai, Toshiaki.

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Chemistry of thioamides

Record Type:	Electronic resources : Monograph/item
Title/Author:	Chemistry of thioamides/ edited by Toshiaki Murai.
other author:	Murai, Toshiaki.
Published:	Singapore :Springer Singapore : : 2019.,
Description:	vii, 238 p. :ill., digital ;24 cm.
[NT 15003449]:	1. Thioamides : Overview -- 2. Theoretical Aspects of Thioamides -- 3. Synthesis of Thioamides -- 4. Reaction of Thioamides -- 5. Asymmetric Synthesis Using Thioamides -- 6. Synthesis of Heterocycles from Thioamides -- 7.Thioamides-based Transition Metal-complexes -- 8. Thioamide-containing Peptides and Proteins.
Contained By:	Springer eBooks
Subject:	Sulfur. -
Online resource:	https://doi.org/10.1007/978-981-13-7828-7
ISBN:	9789811378287

Chemistry of thioamides
Chemistry of thioamides[electronic resource] /edited by Toshiaki Murai. - Singapore :Springer Singapore :2019. - vii, 238 p. :ill., digital ;24 cm.

1. Thioamides : Overview -- 2. Theoretical Aspects of Thioamides -- 3. Synthesis of Thioamides -- 4. Reaction of Thioamides -- 5. Asymmetric Synthesis Using Thioamides -- 6. Synthesis of Heterocycles from Thioamides -- 7.Thioamides-based Transition Metal-complexes -- 8. Thioamide-containing Peptides and Proteins.

This book covers whole aspects of the sulfur isologues of amides. Starting from the synthetic methods of thioamides, a range of synthetic applications to the construction of carbon-sulfur and carbon-carbon bonds, to asymmetric reactions, to formation of heterocycles are described. Among the array of thiocarbonyl compounds, thioamides are readily handled in room temperature air. Some of their characteristic features are that the polarity of C=S bonds in thioamides is much smaller than C=O bonds in ordinary amides, that thioamides possess higher HOMO and lower LUMO when compared with those of ordinary amides, and that carbon atoms alpha to the C=S and nitrogen atoms in thioamides are more acidic than those in ordinary amides. Theoretical studies further disclose their features. Thioamides are also used as ligands to a wide variety of metals. Their unique photophysical properties and catalytic activities are described here. Characteristic features of biologically relevant thioamides, e.g., thiopeptides and related compounds, are the final focus of the book.

ISBN: 9789811378287

Standard No.: 10.1007/978-981-13-7828-7doiSubjects--Topical Terms:

1027219
Sulfur.

LC Class. No.: QD181.S1 / C446 2019

Dewey Class. No.: 546.723

Chemistry of thioamides
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245 0 0 $a Chemistry of thioamides $h [electronic resource] / $c edited by Toshiaki Murai.
260 $a Singapore : $b Springer Singapore : $b Imprint: Springer, $c 2019.
300 $a vii, 238 p. : $b ill., digital ; $c 24 cm.
505 0 $a 1. Thioamides : Overview -- 2. Theoretical Aspects of Thioamides -- 3. Synthesis of Thioamides -- 4. Reaction of Thioamides -- 5. Asymmetric Synthesis Using Thioamides -- 6. Synthesis of Heterocycles from Thioamides -- 7.Thioamides-based Transition Metal-complexes -- 8. Thioamide-containing Peptides and Proteins.
520 $a This book covers whole aspects of the sulfur isologues of amides. Starting from the synthetic methods of thioamides, a range of synthetic applications to the construction of carbon-sulfur and carbon-carbon bonds, to asymmetric reactions, to formation of heterocycles are described. Among the array of thiocarbonyl compounds, thioamides are readily handled in room temperature air. Some of their characteristic features are that the polarity of C=S bonds in thioamides is much smaller than C=O bonds in ordinary amides, that thioamides possess higher HOMO and lower LUMO when compared with those of ordinary amides, and that carbon atoms alpha to the C=S and nitrogen atoms in thioamides are more acidic than those in ordinary amides. Theoretical studies further disclose their features. Thioamides are also used as ligands to a wide variety of metals. Their unique photophysical properties and catalytic activities are described here. Characteristic features of biologically relevant thioamides, e.g., thiopeptides and related compounds, are the final focus of the book.
650 0 $a Sulfur. $3 1027219
650 0 $a Sulfur compounds. $3 1027211
650 1 4 $a Organic Chemistry. $3 890856
650 2 4 $a Catalysis. $3 560465
700 1 $a Murai, Toshiaki. $3 3410287
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773 0 $t Springer eBooks
856 4 0 $u https://doi.org/10.1007/978-981-13-7828-7
950 $a Chemistry and Materials Science (Springer-11644)