東華大學圖書館 |

Language: English

Help

回圖書館首頁

手機版館藏查詢

Back

Switch To: Labeled | MARC Mode | ISBD

Synthetic methods for biologically a...

Brenna, Elisabetta.

Linked to FindBook

Google Book

Amazon

博客來

Synthetic methods for biologically active molecules = exploring the potential of bioreductions /

Record Type:	Electronic resources : Monograph/item
Title/Author:	Synthetic methods for biologically active molecules/ edited by Elisabetta Brenna.
Reminder of title:	exploring the potential of bioreductions /
other author:	Brenna, Elisabetta.
Published:	Weinheim, Germany :Wiley-VCH, : 2014.,
Description:	1 online resource (xviii, 387 p.)
Notes:	Edition statement from running title area.
[NT 15003449]:	Synthetic Methods for Biologically Active Molecules: Exploring the Potential of Bioreductions; Contents; Preface; List of Contributors; 1 Development of Sustainable Biocatalytic Reduction Processes for Organic Chemists; 1.1 Introduction; 1.2 Biocatalytic Reductions of C=O Double Bonds; 1.2.1 Biocatalytic Reductions of Ketones to Alcohols; 1.2.2 Biocatalytic Reductions of Aldehydes to Alcohols; 1.2.3 Biocatalytic Reductions of Carboxylic Acids to Aldehydes; 1.2.4 Biocatalytic Reductions of Carboxylic Acids to Alcohols; 1.3 Biocatalytic Reductions of C=C Double Bonds
[NT 15003449]:	1.4 Biocatalytic Reductions of Imines to Amines1.5 Biocatalytic Reductions of Nitriles to Amines; 1.6 Biocatalytic Deoxygenation Reactions; 1.7 Emerging Reductive Biocatalytic Reactions; 1.8 Reaction Engineering for Biocatalytic Reduction Processes; 1.9 Summary and Outlook; References; 2 Reductases: From Natural Diversity to Established Biocatalysis and to Emerging Enzymatic Activities; 2.1 Reductases: Natural Occurrence and Context for Biocatalysis; 2.2 Emerging Cases of Reductases in Biocatalysis; 2.2.1 Motivation: The Quest for Novel Enzymes and Reactivities; 2.2.2 Imine Reductases
Subject:	Reduction (Chemistry) -
Online resource:	http://onlinelibrary.wiley.com/book/10.1002/9783527665785
ISBN:	9783527665785 (electronic bk.)

Synthetic methods for biologically active molecules = exploring the potential of bioreductions /
Synthetic methods for biologically active moleculesexploring the potential of bioreductions /[electronic resource] :edited by Elisabetta Brenna. - 1st ed. - Weinheim, Germany :Wiley-VCH,2014. - 1 online resource (xviii, 387 p.)

Edition statement from running title area.

Includes bibliographical references and index.

Synthetic Methods for Biologically Active Molecules: Exploring the Potential of Bioreductions; Contents; Preface; List of Contributors; 1 Development of Sustainable Biocatalytic Reduction Processes for Organic Chemists; 1.1 Introduction; 1.2 Biocatalytic Reductions of C=O Double Bonds; 1.2.1 Biocatalytic Reductions of Ketones to Alcohols; 1.2.2 Biocatalytic Reductions of Aldehydes to Alcohols; 1.2.3 Biocatalytic Reductions of Carboxylic Acids to Aldehydes; 1.2.4 Biocatalytic Reductions of Carboxylic Acids to Alcohols; 1.3 Biocatalytic Reductions of C=C Double Bonds

This ready reference focuses on the currently available toolbox of biocatalysed reductions of C=O, C=C and formal C=N double bonds to show which transformations are reliable for use in manufacturing processes and which still require improvements and investigation.Following an introductory chapter, chapters 2-4 present the synthetic strategies which are currently available for the reduction of C=C, C=O and for reductive amination, by means of whole cell catalysts and isolated enzymes. Chapters 5-7 go on to describe the improvements achieved thus far, illustrating the versatility that is cur

ISBN: 9783527665785 (electronic bk.)Subjects--Topical Terms:

922319
Reduction (Chemistry)

LC Class. No.: QD461

Dewey Class. No.: 548.478

Synthetic methods for biologically active molecules = exploring the potential of bioreductions /
LDR:02863cmm a2200313Ia 4500 001 1953242
003 OCoLC
006 m o d
007 cr |||||||||||
008 150109s2013 gw ob 001 0 eng d
020 $a 9783527665785 (electronic bk.)
020 $a 3527665781 (electronic bk.)
020 $a 9783527665815
020 $a 3527665811
020 $z 9783527333875
035 $a ocn857365390
040 $a EBLCP $b eng $c EBLCP $d IDEBK $d CUS $d MHW
050 4 $a QD461
082 0 4 $a 548.478
245 0 0 $a Synthetic methods for biologically active molecules $h [electronic resource] : $b exploring the potential of bioreductions / $c edited by Elisabetta Brenna.
250 $a 1st ed.
260 $a Weinheim, Germany : $b Wiley-VCH, $c 2014.
300 $a 1 online resource (xviii, 387 p.)
500 $a Edition statement from running title area.
504 $a Includes bibliographical references and index.
505 0 $a Synthetic Methods for Biologically Active Molecules: Exploring the Potential of Bioreductions; Contents; Preface; List of Contributors; 1 Development of Sustainable Biocatalytic Reduction Processes for Organic Chemists; 1.1 Introduction; 1.2 Biocatalytic Reductions of C=O Double Bonds; 1.2.1 Biocatalytic Reductions of Ketones to Alcohols; 1.2.2 Biocatalytic Reductions of Aldehydes to Alcohols; 1.2.3 Biocatalytic Reductions of Carboxylic Acids to Aldehydes; 1.2.4 Biocatalytic Reductions of Carboxylic Acids to Alcohols; 1.3 Biocatalytic Reductions of C=C Double Bonds
505 8 $a 1.4 Biocatalytic Reductions of Imines to Amines1.5 Biocatalytic Reductions of Nitriles to Amines; 1.6 Biocatalytic Deoxygenation Reactions; 1.7 Emerging Reductive Biocatalytic Reactions; 1.8 Reaction Engineering for Biocatalytic Reduction Processes; 1.9 Summary and Outlook; References; 2 Reductases: From Natural Diversity to Established Biocatalysis and to Emerging Enzymatic Activities; 2.1 Reductases: Natural Occurrence and Context for Biocatalysis; 2.2 Emerging Cases of Reductases in Biocatalysis; 2.2.1 Motivation: The Quest for Novel Enzymes and Reactivities; 2.2.2 Imine Reductases
520 $a This ready reference focuses on the currently available toolbox of biocatalysed reductions of C=O, C=C and formal C=N double bonds to show which transformations are reliable for use in manufacturing processes and which still require improvements and investigation.Following an introductory chapter, chapters 2-4 present the synthetic strategies which are currently available for the reduction of C=C, C=O and for reductive amination, by means of whole cell catalysts and isolated enzymes. Chapters 5-7 go on to describe the improvements achieved thus far, illustrating the versatility that is cur
588 $a Description based on online resource; title from PDF title page (Wiley, viewed September 24, 2013)
650 0 $a Reduction (Chemistry) $3 922319
650 0 $a Bioactive compounds $x Synthesis. $3 605681
650 0 $a Enzymes $x Biotechnology. $3 685045
650 0 $a Enzymes $x Industrial applications. $3 661807
700 1 $a Brenna, Elisabetta. $3 2084570
856 4 0 $u http://onlinelibrary.wiley.com/book/10.1002/9783527665785