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Modern methods in stereoselective aldol reactions

Record Type:	Language materials, printed : Monograph/item
Title/Author:	Modern methods in stereoselective aldol reactions/ edited by Rainer Mahrwald.
other author:	Mahrwald, Rainer,
Published:	Weinheim :Wiley-VCH, : c2013.,
Description:	1 online resource :ill. :
Subject:	Aldol condensation. -
Online resource:	http://onlinelibrary.wiley.com/book/10.1002/9783527656714
ISBN:	9783527656714 (electronic bk.)

Modern methods in stereoselective aldol reactions
Modern methods in stereoselective aldol reactions[electronic resource] /edited by Rainer Mahrwald. - Weinheim :Wiley-VCH,c2013. - 1 online resource :ill.

Includes bibliographical references and index.

Stereoselective Acetate Aldol Reactions / Pedro Romea, Fèlix Urpí -- The Vinylogous Mukaiyama Aldol Reaction in Natural Product Synthesis / Martin Cordes, Markus Kalesse -- Organocatalyzed Aldol Reactions / Gabriela Guillena -- Supersilyl Protective Groups in Aldol Reactions / Patrick B Brady, Hisashi Yamamoto -- Asymmetric Induction in Aldol Additions / Luiz C Dias, Ellen C Polo, Emílio C de Lucca, Marco A B Ferreira -- Polypropionate Synthesis via Substrate-Controlled Stereoselective Aldol Couplings of Chiral Fragments / Dale E Ward -- Application of Oxazolidinethiones and Thiazolidinethiones in Aldol Additions / Michael T Crimmins -- Enzyme-Catalyzed Aldol Additions / Pere Clapés, Jesús Joglar.

This sequel to the highly successful and much appreciated ""Modern Aldol Reactions"" continues to provide a systematic overview of methodologies for installing a required configuration during an aldol addition step, but shifts the focus so as to cover the latest developments.As such, it presents a set of brand new tools, including vinylogous Mukaiyama-aldol reactions, substrate-controlled aldol reactions and asymmetric induction in aldol additions. Furthermore, novel developments in existing stereoselective aldol additions are described, such as the deployment of supersilyl groups or organ

ISBN: 9783527656714 (electronic bk.)Subjects--Topical Terms:

898436
Aldol condensation.

LC Class. No.: QD281.C7 / M63 2013

Dewey Class. No.: 547.036

Modern methods in stereoselective aldol reactions
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020 $a 9783527656714 (electronic bk.)
020 $a 3527656715 (electronic bk.)
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020 $a 3527332057 (hbk.)
020 $a 9783527656745 (ePDF)
020 $a 352765674X (ePDF)
020 $a 9783527656738 (ePub)
020 $a 3527656731 (ePub)
020 $a 9783527656721 (mobi)
020 $a 3527656723 (mobi)
020 $a 9781299402140 (MyiLibrary)
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050 4 $a QD281.C7 $b M63 2013
082 0 4 $a 547.036 $2 23
245 0 0 $a Modern methods in stereoselective aldol reactions $h [electronic resource] / $c edited by Rainer Mahrwald.
260 $a Weinheim : $b Wiley-VCH, $c c2013.
300 $a 1 online resource : $b ill.
504 $a Includes bibliographical references and index.
505 0 $a Stereoselective Acetate Aldol Reactions / Pedro Romea, Fèlix Urpí -- The Vinylogous Mukaiyama Aldol Reaction in Natural Product Synthesis / Martin Cordes, Markus Kalesse -- Organocatalyzed Aldol Reactions / Gabriela Guillena -- Supersilyl Protective Groups in Aldol Reactions / Patrick B Brady, Hisashi Yamamoto -- Asymmetric Induction in Aldol Additions / Luiz C Dias, Ellen C Polo, Emílio C de Lucca, Marco A B Ferreira -- Polypropionate Synthesis via Substrate-Controlled Stereoselective Aldol Couplings of Chiral Fragments / Dale E Ward -- Application of Oxazolidinethiones and Thiazolidinethiones in Aldol Additions / Michael T Crimmins -- Enzyme-Catalyzed Aldol Additions / Pere Clapés, Jesús Joglar.
520 $a This sequel to the highly successful and much appreciated ""Modern Aldol Reactions"" continues to provide a systematic overview of methodologies for installing a required configuration during an aldol addition step, but shifts the focus so as to cover the latest developments.As such, it presents a set of brand new tools, including vinylogous Mukaiyama-aldol reactions, substrate-controlled aldol reactions and asymmetric induction in aldol additions. Furthermore, novel developments in existing stereoselective aldol additions are described, such as the deployment of supersilyl groups or organ
588 $a Description based on print version record.
650 0 $a Aldol condensation. $3 898436
650 0 $a Aldehydes. $3 999727
700 1 $a Mahrwald, Rainer, $d 1950- $3 999726
856 4 0 $u http://onlinelibrary.wiley.com/book/10.1002/9783527656714