04053cam a2200769Ia 4500 ocn829279532 OCoLC 20171107091919.0 m o d cr cnu|||unuuu 130307s2013 enka ob 001 0 eng d 9783527656714 3527656715 9783527656745 352765674X 9783527656738 3527656731 9783527656721 3527656723 9783527332052 3527332057 352765674X 9783527656738 3527656731 9783527656721 3527656723 9781299402140 1299402143 AU@ 000050718468 AU@ 000053032919 CHBIS 010131840 CHVBK 314711643 DEBBG BV041390113 DEBSZ 431350159 DKDLA 820120-katalog:000651725 NZ1 15340118 (OCoLC)829279532 (OCoLC)837185854 (OCoLC)961570972 (OCoLC)962651904 471464 MIL DG1 eng pn DG1 EBLCP MHW YDXCP COO CDX OCLCO IDEBK N$T IUL E7B NOC HEBIS OCLCO OCLCF OCLCQ DEBSZ OCLCQ MAIN QD281.C7 M63 2013 SCI eflch SCI 013040 bisacsh 547.036 23 Modern methods in stereoselective aldol reactions / edited by Rainer Mahrwald. [electronic resource] Weinheim : Wiley-VCH, ©2013. 1 online resource (xiv, 536 pages) : illustrations text txt rdacontent computer c rdamedia online resource cr rdacarrier 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 organocatalyzed aldol additions. Throughout, all of these methodologies are presented in the context of their deployment in total synthesis of natural products. Print version record. Aldol condensation. Aldehydes. SCIENCE Chemistry Organic. bisacsh Aldehydes. fast (OCoLC)fst00804652 Aldol condensation. fast (OCoLC)fst00804678 Aldolreaktion gnd (DE-588)4324196-7 Stereoselektive Reaktion gnd (DE-588)4132164-9 Electronic books. Mahrwald, Rainer, 1950- Print version: Modern methods in stereoselective aldol reactions. Weinheim : Wiley-VCH, ©2013 9783527332052 (OCoLC)827785572 http://onlinelibrary.wiley.com/book/10.1002/9783527656714 Wiley Online Library ddc BK 206558 206558