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007 | cr cnu|||unuuu | ||
008 | 130307s2013 enka ob 001 0 eng d | ||
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020 | _a9783527656714 | ||
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020 | _z3527332057 | ||
020 | _z352765674X | ||
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020 | _z9781299402140 | ||
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_a(OCoLC)829279532 _z(OCoLC)837185854 _z(OCoLC)961570972 _z(OCoLC)962651904 |
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037 |
_a471464 _bMIL |
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050 | 4 |
_aQD281.C7 _bM63 2013 |
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072 | 7 |
_aSCI _2eflch |
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072 | 7 |
_aSCI _x013040 _2bisacsh |
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082 | 0 | 4 |
_a547.036 _223 |
049 | _aMAIN | ||
245 | 0 | 0 |
_aModern methods in stereoselective aldol reactions / _cedited by Rainer Mahrwald. |
260 |
_aWeinheim : _bWiley-VCH, _c©2013. |
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300 |
_a1 online resource (xiv, 536 pages) : _billustrations |
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336 |
_atext _btxt _2rdacontent |
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337 |
_acomputer _bc _2rdamedia |
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338 |
_aonline resource _bcr _2rdacarrier |
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588 | 0 | _aPrint version record. | |
520 | _aThis 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. | ||
504 | _aIncludes bibliographical references and index. | ||
505 | 0 | _aStereoselective 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. | |
650 | 0 | _aAldol condensation. | |
650 | 0 | _aAldehydes. | |
650 | 7 |
_aSCIENCE _xChemistry _xOrganic. _2bisacsh |
|
650 | 7 |
_aAldehydes. _2fast _0(OCoLC)fst00804652 |
|
650 | 7 |
_aAldol condensation. _2fast _0(OCoLC)fst00804678 |
|
650 | 7 |
_aAldolreaktion _2gnd _0(DE-588)4324196-7 |
|
650 | 7 |
_aStereoselektive Reaktion _2gnd _0(DE-588)4132164-9 |
|
655 | 4 | _aElectronic books. | |
700 | 1 |
_aMahrwald, Rainer, _d1950- |
|
776 | 0 | 8 |
_iPrint version: _tModern methods in stereoselective aldol reactions. _dWeinheim : Wiley-VCH, ©2013 _z9783527332052 _w(OCoLC)827785572 |
856 | 4 | 0 |
_uhttp://onlinelibrary.wiley.com/book/10.1002/9783527656714 _zWiley Online Library [Free Download only for SUST IP] |
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