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00000cam a2200000Mu 4500 |
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on1227390979 |
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OCoLC |
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20240909213021.0 |
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m o d |
| 007 |
cr cnu---unuuu |
| 008 |
201219s2020 si o ||| 0 eng d |
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|a EBLCP
|b eng
|c EBLCP
|d YDX
|d EBLCP
|d N$T
|d OCLCF
|d OCLCO
|d K6U
|d OCLCQ
|d OCLCO
|d OCLCL
|d OCLCQ
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|c (S
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|a 1204606889
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|a 9811405093
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|a 9789811405099
|q (electronic bk.)
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|a (OCoLC)1227390979
|z (OCoLC)1204606889
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| 050 |
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4 |
|a QD262
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| 049 |
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|a HCDD
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| 100 |
1 |
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|a Atta-ur-Rahman.
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| 245 |
1 |
0 |
|a Advances in Organic Synthesis
|h [electronic resource].
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| 260 |
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|a Singapore :
|b Bentham Science Publishers,
|c 2020.
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| 300 |
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|a 1 online resource (333 p.).
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| 490 |
1 |
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|a Advances in Organic Synthesis Ser.
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| 500 |
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|a Description based upon print version of record.
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0 |
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|a Cover -- Title -- Copyright -- End User License Agreement -- Contents -- Preface -- List of Contributors -- Remarkable Advances in the Asymmetric Synthesis of Biologically Active Natural Compounds from the Advent of Chiral Auxiliaries -- Gaspar Diaz-Muñoz1,*, Izabel Luzia Miranda1, Suélen Karine Sartori1, Daniele Cristina de Rezende1, Jefferson Viktor Barros de Paula Baeta2, Fernanda Rodrigues Nascimento2 and Marisa Alves Nogueira Diaz2 -- INTRODUCTION -- EVANS' OXAZOLIDINONES -- Asymmetric Aldol Reactions by Using Evans' Oxazolidinones -- Preparation of the Spiroketal Subunit (1)
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| 505 |
8 |
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|a Preparation of the Polyol Glycoside Subunit (2) -- Synthesis of (−)-Cytovaricin -- COREY'S CHIRAL AUXILIARY: (+)-8-PHENYLMENTHOL -- ENDERS' CHIRAL AUXILIARIES -- CHIRAL AUXILIARIES OF YAMADA -- OPPOLZER'S CHIRAL AUXILIARY -- CARBOHYDRATES AS CHIRAL AUXILIARIES -- KUNZ'S AUXILIARIES -- Asymmetric Reaction of Strecker Employing Kunz's Galactosylamine -- Asymmetric Mannich Reaction Employing the Galactosylamine of Kunz -- MEYERS CHIRAL OXAZOLINES -- AMINO ACIDS AS CHIRAL AUXILIARIES -- SCHÖLLKOPF AUXILIARIES -- CONCLUSIONS -- LIST OF ABBREVIATIONS -- CONSENT FOR PUBLICATION -- CONFLICT OF INTEREST
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| 505 |
8 |
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|a CONFLICT OF INTEREST -- ACKNOWLEDGEMENTS -- REFERENCES -- Carbon-Heteroatom Bond Formation for Medium Ring Heterocycles -- Bhaskar Chatterjee1, Prateek Bhamboo2, Dhananjoy Mondal2 and Smritilekha Bera2,* -- INTRODUCTION -- STRUCTURAL EFFECTS -- RINGS WITH HETEROATOMS OTHER THAN O, N, AND S -- SYNTHETIC METHODS -- STRATEGIES FOR C-X BOND FORMATION -- SYNTHESIS OF 7-MEMBERED RINGS -- TRANSITION METAL CATALYZED REACTIONS -- GREEN SYNTHESIS -- NUCLEOPHILIC CYCLIZATION -- REARRANGEMENT REACTIONS -- SYNTHESIS OF 8-MEMBERED RINGS -- TRANSITION METAL CATALYZED REACTIONS -- NUCLEOPHILIC CYCLIZATION
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| 500 |
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|a REARRANGEMENT REACTIONS.
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| 650 |
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0 |
|a Organic compounds
|x Synthesis.
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| 650 |
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7 |
|a Organic compounds
|x Synthesis
|2 fast
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| 776 |
0 |
8 |
|i Print version:
|a Atta-ur-Rahman
|t Advances in Organic Synthesis: Volume 13
|d Singapore : Bentham Science Publishers,c2020
|z 9789811405082
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| 830 |
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0 |
|a Advances in Organic Synthesis Ser.
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| 856 |
4 |
0 |
|u https://ebookcentral.proquest.com/lib/holycrosscollege-ebooks/detail.action?docID=6424222
|y Click for online access
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| 880 |
8 |
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|6 505-00/(S
|a Addition to β-Position of Ynamides -- With Carbon-Boron Bond Formation -- With Carbon-Carbon Bond Formation -- With Carbon-Phosphorus Bond Formation -- With Carbon-Nitrogen Bond Formation -- With Carbon-Silicon Bond Formation -- Radical Process -- Oxidation -- Rearrangement -- Cyclization -- Metal-Free or Lewis Acid Mediated Cyclization -- Gold-Mediated Cyclization -- Copper-Mediated Cyclization -- Palladium-Mediated Cyclization -- Rhodium-Mediated Cyclization -- Cycloaddition -- [2+1] -- [2+2] -- [3+2] -- [4+1] -- [4+2] -- [2+2+2] -- [5+2] -- CONCLUSION -- CONSENT FOR PUBLICATION
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| 880 |
8 |
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|6 505-00/(S
|a ACKNOWLEDGEMENTS -- REFERENCES -- The Chemistry of Ynamide and Its Application in Organic Synthesis -- Siyu Ye1 and Na Wu1,2,* -- INTRODUCTION -- PREPARATIONS OF YNAMIDES -- Dehydrohalogenation -- Alkynyliodonium Salts -- Ullmann Coupling of Amides -- Oxidative Coupling -- Functionalization of Terminal Ynamides -- Strained Cyclic Ynamide -- REACTIONS OF YNAMIDES -- Addition Reaction -- Addition to α-Position of Ynamides -- With Carbon-Halogen Bond Formation -- With Carbon-Oxygen Bond Formation -- With Carbon-Carbon Bond Formation -- With Carbon-Nitrogen Bond Formation
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| 903 |
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|a EBC-AC
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| 994 |
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|a 92
|b HCD
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