Advanced Organic Chemistry: Reactions and synthesisPlenum Press, 1990 - Chemistry, Organic |
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Page 776
... Tetrahedron Lett . 28 , 6261 ( 1987 ) . A. Hosomi , M. Sato , and H. Sakurai , Tetrahedron Lett . , 429 ( 1979 ) . 776 REFERENCES نه نن C. d . e . FOR PROBLEMS f . 10 . 11 . E. J. Corey and W. L. Seibel , Tetrahedron Lett . 27 , 905 ...
... Tetrahedron Lett . 28 , 6261 ( 1987 ) . A. Hosomi , M. Sato , and H. Sakurai , Tetrahedron Lett . , 429 ( 1979 ) . 776 REFERENCES نه نن C. d . e . FOR PROBLEMS f . 10 . 11 . E. J. Corey and W. L. Seibel , Tetrahedron Lett . 27 , 905 ...
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... Tetrahedron Lett . , 3391 ( 1974 ) . 16 . B. Chauncy and E. Gellert , Aust . J. Chem . 22 , 993 ( 1969 ) ; R. I. Duclos , Jr. , J. S. Tung , and H. Rapoport , J. Org . Chem . 49 , 5243 ( 1984 ) . 17 . W. G. Miller and C. U. Pittman , Jr ...
... Tetrahedron Lett . , 3391 ( 1974 ) . 16 . B. Chauncy and E. Gellert , Aust . J. Chem . 22 , 993 ( 1969 ) ; R. I. Duclos , Jr. , J. S. Tung , and H. Rapoport , J. Org . Chem . 49 , 5243 ( 1984 ) . 17 . W. G. Miller and C. U. Pittman , Jr ...
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... Tetrahedron Lett . , 3391 ( 1979 ) . E. Piers , R. W. Britton , and W. de Waal , J. Am . Chem . Soc . 93 , 5113 ( 1971 ) ; K. J. Schmalzl and R. N. Mirrington , Tetrahedron Lett . , 3219 ( 1970 ) ; N. Fukamiya , M. Kato , and A ...
... Tetrahedron Lett . , 3391 ( 1979 ) . E. Piers , R. W. Britton , and W. de Waal , J. Am . Chem . Soc . 93 , 5113 ( 1971 ) ; K. J. Schmalzl and R. N. Mirrington , Tetrahedron Lett . , 3219 ( 1970 ) ; N. Fukamiya , M. Kato , and A ...
Contents
Alkylation of Nucleophilic Carbon Enolates and Enamines | 1 |
CONTENTS | 3 |
Polar Addition and Elimination Reactions | 6 |
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acetic acyl adduct alcohols aldehydes alkenes alkyl allylic amines anion aromatic aryl boron bromide C=C H C₂H carbanions carbon carbonyl carbonyl compounds carbonyl group carboxylic acids catalyst CH,O CH₂ CH₂OH CH3 CH CHAPTER 6 CYCLOADDITIONS Chem chiral chloride Claisen rearrangement CO,CH CO₂C₂H CO₂H cyclic cycloaddition reactions Diels-Alder reactions diene dienophile double bond E. J. Corey electron electrophilic ENAMINES enantioselectivity enol ether epoxides esters examples formation FUNCTIONAL GROUPS give Grignard reagents H CH H H H H H,C H,C CH H,C H,C H. C. Brown H₁C H₂ H₂C H₂O halides halogen hydride hydrogen hydroxyl intermediate intramolecular ketones Lewis acid lithium mechanism methyl molecules n-BuLi organoboranes organolithium organometallic oxidation oxygen Ph Ph PhCH₂O proton radical react reaction conditions REACTIONS INVOLVING reactive ring Scheme SECTION solvents step stereochemistry stereoselectivity steric structure Synth synthesis synthetic Tetrahedron Lett THERMAL ELIMINATIONS transition metal UNIMOLECULAR REARRANGEMENTS ylides