Add to ORKGCHAPTER SIX Chapter six describes a lithiation procedure that allows the production of 3-substituted isoindolin-l-ones in high yields in only one step via lithiation of various substituted N-benzyl-MN-dimethylureas with /-BuLi (3.3 mole equivalents) in THF at 0 °C followed by reactions with various electrophiles. The procedure has been proven to be simple, efficient and general.EThOS - Electronic Theses Online ServiceGBUnited Kingdo
Unexpectedly, lithiation of N'-(2-(2-methylphenyl)ethyl)-N,N-dimethylurea with three equivalents of ...
Lithiation of N-[(2-(4-methoxyphenyl)ethyl)]pivalamide at -20 to 0 oC with three mole equivalents of...
Lithiation of N′-(2-methylbenzyl)-N,N-dimethylurea and N-(2-methylbenzyl)pivalamide with two mole eq...
Chapter One: Chapter one describes a historical overview and the practical consideration of lithiat...
Directed lithiation of various substituted benzylamines takes different courses depending on the sub...
Lithiation of N'-benzyl-N,N-dimethylurea and its substituted derivatives with t-BuLi (3.3 equiv) in ...
Directed lithiation and substitution of various N-benzyl pivalamides and various N'-benzyl-N,N-dimet...
Methoxy-substituted and N-methylated benzylamines were reduced to their 1,4-dihydro derivs. using th...
Part 1: A widely used method of preparing organolithium compounds is by the reductive lithiation of ...
Lithiation of N′-phenethyl-N,N-dimethylurea with three equivalents of tert-butyllithium in anhydrous...
Unexpectedly, lithiation of N'-(2-(2-methylphenyl)ethyl)-N,N-dimethylurea with three equivalents of ...
Lithiation of N-[(2-(4-methoxyphenyl)ethyl)]pivalamide at -20 to 0 oC with three mole equivalents of...
Lithiation of N′-(2-methylbenzyl)-N,N-dimethylurea and N-(2-methylbenzyl)pivalamide with two mole eq...
Chapter One: Chapter one describes a historical overview and the practical consideration of lithiat...
Directed lithiation of various substituted benzylamines takes different courses depending on the sub...
Lithiation of N'-benzyl-N,N-dimethylurea and its substituted derivatives with t-BuLi (3.3 equiv) in ...
Directed lithiation and substitution of various N-benzyl pivalamides and various N'-benzyl-N,N-dimet...
Methoxy-substituted and N-methylated benzylamines were reduced to their 1,4-dihydro derivs. using th...
Part 1: A widely used method of preparing organolithium compounds is by the reductive lithiation of ...
Lithiation of N′-phenethyl-N,N-dimethylurea with three equivalents of tert-butyllithium in anhydrous...
Unexpectedly, lithiation of N'-(2-(2-methylphenyl)ethyl)-N,N-dimethylurea with three equivalents of ...
Lithiation of N-[(2-(4-methoxyphenyl)ethyl)]pivalamide at -20 to 0 oC with three mole equivalents of...
Lithiation of N′-(2-methylbenzyl)-N,N-dimethylurea and N-(2-methylbenzyl)pivalamide with two mole eq...