A model for the stereoselective conjugate addition of lithium (α-methylbenzyl) benzylamide, to t-butyl cinnamate has been devised, using molecular modelling techniques. © 1994
Enantiopure ε-O-silyloxy- and ε-O-benzyloxy-α,β-unsaturated esters derived from d-ribose, each conta...
The doubly diastereoselective conjugate addition of the antipodes of lithium N-benzyl-N-(alpha-methy...
The doubly diastereoselective conjugate addition of the antipodes of lithium N-benzyl-N-(alpha-methy...
A model for the stereoselective conjugate addition of lithium (α-methylbenzyl) benzylamide, to t-but...
A model for the stereoselective conjugate addition of lithium (α-methylbenzyl) benzylamide, to t-but...
"Matching" and "mismatching" effects in the doubly diastereoselective conjugate additions of the ant...
As part of a long-term goal directed towards the ab initio asymmetric synthesis of unnatural amino s...
Michael addition of the lithium amide derived from R-N-(α-methylbenzyl)benzylamine to benzyl E-croto...
Upon treatment with homochiral lithium (R)-N-benzyl-N-(α-methylbenzyl)amide, γ-benzyloxy but-2-enoat...
As part of a long-term goal directed towards the ab initio asymmetric synthesis of unnatural amino s...
Upon treatment with homochiral lithium (R)-N-benzyl-N-(alpha-methylbenzyl) amide, gamma-benzyloxy bu...
Upon treatment with homochiral lithium (R)-N-benzyl-N-(alpha-methylbenzyl) amide, gamma-benzyloxy bu...
Conjugate addition of lithium N-allyl-N-α-methylbenzylamide to chiral α,β-unsaturated esters is subj...
Conjugate addition of lithium N-allyl-N-α-methylbenzylamide to chiral α,β-unsaturated esters is subj...
Enantiopure ε-O-silyloxy- and ε-O-benzyloxy-α,β-unsaturated esters derived from d-ribose, each conta...
Enantiopure ε-O-silyloxy- and ε-O-benzyloxy-α,β-unsaturated esters derived from d-ribose, each conta...
The doubly diastereoselective conjugate addition of the antipodes of lithium N-benzyl-N-(alpha-methy...
The doubly diastereoselective conjugate addition of the antipodes of lithium N-benzyl-N-(alpha-methy...
A model for the stereoselective conjugate addition of lithium (α-methylbenzyl) benzylamide, to t-but...
A model for the stereoselective conjugate addition of lithium (α-methylbenzyl) benzylamide, to t-but...
"Matching" and "mismatching" effects in the doubly diastereoselective conjugate additions of the ant...
As part of a long-term goal directed towards the ab initio asymmetric synthesis of unnatural amino s...
Michael addition of the lithium amide derived from R-N-(α-methylbenzyl)benzylamine to benzyl E-croto...
Upon treatment with homochiral lithium (R)-N-benzyl-N-(α-methylbenzyl)amide, γ-benzyloxy but-2-enoat...
As part of a long-term goal directed towards the ab initio asymmetric synthesis of unnatural amino s...
Upon treatment with homochiral lithium (R)-N-benzyl-N-(alpha-methylbenzyl) amide, gamma-benzyloxy bu...
Upon treatment with homochiral lithium (R)-N-benzyl-N-(alpha-methylbenzyl) amide, gamma-benzyloxy bu...
Conjugate addition of lithium N-allyl-N-α-methylbenzylamide to chiral α,β-unsaturated esters is subj...
Conjugate addition of lithium N-allyl-N-α-methylbenzylamide to chiral α,β-unsaturated esters is subj...
Enantiopure ε-O-silyloxy- and ε-O-benzyloxy-α,β-unsaturated esters derived from d-ribose, each conta...
Enantiopure ε-O-silyloxy- and ε-O-benzyloxy-α,β-unsaturated esters derived from d-ribose, each conta...
The doubly diastereoselective conjugate addition of the antipodes of lithium N-benzyl-N-(alpha-methy...
The doubly diastereoselective conjugate addition of the antipodes of lithium N-benzyl-N-(alpha-methy...
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