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The ring opening of aziridines with organocuprate reagents provides a new entry to amino acids
The proportions of products derived from competing modes of ring-opening of 1,3-di-tert-butylazirid...
The regioselectivity of the addition reaction of MeOH both in the condensed (MeOH/H2SO4) and in the ...
In this critical review, the ring opening of non-activated 2-substituted aziridines via intermediate...
In this critical review, the ring opening of non-activated 2-substituted aziridines via intermediate...
The regiochemical outcome of the ring opening of the activated and unactivated title aziridines was ...
A. Majee acknowledges the financial support from DST-RSF Major Research Project (Ref. № INT/RUS/RSF/...
The regiochemical outcome of the ring opening of aziridines bearing a polar remote functionality was...
A wide variety of aziridines were converted to the corresponding β-haloamines using activated DMF co...
The regiochem. behavior of the pairs of diastereoisomeric activated aziridines deriving from the cyc...
(S)-3-Amino-2-(1-hydroxy-2,2-dimethylprop-1-yl)-quinazolin-4(3H)-one (Q*NH2) was prepared from (L)-t...
(S)-3-Amino-2-(1-hydroxy-2,2-dimethylprop-1-yl)-quinazolin-4(3H)-one (Q*NH2) was prepared from (L)-t...
(S)-3-Amino-2-(1-hydroxy-2,2-dimethylprop-1-yl)-quinazolin-4(3H)-one (Q*NH2) was prepared from (L)-t...
Ring opening of 1-arylmethyl-2-(cyanomethyl)aziridines with HBr afforded 3-(arylmethyl)amino-4-bromo...
Ring opening of 1-arylmethyl-2-(cyanomethyl)aziridines with HBr afforded 3-(arylmethyl)amino-4-bromo...
The ring opening of aziridines with organocuprate reagents provides a new entry to amino acids
The proportions of products derived from competing modes of ring-opening of 1,3-di-tert-butylazirid...
The regioselectivity of the addition reaction of MeOH both in the condensed (MeOH/H2SO4) and in the ...
In this critical review, the ring opening of non-activated 2-substituted aziridines via intermediate...
In this critical review, the ring opening of non-activated 2-substituted aziridines via intermediate...
The regiochemical outcome of the ring opening of the activated and unactivated title aziridines was ...
A. Majee acknowledges the financial support from DST-RSF Major Research Project (Ref. № INT/RUS/RSF/...
The regiochemical outcome of the ring opening of aziridines bearing a polar remote functionality was...
A wide variety of aziridines were converted to the corresponding β-haloamines using activated DMF co...
The regiochem. behavior of the pairs of diastereoisomeric activated aziridines deriving from the cyc...
(S)-3-Amino-2-(1-hydroxy-2,2-dimethylprop-1-yl)-quinazolin-4(3H)-one (Q*NH2) was prepared from (L)-t...
(S)-3-Amino-2-(1-hydroxy-2,2-dimethylprop-1-yl)-quinazolin-4(3H)-one (Q*NH2) was prepared from (L)-t...
(S)-3-Amino-2-(1-hydroxy-2,2-dimethylprop-1-yl)-quinazolin-4(3H)-one (Q*NH2) was prepared from (L)-t...
Ring opening of 1-arylmethyl-2-(cyanomethyl)aziridines with HBr afforded 3-(arylmethyl)amino-4-bromo...
Ring opening of 1-arylmethyl-2-(cyanomethyl)aziridines with HBr afforded 3-(arylmethyl)amino-4-bromo...
The ring opening of aziridines with organocuprate reagents provides a new entry to amino acids
The proportions of products derived from competing modes of ring-opening of 1,3-di-tert-butylazirid...
The regioselectivity of the addition reaction of MeOH both in the condensed (MeOH/H2SO4) and in the ...