Protection for the Hydroxyl Group, Including 1,2‐ and 1,3‐Diols

Structure and mechanism of a sub-family of enzymes related to N-acetylneuraminate lyase

Conjugated imines and iminium salts as versatile acceptors of nucleophiles

Catalytic asymmetric hydrogenation of quinoline carbocycles: unusual chemoselectivity in the hydrogenation of quinolines

Leading the way: the synthesis of natural products with new biological targets is one of the driving forces for the development of new antibiotics. The synthesis of the two secondary metabolites corallopyronin and myxopyronin have been achieved, which are prominent leads for the inhibition of bacterial RNA polymerase.

The Total Synthesis of Corallopyronin A and Myxopyronin B

/pdf/chloromethoxysilanes-as-protecting-reagents-for-sterically-1omo0lrxzm.pdf

Chloromethoxysilanes as Protecting Reagents for Sterically Hindered Alcohols.

/pdf/reactions-of-1-aza-1-3-butadienes-a-convenient-synthesis-of-4w8ipgqj0k.pdf

Reactions of 1-Aza-1,3-butadienes. A Convenient Synthesis of N-Benzyl-1,4-dihydropyridines.

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Chloromethoxysilanes as Protecting Reagents for Sterically Hindered Alcohols.

Reactions of 1-Aza-1,3-butadienes. A Convenient Synthesis of N-Benzyl-1,4-dihydropyridines.