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The efficient syntheses of pyrroloquinoline tri-cyclic analogs are described.
Efficient syntheses of folate receptor (FR) targeting conjugates of the anti-inflammatory, aminopterin hydrazide, are described.
The two best ranked structures were selected and efficient syntheses developed.
Efficient syntheses of folate conjugates of tubulysins and their hydrazides 1a d are described.
This new approach could be useful in the design of more efficient syntheses of natural products.
This new approach should be useful in the design of more efficient syntheses of morphine and its derivatives.
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Their efficient synthesis still poses a major challenge.
An efficient synthesis of 5′-homoaristeromycin has been developed.
The design and efficient synthesis of AApeptides are described.
These findings have, in return, promoted the development of efficient synthesis strategy.
This process offers an easy and efficient synthesis of 1,4-dihydropyridine derivatives in high yields.
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