Cyclization versus oligomerization of SP- and RP-5′-OH-N4-benzoyl-2′-deoxycytidine-3′-O-(2-thio-4,4-pentamethylene-1,3,2-oxathiaphospholane)s
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference29 articles.
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3. A stereochemical investigation of the hydrolysis of cyclic AMP and the (Sp)-and (Rp)-diastereoisomers of adenosine cyclic 3′:5′-phosphorothioate by bovine heart and baker's-yeast cyclic AMP phosphodiesterases
4. Inhibition of glycogenolysis in isolated rat hepatocytes by the Rp diastereomer of adenosine cyclic 3‘,5‘-phosphorothioate.
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2. Unlocking P(V): Reagents for chiral phosphorothioate synthesis;Science;2018-09-21
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5. Unexpected Loss of Stereoselectivity in Ring-Opening Reaction of 2-Alkoxy-2-Thio-1,3,2-Oxathiaphospholanes With a Pyrophosphate Anion;Chirality;2014-11-18
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