Stereo- and regiochemistries of the oxidations of 2-methoxy-5-tert-butyl-1,3,2-dioxaphosphorinanes and the cyclic methyl 3',5'-phosphite of thymidine by water/iodine and oxygen/AIBN to P-chiral phosphates. Oxygen-17 NMR assignment of phosphorus configuration to the diastereomeric thymidine cyclic methyl 3',5'-monophosphates-Reference-Cited by-同舟云学术

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Stereo- and regiochemistries of the oxidations of 2-methoxy-5-tert-butyl-1,3,2-dioxaphosphorinanes and the cyclic methyl 3',5'-phosphite of thymidine by water/iodine and oxygen/AIBN to P-chiral phosphates. Oxygen-17 NMR assignment of phosphorus configuration to the diastereomeric thymidine cyclic methyl 3',5'-monophosphates

Published:1989-05 Issue:11 Volume:111 Page:3981-3987
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Bentrude Wesley G.,Sopchik Alan E.,Gajda Tadeusz

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja00193a034

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