Diazeniumdiolate Ions as Leaving Groups in Anomeric Displacement Reactions: A Protection−Deprotection Strategy for Ionic Diazeniumdiolates-Reference-Cited by-同舟云学术

Diazeniumdiolate Ions as Leaving Groups in Anomeric Displacement Reactions: A Protection−Deprotection Strategy for Ionic Diazeniumdiolates

Published:2005-09-24 Issue:41 Volume:127 Page:14188-14189
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Showalter Brett M.¹,Reynolds Melissa M.¹,Valdez Carlos A.¹,Saavedra Joseph E.¹,Davies Keith M.¹,Klose John R.¹,Chmurny Gwendolyn N.¹,Citro Michael L.¹,Barchi, Joseph J.¹,Merz Scott I.¹,Meyerhoff Mark E.¹,Keefer Larry K.¹

Affiliation:

1. Chemistry Section, Laboratory of Comparative Carcinogenesis, National Cancer Institute at Frederick, Frederick, Maryland 21702, Department of Chemistry, University of Michigan, Ann Arbor, Michigan 48109, Basic Research Program, SAIC-Frederick, Inc., National Cancer Institute at Frederick, Frederick, Maryland 21702, Department of Chemistry, George Mason University, Fairfax, Virginia 22030, Laboratory of Proteomics and Analytical Technologies, SAIC-Frederick, Inc., National Cancer Institute at Frederick,...

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja054510a

Reference10 articles.

1. S-Nitrosothiol detection

2. Scope and mechanism of carbohydrase action. Stereocomplementary hydrolytic and glucosyl-transferring actions of glucoamylase and glucodextranase with alpha- and beta-D-glucosyl fluoride.

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