Synthesis, Structural Characterization, and Conformational Bias in Solution of a Sterically Congested Pyrophosphite:1 Experimental and Computational Evidence for Restricted Rotation about an sp3−sp3 P−O Single Bond
Author:
Affiliation:
1. Additives Division Research Department, Ciba Specialty Chemicals Corporation, 540 White Plains Road, P.O. Box 2005, Tarrytown, New York 10591
Publisher
American Chemical Society (ACS)
Subject
Inorganic Chemistry,Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ic001089c
Reference36 articles.
1. Presented in part at the 212th National Meeting of the American Chemical Society, Orlando, FL, Aug 25−29, 1996; Abstract INOR 142.
2. Tetraethyl Pyrophosphite as a Reagent for Peptide Syntheses1
3. 863. Bis-o-phenylene pyrophosphite: a new reagent for peptide synthesis. Part I. The preparation of some o-phenylene pyrophosphites
4. Oxidative Additions of Coordinated Ligands at Unsaturated Molybdenum and Tungsten Diphosphine-Bridged Carbonyl Dimers. 4. Decarbonylation Reactions of [M2(η5-C5H5)2(CO)4{μ-(EtO)2POP(OEt)2}] (M = Mo, W)
5. Reactivity of [Mn2(.mu.-H)2(CO)6(.mu.-tedip)] (tedip = (EtO)2POP(OEt)2) with Group 11 Alkynyl Compounds. X-ray Structures of [Ag2Mn4(.mu.-H)6(CO)12(.mu.-tedip)2] and [AuMn4(.mu.-H)5(CO)12(.mu.-tedip)2]
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