Synthesis and thermolysis of hexacoordinate 1,2-oxaphosphetanides
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference21 articles.
1. A novel synthetic route to isolable pentacoordinate 1,2-oxaphosphetanes and mechanism of their thermolysis, the second step of the Wittig reaction
2. Synthesis, Structure, and Thermolysis of a 3-Methoxycarbonyl-1, 2λ5-oxaphosphetane
3. Synthesis, Structure, and Thermolysis of a 1,5-Dioxa-4.lambda.5-phosphaspiro[3.3]heptane: A Novel Pentacoordinate 1,2-Oxaphosphetane
4. Synthesis and x-ray crystallographic analysis of pentacoordinate 1,2-oxasiletanides, intermediates of the Peterson reaction
5. Synthesis and crystal structure of a pentacoordinate 1,2-oxagermetanide
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2. Synthesis and characterization of a pair of O-fac/O-mer 12-P-6 alkyloxaphosphates with a P–O–C–C four-membered ring;Chemical Science;2019
3. The chemistry and utility of hexafluoroisobutylene (HFIB) and hexafluoroisobutylene oxide (HFIBO);Journal of Fluorine Chemistry;2013-12
4. Unequivocal Experimental Evidence for a Unified Lithium Salt-Free Wittig Reaction Mechanism for All Phosphonium Ylide Types: Reactions with β-Heteroatom-Substituted Aldehydes Are Consistently Selective forcis-Oxaphosphetane-Derived Products;Journal of the American Chemical Society;2012-05-25
5. Wittig Reactions of Aldehydes Bearing a β-Heteroatom Substituent;Investigation of Reactions Involving Pentacoordinate Intermediates;2012
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