Abstract
Reaction of phosphite with silyl enol ethers using iodosobenzene/boron trifluoride etherate provides a direct route for the preparation of 2-aryl-2-oxoalkylphosphonates in good yields.
Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 24, 1994 - Issue 5
![Sample our Physical Sciences journals, sign in here to start your FREE access for 14 days]({"type":"image" , "src" : "/sda/110819/TOC-Subject-Sample-2021-Physical-Sciences.jpg"})
Reprints and Corporate Permissions
Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?
To request a reprint or corporate permissions for this article, please click on the relevant link below:
Academic Permissions
Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?
Obtain permissions instantly via Rightslink by clicking on the button below:
If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.
Related Research Data
A New, Total Synthesis of Methylenomycin B Using Organic Sulfur and Phosphorus Reagents
Source:
Georg Thieme Verlag KG
Hypervalent iodine oxidation of silyl enol ethers under Lewis-acid conditions in methanol. A general route to .alpha.-methoxy ketones
Source:
American Chemical Society (ACS)
Phosphororganische Verbindungen, XXXV. PO-aktivierte Verbindungen als Olefinierungsreagentien
Source:
Wiley
Carbon-Carbon Bond Formation Via Hypervalent Iodine Oxidations
Source:
Georg Thieme Verlag KG
Condensation of long-chain α-˚phosphono carboxylates with aldehydes
Source:
American Chemical Society (ACS)
Direct synthesis of Z-unsaturated esters. A useful modification of the horner-emmons olefination.
Source:
Elsevier BV
Synthese de phosphonates β-carbonyles: I. Par voie carbanionique
Source:
Elsevier BV
Horner-wadsworth-emmons reaction: Use of lithium chloride and an amine for base-sensitive compounds
Source:
Elsevier BV
Reaction of diethyl phosphorochloridite with enolates: a general method for synthesis of .beta.-keto phosphonates and .alpha.-phosphono esters through carbon-phosphorus bond formation
Source:
American Chemical Society (ACS)
Regiochemistry of the rearrangement of cyclohexenyl and cyclohexadienyl phosphates to β-keto phosphonates
Source:
American Chemical Society (ACS)
Carbon–carbon bond formation using hypervalent iodine under Lewis acid conditions: 1,4-diarylbutane-1,4-diones
Source:
Royal Society of Chemistry (RSC)
Michaelis-Arbusow- und Perkow-Reaktionen
Source:
Walter de Gruyter GmbH
Regiocontrolled metalation of diethyl β-dialkylaminovinylphosphonates: A new synthesis of substituted β-ketophosphonates
Source:
Elsevier BV
Regiochemistry of vinyl phosphate/.beta.-keto phosphonate rearrangements in functionalized cyclohexanones and decalones
Source:
American Chemical Society (ACS)
Michaelis-Arbuzov rearrangement
Source:
American Chemical Society (ACS)
Reaction of allyltrimethylsilane with an aromatic compound using hypervalent organoiodine compound: A new allylation of aromatic compounds
Source:
Elsevier BV
α-Cuprophosphonates; III. Synthesis of Ethyl Dialkylphosphonopyruvates
Source:
Georg Thieme Verlag KG
The Utility of Phosphonate Carbanions in Olefin Synthesis
Source:
American Chemical Society (ACS)
Synthetic Applications of Phosphoryl‐Stabilized Anions
Source:
John Wiley & Sons, Inc.
Synthesis of β-keto phosphonates from vinyl phosphates via a 1,3-phosphorus migration
Source:
American Chemical Society (ACS)
Linking provided by
