Carbon-carbon condensations via oxyphosphoranes from the reaction of hexafluoroacetone with triphenylphosphine and with diphenyl-phosphinite, phenylphosphonite, and phosphite esters. The oxyphosphorane from triphenylphosphine and phenanthrenequinone-Reference-Cited by-同舟云学术

Carbon-carbon condensations via oxyphosphoranes from the reaction of hexafluoroacetone with triphenylphosphine and with diphenyl-phosphinite, phenylphosphonite, and phosphite esters. The oxyphosphorane from triphenylphosphine and phenanthrenequinone

Published:1966-01 Issue:19 Volume:7 Page:2151-2158
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Ramirez Fausto,Smith C.P.,Gulati A.S.,Patwardhan A.V.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference47 articles.

1. Communications- A New Carbon-Carbon Condensation Reaction Induced by Phosphite Esters. Formation of a 2:1 Adduct in the Reduction of Acenaphthenequinone with Trimethyl Phosphite

2. A Cyclic Saturated Pentaalkoxyphosphorane. Diketols Via Oxyphosphoranes

3. Organic Compounds with Pentavalent Phosphorus. VIII.1 Cyclic Unsaturated Oxyphosphoranes from the Reaction of Tertiary Phosphite Esters with o-Quinones and with α-Diketones

4. Cyclic Saturated Oxyphosphoranes and their Hydrolysis to Cyclic Phosphate Esters. the Diastereomeric 2:1 Biacetyl-Trimethyl Phosphite Adducts

5. A new carbon-carbon condensation via cyclic oxyphosphoranes. Tartaric acids from α-ketoesters

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