Stereoselectivity of wittig type olefin synthesis using five-membered cyclic phosphonates. preferential formation of cis olefins

Tetrahedron Letters

Volumn 18, Issue 13, 1977, Pages 1141-1144

  Breuer, Eli ^a   Bannet, Dov M ^a  

^a HEBREW UNIVERSITY OF JERUSALEM   (Israel)

Author keywords

[No Author keywords available]

Indexed keywords

2 ARYLETHYNYLCARBOXYLIC ACID ETHYL ESTER; ALKENYLCARBOXYLIC ACID ETHYL ESTER; DRUG ANALYSIS; DRUG IDENTIFICATION; DRUG STRUCTURE; GAS CHROMATOGRAPHY; IN VITRO STUDY; INFRARED SPECTROMETRY; METHODOLOGY; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; THEORETICAL STUDY;

EID: 0017617182     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(01)92853-9     Document Type: Article

References (23)

1. Stereospecific carbonyl olefination with phosphorylids
2. The mechanism of the Horner?Emmons modification of the Wittig reaction
3. Some observations on the Wadsworth?Emmons olefination reaction
4. Kinetic Study of the Wittig Reaction.
5. Rate Studies of Cyclic Phosphinates, Phosphonates and Phosphates.
6. Displacement Reactions of Phosphorus(V) Compounds and Their Pentacoordinate Intermediates
7. Pentacovalent phosphoranes as intermediates in substitutions at phosphorus
8. Reaction of a nitrone with a phosphono-ylide. A novel approach to aziridines
9. Thermal rearrangement of α,β- to β,γ-unsaturated esters. Evidence for a 1,5-hydrogen transfer mechanism
10. A 5-PHOSPHAFULVENE WITTIG REAGENT