Phosphonium ylide

The stabilized phosphonium ylide (601) reacts with aromatic aldehydes to give N-phenacylpyrazoles (602) in good yields (73CC7). Ketone semicarbazones and ketazines react with two moles of phosphorus oxychloride-DMF, the Vilsmeier-Haack reagent, with the formation of 4-formylpyrazoles (603 R = H or PhC=CH2) (70JHC25, 70TL4215). 

Phosphonium hexafluorophosphate, benzotriazolyl-N-hydroxytris(dimethylamino)-in peptide synthesis, 5, 728 Phosphonium salts chromene synthesis from, 3, 753 reactions, 1, 531 Phosphonium salts, vinyl-in pyrrole synthesis, 4, 343 Phosphonium ylides in heterocyclic synthesis, 5, 165 Phosphoramide, triethylene-as pharmaceutical, 1, 157 Phosphoramide, triethylenethio-as pharmaceutical, 1, 157 Phosphorane, pentaphenyl-synthesis, 1, 532 Phosphoranes, 1, 527-537 Berry pseudorotation, 1, 529 bonding, 1, 528... 

Alkenes (olefins) from reaction of phosphonium ylides with aldehydes or ketones... 

Previous syntheses of terminal alkynes from aldehydes employed Wittig methodology with phosphonium ylides and phosphonates. 6 7 The DuPont procedure circumvents the use of phosphorus compounds by using lithiated dichloromethane as the source of the terminal carbon. The intermediate lithioalkyne 4 can be quenched with water to provide the terminal alkyne or with various electrophiles, as in the present case, to yield propargylic alcohols, alkynylsilanes, or internal alkynes. Enantioenriched terminal alkynylcarbinols can also be prepared from allylic alcohols by Sharpless epoxidation and subsequent basic elimination of the derived chloro- or bromomethyl epoxide (eq 5). A related method entails Sharpless asymmetric dihydroxylation of an allylic chloride and base treatment of the acetonide derivative.8 In these approaches the product and starting material contain the same number of carbons. 

Arylmethylene-2-thioxo-4-thiazolidinones (34) react with phosphonium ylides to give dihydrofuro[2,3-rl]thiazol-2(3 -ones (35) in refluxing ethyl acetate, while performing the reaction in refluxing toluene led to the pyrone derivative (36) both of these products result from an initial 1,4-addition to the exocyclic double bond <95T11411>. 

Keywords. Phosphonium, Ylide, Diylide, Wittig, Coordination, Reactivity... 

Reaction of Stabilized Phosphonium Ylides with Activated C=C... 

A related preparation of specific stabilized phosphonium yUdes corresponds to the reaction of triarylphosphines with acetylene dicarboxylic esters in presence of fullerene, which affords a cyclopropanyl-fullerene substituted stabilized phosphonium ylide [9] or the corresponding evolution products [10]. 

Since the pioneering work of H. J. Bestmann and coworkers in the 1960s, acylation of phosphonium ylides is a well known process for the preparation of P-ox-ophosphonium yhdes. The classical way (a) using acylating agents such as acyl chlorides and in situ transylidation is still useful (Scheme 4) [16,17]. 

Further, Wasserman and coworkers developed a direct acylation of stabilized phosphonium ylides by carboxylic acids in presence of the EDCI/DMAP (way c). This last method allows the introduction of a-aminoacid structures into the resulting P-oxo phosphorus ylides [19-25],opening the way to the total synthesis of depsipeptide elastase inhibitors [22,24] or cyclic peptidic protease inhibitor EurystatinA [20]. 

The thermolysis of various substituted phosphonium ylides between 600 °C and 900 °C can afford either substituted alkynes [16,25,27] or cyclic dienes [20] by extrusion of PhjPO, or new stabilized ylides by cyclization of the functional groups [27,28]. 

Particularly interesting are the results obtained with the phosphonium ylides including an acyl rest derived from aminoacid if the N-H bond reactivity is blocked by an amide protection, the alkyne formation takes place [25,27], but if the N-H bond is not deactivated, an intramolecular cyclization occurs to give a new stabilized ylide [27,28]. 

It must also be pointed out that the alkyne synthesis through the FVP process can also be extended to bis()5-oxo phosphonium ylides) for the preparation of 1.3-diynes compounds [16]. 

Oxidation is an important preparation process in the phosphonium ylide chemistry, which can be performed with a lot of oxidizing agents [29]. 

D.K. Taylor and co-workers investigated thoroughly a new route to diastere-omerically pure functionalized cyclopropanes utilizing stabilized phosphonium ylides and y-hydroxyenones derived from 1,2-dioxines (Scheme 7) [34-38]. 

In a related work, the same authors present an expeditious synthesis of functionalized dihydronaphtofurans starting from dihydronaphtodioxines and stabilized phosphonium ylides [39]. 

As in the preceding case with molybdenum, the spectroscopic and X-ray crystallographic data suggest that the complexes obtained can be described as organometallic analogs of resonance-stabilized phosphonium ylides [74]. 

However an unexpected new cyclic ruthenium phosphorus ylide half-sandwich complex 42 has been obtained by reaction of 41 with dichloromethane as solvent [79]. The cyclisation involves a C-Cl activation and corresponds to the incorporation of the methylene moiety in the P-C bond and to the ortho-metal-lation of one phenyl of the phosphine. An other novel unusual phosphonium ylide ruthenium complex 43 has also recently been described [80]. 

A novel chiral dissymmetric chelating Hgand, the non-stabiUzed phosphonium ylide of (R)-BINAP 44, allowed in presence of [Rh(cod)Cl]2 the synthesis of a new type of eight-membered metallacycle, the stable rhodium(I) complex 45, interesting for its potential catalytic properties (Scheme 19) [81]. In contrast to the reactions of stabihzed ylides with cyclooctadienyl palladium or platinum complexes (see Scheme 20), the cyclooctadiene is not attacked by the carbanionic center. Notice that the reactions of ester-stabilized phosphonium ylides of BINAP with rhodium(I) (and also with palladium(II)) complexes lead to the formation of the corresponding chelated compounds but this time with an equilibrium be-... 

When the phosphonium ylide 81 is reacted with zinc amide, the corresponding a-zincated phosphorus yUde is formed. Thermally unstable, it evolves almost quantitatively to zincatacyclobutane 82 which in presence of pyridine leads to the formation of the zincataphosphoniaindane 83. In order to explain this unprecedented cyclometallation reaction, a mechanism is proposed involving a low coordinated zinc center. The new product, reacted with benzaldehyde leads to the diphenylallene 84 (Scheme 27) [106-108]. 

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