This paper discusses a reaction of phosphorylated α-hydroxyallenes with protected or unprotected hydroxy groups involving 5-endo-trig cyclizations. Various electrophilic reagents such as sulfuryl chloride, bromine, benzenesulfenyl and benzeneselenenyl chlorides have been applied. The paper describes the reaction of 1-hydroxyalkyl-1,2-dienephosphonates with electrophiles that produces 2-methoxy-2-oxo-2,5-dihydro-1,2-oxaphospholes due to the participation of the phosphonate neighbouring group in the cyclization. On the other hand, (1E)-alk-1-en-1-yl phosphine oxides were prepared as mixtures with 2,5-dihydro-1,2-oxaphosphol-2-ium halides in a ratio of about 1:2 by chemo-, regio, and stereoselective electrophilic addition to the C 2 -C 3 -double bond in the allene moiety and subsequent concurrent attack of the external (halide anion) and internal (phosphine oxide group) nucleophiles. The paper proposes a possible mechanism that involves cyclization and additional reactions of the phosphorylated α-hydroxyallenes.

Abstract:The paper describes a convenient and efficient method for regioselective synthesis of phosphorylated α-hydroxyallenes using an atom economical [2,3]-sigmatropic rearrangement of intermediate propargyl phosphites or phosphinites. These can be readily prepared via reaction of protected alkynols with dimethyl chlorophosphite or chlorodiphenyl phosphine respectively in the presence of a base.

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The reaction of the 4‐phosphorylated allenecarboxylates with different electrophilic reagents such as sulfuryl chloride, bromine, benzenesulfanyl, and benzeneselanyl chlorides takes place with a 5‐endo‐trig cyclization or 2,3‐addition reaction depending on the kind of the substituents in the phosphoryl group. Treatment of the 4‐(dimethoxyphosphopyl)‐allenoates with electrophiles gives a mixture of 2,5‐dihydro‐1,2‐oxaphospholes and furan‐2(5H)‐ones in the ratio of about 1.7:1 as a result of the neighboring group participation of phosphonate and carboxylate groups in the cyclization. On the other hand, (3E)‐4‐(diphenylphosphoryl)‐alk‐3‐enoates were prepared, in moderate yields, by chemo‐, regio, and stereoselective electrophilic addition to the C2C3‐double bond in the allenoate moiety. A possible mechanism involving cyclization and addition reactions of the 4‐phosphorylated allenecarboxylates was proposed.

Diphenyl 3‐methylhexa‐1,3,4‐trien‐3‐yl phosphine oxide can be readily prepared via an atom‐economical 2,3‐sigmatropic rearrangement of the mediated alkenynyl phosphinite formed in situ by a reaction of 2‐methylhex‐5‐en‐3‐yn‐2‐ol with diphenylchlorophosphine. Electrophilic cyclization reactions of prepared 1‐vinylallenyl phosphine oxide were investigated as it was established that the reactions proceeded with formation of heterocyclic compounds with participation of the allenic and/or 1,3‐dienic part of the vinylallenic system with neighboring group participation of the phosphoryl and/or vinylic group. © 2012 Wiley Periodicals, Inc. Heteroatom Chem 23:345–351, 2012; View this article online at wileyonlinelibrary.com. DOI 10.1002/hc.21023

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This article presents information about omega-3 (n-3) and omega-6 (n-6) polyunsaturated fatty acid (PUFA) contents in a broad range of commercially important fish species available on Bulgarian fish markets. The aim is to raise consumers' awareness and encourage them to eat fish. Fish species from the Black Sea coast have relatively high proportion of n-3 PUFAs, of which more than 80% is by EPA (eicosapentaenoic acid, C 20:5 n-3) and DHA (docosahexaenoic acid, C 22:6 n-3). Extensive epidemiological studies show that fish consumption is inversely associated with the incidence of cardiovascular diseases (CVD),