Rearrangements Wolff rearrangement

Baker-Venkataraman Rearrangement Beckmann Rearrangement Claisen Rearrangement Curtius Rearrangement Fries Rearrangement Wolff Rearrangement... 

Williamson synthesis Wohl-Ziegler reaction Wolff rearrangement Wolff Kishner reduction Wurtz reaction Wurtz-Fittig reaction... 

The reaction of cyclohexene with the diazopyruvate 25 gives unexpectedly ethyl 3-cyclohexenyl malonate (26), involving Wolff rearrangement. No cyclo-propanation takes place[28]. 1,3-Dipolar cycloaddition takes place by the reaction of acrylonitrile with diazoacetate to afford the oxazole derivative 27[29]. Bis(trimethylstannyl)diazomethane (28) undergoes Pd(0)-catalyzed rearrangement to give the A -stannylcarbodiimide 29 under mild conditions[30]. 

Thiazole acid chlorides react with diazomethane to give the diazoketone. The later reacts with alcoholic hydrogen chloride to give chloroacetylthiazole (Scheme 16). However, the Wolff rearrangement of the diazoketone is not consistently satisfactory (82). Heated with alcohol in the presence of copper oxide the 5-diazomethylketone (24) gives ethyl 5-thiazoleacetate (25) instead of the expected ethoxymethyl 5-thiazolyl ketone (Scheme 17) (83). 

Several ring contraction routes to /3-lactams have been developed. One of the most important is the photochemical Wolff rearrangement of 3-diazopyrrolidine-2,4-diones (178), which provides a general route to 3-carboxyazetidin-2-ones (179). Lack of stereoselectivity is a problem, but facile epimerization is possible because of the electron withdrawing 3-substituent (78T1731). 

Wolff rearrangement, 7, 193 pyrylium salt synthesis from, 3, 871... 

D. Cyclic a-Diazoketones Ring-Contraction in Photolytic Wolff Rearrangements... 

The photolytic decomposition of a-diazoketones, accompanied by rearrangement to ketene (photolytic Wolff rearrangement), has been used successfully in the preparation of A-nor- and C-norsteroids. The method is reviewed in chapter 15 by R. M. Scribner. ... 

Photochemical Wolff rearrangement of 2-diazo-3-ketones, though not widely used as a source of A-norsteroids, is discussed in section V in connection with the mechanism of the important photochemical synthesis of D-norsteroids. Photochemical rearrangement of epoxy ketones is a source of A-nosteroids these rearrangements are discussed in chapter 13. Other photochemical routes to A-norsteroids are known." " ... 

The diazo ketone 3, when treated with silver oxide as catalyst, decomposes into ketocarbene 5 and dinitrogen Na. This decomposition reaction can also be achieved by heating or by irradiation with uv-light. The ketocarbene undergoes a Wolff rearrangement to give a ketene 6 ... 

The intermediacy of a ketocarbene species 4 is generally accepted for the thermal or photochemical Wolff rearrangement oxirenes 8 that are in equilibrium with ketocarbenes, have been identified as intermediates ... 

The Wolff rearrangement is a versatile reaction R can be alkyl as well as aryl most functional groups do not interfere. The generally mild reaction conditions permit an application to sensitive substrates. 

In this section we first discuss photolytic reactions of arenediazonium salts and report on quinone diazides at the end of the section in the context of imaging technology. Diazoalkenes, non-quinonoid diazo ketones, and the Wolff rearrangement are treated in the book on aliphatic diazo compounds (Zollinger, 1995, Chap. 8). 

The photolysis of o-quinone diazides was carefully investigated by Stis in 1944, many years before the development of photoresists. Scheme 10-102 shows the photolysis sequence for the diazoquinone 10.75 formed in the diazotization of 2-amino-1-naphthol. The product of the photolytic step is a ketocarbene (10.76), which undergoes a Wolff rearrangement to a ketene (10.77). In the presence of water in-dene-3-carboxylic acid (10.78) is formed this compound is highly soluble in water and can be removed in the development step. The mechanism given in Scheme 10-102 was not postulated as such by Stis, because in 1944 ketocarbenes were unknown (for a mechanistic discussion of such Wolff rearrangements see review by Zollinger, 1995, Sec. 8.6, and Andraos et al., 1994). 

Wheland intermediate 357 see also Azo coupling reaction, o-complex Wolff rearrangement 80f., 281, 284ff. Woodward-Hoffmann rules 129, 361, 396... 

The rearrangement of acylcarbenes to ketenes is called the Wolff rearrangement (18-8). A few rearrangements in which carbenes rearrange... 

When the Wolff rearrangement is carried out photochemically, the mechanism is basically the same, but another pathway can intervene. Some of the ketocarbene orieinallv formed can undergo a carbene-carbene rearrangement, through an oxi-... 

The diazo ketone can exist in two conformations, called s-(E) and s-(Z). Studies have shown that Wolff rearrangement takes place preferentially from the s-(Z) conformation. 

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