Titanocene(III) complexes, easily generated in situ from commercial Ti(IV) precursors, catalyze Barbier-type allylations, intramolecular crotylations (cyclizations), and prenylations of a wide range of aldehydes and ketones. The reaction displays surprising and unprecedented mechanistic subtleties. In cyclizations a fast and irreversible addition of an allyl radical to a Ti(III)-coordinated carbonyl group seems to occur. Intermolecular additions to conjugated aldehydes proceed through a coupling of a Ti(IV)-bound ketyl radical with an allyl radical. Reactions of ketones with allylic halides take place by the classical addition of an allylic organometallic reagent. The radical coupling processes enable transformations such as the highly regioselective alpha-prenylation that are otherwise difficult to achieve. The mild reaction conditions and the possibility to employ titanocene complexes in only catalytic quantities are highly attractive features of our protocol. These unusual properties have been taken advantage of for the straightforward synthesis of the natural products rosiridol, shikalkin, and 12-hydroxysqualene.

Titanocene(III) chemistry has emerged in the last decades as an indispensable tool in C-C bond-forming reactions. In this context, pinacol and related reactions allow the stereoselective synthesis of vicinal diols. In this work, we present new applications of these reactions using as starting materials aromatic ketones. Simple and smooth reaction conditions have been developed and have been applied for inter- and intramolecular processes. We also describe that although Cp(2)TiCl is usually used as a monoelectronic reducing agent, it can be also used as an efficient Lewis acid.

We describe the first Ti-catalyzed Reformatsky-type coupling between alpha-halo ketones and aldehydes. The reaction affords beta-hydroxy ketones under mild, neutral conditions compatible with ketones and other electrophiles. The catalytic cycle possibly proceeds via bis(cyclopentadienyl)titanium enolates.

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From conformational flexibility to rigidity: The straightforward synthesis of rigid molecules with a transannular oxygen bridge starting from flexible germacrolides, which are easily obtained from renewable sources, is described (see scheme). Transannular cyclization of medium‐sized rings enhances molecular rigidity and structural complexity, two properties often associated with biological activity in small molecules.

Alcohols Q 0230Unexpected Ti III /Mn-Promoted Pinacol Coupling of Ketones. -A number of aromatic ketones as well as unsaturated ketones can be used as substrates. Inter-and intramolecular reactions are possible. Additionally, it is shown that trapping of the initially formed ketyl radical with α,β-unsaturated esters allows efficient access to lactones likeXIII). -(PARADAS, M.; CAMPANA, A. G.; ESTEVEZ, R. E.; ALVAREZ DE CIENFUEGOS, L.; JIMENEZ, T.; ROBLES, R.; CUERVA*, J. M.; OLTRA, J. E.; J.

A mild, highly regio- and stereoselective method for the crotylation of aldehydes and ketones mediated/catalyzed by titanocene(III) is described. Optimized conditions permit the selective generation of γ-adducts in high yields together with high stereoselectivity, with a predominance of anti stereoisomers.

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