Complex achiral

Figure 7 CD spectrum of chloroform solution of crushed cholesterol gallstone absorbance is from complexed achiral bilirubin...

Figure 22 Induced CD of complexes, achiral host 40 and chiral sugar guests 41 CD Aext data were obtained from the...

Inoue et al. ( ) found that a porphyrin-Zn alkyl catalyst polymerized methyloxirane to form a polymer having syndio-rich tacticity. The relative population of the triad tacticities suggests that the stereochemistry of the placement of incoming monomer is controlled by the chirality of the terminal and penultimate units in the growing chain. There is no chirality around the Zn-porphyrin complex. Achiral zinc complex forms syndio-rich poly(methyloxirane), while chiral zinc complex, as stated above, forms isotactic-rich poly(methyloxirane). The situation is just the same as that for propylene polymerizations. Achiral vanadium catalyst produces syndiotactic polypropylene, while chiral titanium catalyst produces isotactic polypropylene. 

Starting from meso-complexes (achiral species), benchrotrenic planar chirality can be generated. The differentiation of the enantiotopic substituents on the aromatic ring has been achieved using enzymes or a chiral palladium catalyst. 

Figure 11.46 Aldol reaction of a chiral carbon-14-labeled boron imide enolate of the sultam type with TiCU pre-complexed achiral/chiral aldehydes to give anti-aldols and application to [ C]avermectin 6/a and Bji,...

The achiral triene chain of (a//-rrans-)-3-demethyl-famesic ester as well as its (6-cis-)-isoiner cyclize in the presence of acids to give the decalol derivative with four chirai centres whose relative configuration is well defined (P.A. Stadler, 1957 A. Escherunoser, 1959 W.S. Johnson, 1968, 1976). A monocyclic diene is formed as an intermediate (G. Stork, 1955). With more complicated 1,5-polyenes, such as squalene, oily mixtures of various cycliz-ation products are obtained. The 18,19-glycol of squalene 2,3-oxide, however, cyclized in modest yield with picric acid catalysis to give a complex tetracyclic natural product with nine chiral centres. Picric acid acts as a protic acid of medium strength whose conjugated base is non-nucleophilic. Such acids activate oxygen functions selectively (K.B. Sharpless, 1970). 

A particular point of interest included in these hehcal complexes concerns the chirality. The heUcates obtained from the achiral strands are a racemic mixture of left- and right-handed double heUces (Fig. 34) (202). This special mode of recognition where homochiral supramolecular entities, as a consequence of homochiral self-recognition, result from racemic components is known as optical self-resolution (203). It appears in certain cases from racemic solutions or melts (spontaneous resolution) and is often quoted as one of the possible sources of optical resolution in the biological world. On the other hand, the more commonly found process of heterochiral self-recognition gives rise to a racemic supramolecular assembly of enantio pairs (204). 

Catalytic Asymmetric Hydroboration. The hydroboration of olefins with catecholborane (an achiral hydroborating agent) is cataly2ed by cationic rhodium complexes with enantiomericaHy pure phosphines, eg, [Rh(cod)2]BE4BINAP, where cod is 1,5-cyclooctadiene and BINAP is... 

The chemistry of complexes having achiral ligands is based solely on the geometrical arrangement on titanium. Optically active alcohols are the most favored monodentate ligands. Cyclopentadienyl is also well suited for chiral modification of titanium complexes. 

An achiral reagent cannot distinguish between these two faces. In a complex with a chiral reagent, however, the two (phantom ligand) electron pairs are in different (enantiotopic) environments. The two complexes are therefore diastereomeric and are formed and react at different rates. Two reaction systems that have been used successfully for enantioselective formation of sulfoxides are illustrated below. In the first example, the Ti(0-i-Pr)4-f-BuOOH-diethyl tartrate reagent is chiral by virtue of the presence of the chiral tartrate ester in the reactive complex. With simple aryl methyl sulfides, up to 90% enantiomeric purity of the product is obtained. 

A second method uses sodium periodate (NaI04) as the oxidant in the presence of the readily available protein bovine serum albumin. In this procedure, the sulfide is complexed in the chiral envirorunent of the protein. Although the oxidant is achiral, it encounters the sulfide in a chiral envirorunent in which the two faces of the sulfide are differentiated. 

Spatial and/or coordinative bias can be introduced into a reaction substrate by coupling it to an auxiliary or controller group, which may be achiral or chiral. The use of chiral controller groups is often used to generate enantioselectively the initial stereocenters in a multistep synthetic sequence leading to a stereochemically complex molecule. Some examples of the application of controller groups to achieve stereoselectivity are shown retrosynthetically in Chart 19. 

In 1997 the application of two different chiral ytterbium catalysts, 55 and 56 for the 1,3-dipolar cycloaddition reaction was reported almost simultaneously by two independent research groups [82, 83], In both works it was observed that the achiral Yb(OTf)3 and Sc(OTf)3 salts catalyze the 1,3-dipolar cycloaddition between nitrones 1 and alkenoyloxazolidinones 19 with endo selectivity. In the first study 20 mol% of the Yb(OTf)2-pyridine-bisoxazoline complex 55 was applied as the catalyst for reactions of a number of derivatives of 1 and 19. The reactions led to endo-selective 1,3-dipolar cycloadditions giving products with enantioselectivities of up to 73% ee (Scheme 6.38) [82]. In the other report Kobayashi et al. described a... 

The l ,J -DBFOX/Ph-transition metal aqua complex catalysts should be suitable for the further applications to conjugate addition reactions of carbon nucleophiles [90-92]. What we challenged is the double activation method as a new methodology of catalyzed asymmetric reactions. Therein donor and acceptor molecules are both activated by achiral Lewis amines and chiral Lewis acids, respectively the chiral Lewis acid catalysts used in this reaction are J ,J -DBFOX/Ph-transition metal aqua complexes. 

Fig, 8,9 The calculated model complexes formed between 3-acroloyl-l, 3-oxazolidin-2-one and an achiral analog of TADDOL-TiCl2,... 

As a unichiral additive which is mixed with the racemate of interest to form non-covalent diastereomeric complexes which can be distinguished by achiral techniques. 

The above enantioselectivities are obviously complex functions of many factors, perhaps even more complex than in natural enzymes. Complexity is partly due to the present co-micellar system in which it is difficult to analyze separately the interaction of the substrate with the achiral micelle, and that of the substrate with the catalyst complex. 

In a catalytic asymmetric reaction, a small amount of an enantio-merically pure catalyst, either an enzyme or a synthetic, soluble transition metal complex, is used to produce large quantities of an optically active compound from a precursor that may be chiral or achiral. In recent years, synthetic chemists have developed numerous catalytic asymmetric reaction processes that transform prochiral substrates into chiral products with impressive margins of enantio-selectivity, feats that were once the exclusive domain of enzymes.56 These developments have had an enormous impact on academic and industrial organic synthesis. In the pharmaceutical industry, where there is a great emphasis on the production of enantiomeri-cally pure compounds, effective catalytic asymmetric reactions are particularly valuable because one molecule of an enantiomerically pure catalyst can, in principle, direct the stereoselective formation of millions of chiral product molecules. Such reactions are thus highly productive and economical, and, when applicable, they make the wasteful practice of racemate resolution obsolete. 

The emergence of the powerful Sharpless asymmetric epoxida-tion (SAE) reaction in the 1980s has stimulated major advances in both academic and industrial organic synthesis.14 Through the action of an enantiomerically pure titanium/tartrate complex, a myriad of achiral and chiral allylic alcohols can be epoxidized with exceptional stereoselectivities (see Chapter 19 for a more detailed discussion). Interest in the SAE as a tool for industrial organic synthesis grew substantially after Sharpless et al. discovered that the asymmetric epoxidation process can be conducted with catalytic amounts of the enantiomerically pure titanium/tartrate complex simply by adding molecular sieves to the epoxidation reaction mix-... 

A breakthrough in the area of asymmetric epoxidation came at the beginning of the 1990s, when the groups of Jacobsen and Katsuki more or less simultaneously discovered that chiral Mn-salen complexes (15) catalyzed the enantioselective formation of epoxides [71, 72, 73], The discovery that simple achiral Mn-salen complexes could be used as catalysts for olefin epoxidation had already been made... 

Table 1. l-(Diisopropylaminocarbonyloxy)-2-alkenyl-lithium-TMEDA Complexes by Deprotonation of Achiral or Racemic 2-Alkenyl Diisopropylcarbamates with Butyllithium (Selected Examples)... 

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