Safety-Catch cleavage

Protected protective groups, see Safety-catch cleavage... 

Safety-catch cleavage of allyl ethers, to form hydroxyl groups, 2-3... 

A more recent approach to safety-catch cleavage of resin-bound amides (PS or ArgoGel resin) to their secondary amides 142 was pubUshed by Sci-cinski et al. in 2004 (Scheme 21) using an indole hnker [176]. 

Cobalt carbonyl complexation can be used in conjunction with a propargylic linker as a safety-catch cleavage method, as described by Fiirst et al. [31]. The propargylic functionality itself is stable under acidic conditions. How-... 

The proper choice of a suitable linker is a therefore a key consideration in the design of a solid-phase chemical route. Linkers have to be developed in order to be stable in the presence of reagents and to permit orthogonal cleavage under mild conditions. Often, cleavage conditions dictate the requirements for work-up and purification steps of the released compound. Different cleavage strategies have been developed such as photocleavable, safety catch and traceless linkers as mentioned in Section 3.2.2 [20]. 

The development of sulfone linkers, the exploration of sulfone based chemical transformations and cleavage strategies are an important objective in soHd-phase organic synthesis. This kind of Hnker (Tab. 3.7) has been used with thioethers [108], sulfoxides [109], sulfones [110], sulfonic acids and their corresponding derivatives [111]. Because carbon-sulfur bonds can be cleaved under very mild conditions, some Hnkers have been based on this effect. They can be cleaved under reductive conditions ]112, 113], photolytic conditions [114, 115] or with strong bases [116]. Various safety catch Hnkers have been developed based on the fact that thiols can be oxidized to sulfoxides and sulfones [112, 113]. 

Nowadays, solid-phase synthesis has been used as a powerful tool in organic chemistry, especially to prepare small molecule libraries. New linkers to obtain different functionalities after cleavage have been developed. There are different linkers strategies (Fig. 3.2), for example traceless linkers, multifunctional linkers, safety catch linkers, fragmentation/ cycloreversion cleavage linkers, cyclization cleavage linkers, which are useful methods for combinatorial solid-phase chemistry. 

Waldmann et al. developed a second exo-linker following a new approach [43-44] which makes use of a safety-catch linker. It is based on the enzymatic cleavage of a functional group embodied in the linker. In this way an intermediate is generated, which subsequently cyclizes intramolecularly according to the principle of assisted removal [54—58] and thereby releases the desired target compounds (Scheme 10.11). 

Resin-bound amides generally need to be activated to make them susceptible to saponification under acceptably mild reaction conditions [114] (Table 3.5). Particularly elegant are those linkers that allow this activation to be realized as the final synthetic step before cleavage (safety-catch linkers [115-117]). The activation of some amide-based safety-catch linkers is outlined in Figure 3.9. 

Figure 3.9. Activation and nucleophilic cleavage of amide-based safety-catch linkers [118,119].

Entry 9 in Table 3.13 is an example of a safety-catch linker, which requires activation by TFA-mediated cleavage of a tert-butyl ether. The unactivated 2-(tm-butoxyj-phenyl esters are cleaved by amines 700 times more slowly than the corresponding 2-hydroxyphenyl esters [289]. A similar linker has been described [290], in which a benzyl ether is used instead of a ferf-butyl ether. Activation of this linker by debenzy-lation was achieved by treatment with HF or HBr/TFA [290]. 

Amides are generally very resistant towards nucleophilic cleavage. Safety-catch linkers, such as those described in Section 3.1.2.3, can, however, be cleaved by amines to yield amides (Entries 1 and 2, Table 3.15). Entry 4 in Table 3.15 is an example of a... 

Table 3.26 lists illustrative examples of cleavage reactions of support-bound N-aryl-carbamates, anilides, and /V-arylsulfonamidcs. /V-Arylcarbamatcs are more susceptible to attack by nucleophiles than /V-alkylcarbamates, and, if strong bases or nucleophiles are to be used in a reaction sequence, it might be a better choice to link the aniline to the support as an /V-bcnzyl derivative. Entry 7 (Table 3.26) is an example of a safety-catch linker for anilines, in which activation is achieved by enzymatic hydrolysis of a phenylacetamide to liberate a primary amine, which then cleaves the anilide. 

Multidirectional cleavage strategies,93,97 98 which offer the possibility to liberate several different functional groups or elements of diversity. Safety-catch linker strategies97,99,100 have been of special interest in this context. 

Arylhydrazides can serve as safety-catch linkers for C-terminal carboxylic acids, amides, or esters. Cleavage proceeds via oxidation with copper(II) salts and subsequent cleavage of the diazenyl moiety by means of a nucleophile [39] (Scheme 6.1.8). 

Sulfur has been used in linkers such as thioethers, sulfoxides, sulfones, sulfonic acids and their corresponding derivatives. A safety-catch linker for amines is based on 2-(thiobenzyl)ethylcarbamates [44]. Linkage is performed with preformed handles containing ethenyloxycarbonyl-protected amines 37. Attachment to thiomethyl-ated polystyrene 38 is performed under conditions involving radicals. Cleavage was performed with an oxidizing agent, which forms the retro Michael substrate (Scheme 6.1.11). 

An anchor for traceless linking might also have a safety-catch function or be suitable for multifunctional cleavage. Linker systems enable the introduction of certain atoms or molecule fragments and will play an important role in the development of diverse organic substance libraries. It is important to point out that the final diversity is achieved on cleavage, and not in an additional solution phase re-... 

A concept with attractive perspectives for increased flexibility in the choice of mutually compatible reaction conditions is termed safety catch. Here, particularly robust linkers are in their stable state during synthesis and are labilized by chemical transformation immediately prior to the final cleavage of the substrates. The SCAL linker [20] becomes acid labile only... 

Cbz-protected amines behave like amides—they are no longer nucleophilic, because the nitrogen s lone pair is tied up in conjugation with the carbonyl group. They are resistant to both aqueous acid and aqueous base, but they have, to use the analogy we developed in the last chapter, an Achilles heel or safety catch—the benzyl ester. The same conditions that removed benzyl ethers in Chapter 24 will remove Cbz HBr or hydrogenolysis. cleavage of Cbz (Z) in HBr/AcOH... 

Some SP hnkers are totally stable during the synthetic sequence and only become labile after a process known as activation, which increases the lability of the linker toward well-defined cleavage conditions. These linkers, known as safety-catch (SC) linkers, are very popular and allow the support and release of many different functionahties. Some examples that rely on different methods of activation are collected in Fig. 1.12 (1.27-1.30) and 1.13 (1.31-1.34). 

Figure 12 A solid-phase total synthesis of the antimycobacterial cyclodepsipeptide kaha-lalide A. The synthesis relies on the Kenner safety-catch linker for attachment to the peptide backbone, followed by macrocyclative cleavage of the linear depsipeptide...

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