Traceless

Dipolar D / 10 -10 Through space spin-spin interaction, axially symmetric traceless tensor... 

P. Blaney, R. Grigg and V. Sridharan, Traceless Solid-Phase Organic Synthesis, Chem Rev 102 2607-2624 2002. 

Chemistry on solid support has gained tremendous importance during the last few years, mainly driven by the needs of the pharmaceutical sciences. Due to the robust and tolerable nature of the available catalysts, metathesis was soon recognized as a useful technique in this context. Three conceptually different, RCM-based strategies are outlined in Fig. 11. In the approach delineated in Fig. 1 la, a polymer-bound diene 353 is subjected to RCM. The desired product 354 is formed with concomitant traceless release from the resin. This strategy is very favorable, since only compounds with the correct functionality will be liberated, while unwanted by-products remain attached to the polymer. However, as the catalyst is captured in this process by the matrix (355), a higher catalyst loading will be required, or ancillary alkenes have to be added to liberate the catalyst. 

The feasibility of multistep natural product total synthesis via solid-phase methodology, and its application to combinatorial chemistry, was first demonstrated by Nicolaou and coworkers in epothilone synthesis and in the generation of an epothilone library [152]. The traceless release of TBS-protected epoC 361 by RCM of resin-bound precursor 360 (Scheme 69) is an early and most prominent example for the strategy outlined in Fig. 11a. 

Scheme 69 Traceless release of epoC derivative 361 from solid support by RCM [152]...

An illustrative example of an alternative strategy (cf Fig. 11c) involving the use of a novel traceless linker is found in the multistep synthesis of 6-epi-dysidiolide (363) and several dysidiolide-derived phosphatase inhibitors by Waldmann and coworkers [153], outlined in Scheme 70. During the synthesis, the growing skeleton of 363 remained attached to a robust dienic linker. After completion of intermediate 362, the terminal olefin in 363 was liberated from the solid support by the final metathesis process with concomitant formation of a polymer-bound cyclopentene 364. Notably, during the synthesis it turned out that polymer-bound intermediate 365a, in contrast to soluble benzoate 365b, produced diene 367 only in low yield. After introduction of an additional linker (cf intermediate 366), diene 367 was released in distinctly improved yield by RCM. 

Scheme 70 Traceless removal of polymer 364 by RCM in the synthesis of 6-epi-dysidiolide (363) [153]...

The strong variation on B and reflects the fact that the EFG is a traceless tensor with positive and negative components. For > 0 and q = 0, the shift Eq is... 

If D is taken as a traceless tensor, Tr(/)) = Da = 0, there remain only two independent components for D (neglecting the three Euler angles for orientation in a general coordinate system). Usually, these are the parameters D and E, for the axial and rhombic contribution to the ZFS ... 

Although D is in general not necessarily traceless,(4.71) holds for the present... 

The trace of D vanishes when dipole coupling between paramagnetic centers determines the ZFS, since dipole interaction is traceless. A typical example is the ZFS of triplets arising from coupled radical pairs, for which SOC is negligible. For transition metal ions in contrast, SOC is the leading contribution to ZFS and the trace of Zl in general has finite values. 

The values of the rhombicity parameters are conventionally limited to the range 0 < EjD < 1/3 without loss of generality. This corresponds to the choice of a proper coordinate system, for which /)zz (in absolute values) is the largest component of the D tensor, and /) is smaller than Dyy. Any value of rhombicity outside the proper interval, obtained from a simulation for instance, can be projected back to 0 < EID < 1/3 by appropriate 90°-rotations of the reference frame, that is, by permutations of the diagonal elements of D. To this end, the set of nonconventional parameters D and EID has to be converted to the components of a traceless 3x3 tensor D using the relationships... 

Traceless linker 60 based on a benzotriazole scaffold was reacted with amines and aldehydes to produce Mannich-type amine products [69]. Final product release was achieved by treatment with Grignard reagents (Scheme 29). 

Cleavage of all the linkers described above provide a functional group (carboxylic acid, amide, amine, etc) at the anchoring position. Silyl-based handles 71,72, and 73 as well as germanium-based handle 74 insert a C-H bond at the anchoring position and are referred to as traceless (Fig. 15) [82-... 

Aryl hydrazide-based linker 79 was developed as a traceless handle that released products under mild oxidative conditions (Scheme 42) [91]. Polymeric bound p-iodophenylhydrazide was subjected to a variety of Pd°-catalyzed coupling reactions (Heck, Suzuki, Sonogashira, and Stille). Oxidation with Cu(OAc)2 in MeOH and pyridine released the final products in 50-96% yield. 

A traceless linker for solid-phase homo- and hetero-Diels-Alder reactions was based upon resin bound quinodimethane precursors... 

Gayo KM, Suto MJ. Traceless linker Oxidative activation and displacement of a sulfur-based linker. Tetrahedron Lett 1997 38 211-214. 

Kroll FEK, Morphy R, Rees D, Gani D. Resin-immobilized benzyl and aryl vinyl sulfones New versatile traceless linkers for solid-phase organic synthesis. Tetrahedron Lett 1997 38 8573-8576. 

Schiemann K, Showalter HDH. Development of polymer-supported benzotriazole as a novel traceless linker for solid-phase organic synthesis. J Org Chem 1999 64 4972 1975. 

Wilson LJ, Klopfenstein SR, Li M. A traceless linker approach to the solid phase synthesis of substituted guanidines utilizing a novel acyl isothiocyanate resin. Tetrahedron Lett 1999 40 3999 -002. 

Plunkett MJ, Ellman JA. A silicon-based linker for traceless solid-phase synthesis. J Org Chem 1995 60 6006-6007. 

Woolard FX, Paetsch J, Ellman JA. A silicon linker for direct loading of aromatic compounds to supports. Traceless synthesis of pyridinc-bascd tricylics. J Org Chem 1997 62 6102-6103. 

Stieber F, Grether U, Waldmann H. An oxidation-labile traceless linker for solid-phase synthesis. Angew Chem, Int Ed 1999 38 1073-1077. 

Craig D, Robson MJ, Shaw SJ. Traceless linkers for solid-phase synthesis. Homo- and hetero Diels-Alder reactions of ortho-quinodimethanes. Synlett 1998 12 1381-1383. 

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