Of -talaromycin

Spiroketalization, The synthesis of talaromycin B (3) with four chiral centers by cyclization of an acyclic precursor presents stereochemical problems. A solution involves cyclization of a protected (3-hydroxy ketone with only one chiral center.1 Because of thermodynamic considerations (i.e., all substituents being equatorial and the anomeric effect), cyclization of 1 with HgCl2 in CH3CN followed by acetonation results in the desired product (2, 65% yield) with a stereoselectivity of —10 1. Final steps involve conversion of the hydroxymethyl group to ethyl by tosylation and displacement with lithium dimethylcuprate (80% yield) and hydrolysis of the acetonide group. 

In the total synthesis of talaromycin A, silylmethyl radical cyclization serves as a method for the stereoselective introduction of the 1,3-diol unit64. Starting from the corresponding alcohol, silylation, radical cyclization of the (bromomeihyl)dimethylsilyl eLher 4 and subsequent oxidative cleavage gives the desired product in 78% overall yield. 

Finally, a radical cyclization/oxidation protocol was utilized as the final step in the Crimmins synthesis of the natural product (-)-talaromycin A.41 Silylation of allylic alcohol 42 produced 43, which cyclized upon treatment with BusSnH and AIBN to provide 44. Oxidation of the crude residue resulting from the cyclization reaction resulted in the formation of (-)-talaromycin A (45). 

Temporary tethering of radical precursors has found other applications in natural product synthesis. Crimmins and O Mahony utilized a silyl ether temporary eonnection to direct a hydro-hydroxymethylation of enol ether 139 in their synthesis of talaromycin A, 140 [54]. Since talaromycin A is susceptible to acid-catalyzed isomerization to the thermodynamically more stable talaromycin B in which the hydroxymethyl substituent is equatorial, the use of the essentially neutral conditions of a radical cyclization to install the requisite axial hydroxymethyl group would avoid any potential isomerization problems. Formation of enol ether 139 was achieved in five steps from (4R)-4-ethylvalerolac-tone 141. Exposure of 139 to Bu3SnH in benzene at reflux in the presence of AIBN as initiator effected radical cyclization with delivery of the radical to the same face to whieh the ether tether was attached. Tamao oxidation proceeded uneventfully, furnishing the desired natural product (Scheme 10-47). 

Scheme 10-47 Crimmins and O Mahony used a silicon-tethered radical cyclization in a synthesis of talaromycin A.

Use of the (Bromomethyl)dimethylsilyl Ether Group in a Radical Cyclization in the Synthesis of Talaromycin A, 140 [54]... 

Molecule A (called talaromycin B) is a natural product that contains a ketal unit. Molecule B is a derivative of talaromycin B. Suggest an acyclic precursor that can be transformed to B by a simple chemical reaction. Show that reaction and briefly discuss why B could be formed from this precursor. 

The recent example of talaromycins A and B (Fig. 2.40) produced by the tox-icogenic fungus Talaromyces stipitatus illustrate the strategic utilization of sophisticated spectroscopic techniques in structure determination (239). These two toxins were isolated as a mixture and were extremely difficult to resolve. Due to the loss of water in the positive CI-MS, the molecular ions of these diastereomers were detected only by NCI-MS, with deuterium exchange NCI-MS confirming the presence of two exchangeable protons. The coupling connectivities of the individual diastereomers were mapped with a COSY spectrum (Fig. 2.40). The purified compounds were ultimately separated after formation of their phenyl boronic acid esters (Fig. 2.41). 

Fig. 2.41. a COSY spectrum of talaromycin B (39) after purification as phenylboronic acid ester b expansion of the high-field region of the same spectrum. Solid and dashed lines distinguish the two isolated spin systems (239)... 

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