Use of sultines in the asymmetric synthesis of polypropionate antibiotics

At low temperature and in the presence of an acid catalyst, SO2 adds to 1,3-dienes equilibrating with the corresponding 3,6-dihydro-1,2-oxathiin-2-oxides (sultines). These compounds are unstable above -60 °C and equilibrate with the more stable 2,5-dihydrothiophene 1,1-dioxides (sulfolenes). The hetero-Diels-Alder additions of SO2 are suprafacial and follow the Alder endo rule. The sultines derived from 1-oxy-substituted and 1,3-dioxy-disubstituted 1,3-dienes cannot be observed at -100 °C but are believed to be formed faster than the corresponding sulfolenes. In the presence of acid catalysts, the 6-oxy-substituted sultines equilibrate with zwitterionic species that react with electron-rich alkenes such as enoxysilanes and allylsilanes, generating β,γ-unsaturated silyl sulfinates that can be desilylated and desulfinylated to generate polypropionate fragments containing up to three contiguous stereogenic centers and an (E)-alkene unit. Alternatively, the silyl sulfinates can be reacted with electrophiles to generate polyfunctional sulfones (one-pot, four-component synthesis of sulfones), or oxidized into sulfonyl chlorides and reacted with amines, then realizing a one-pot, four-component synthesis of polyfunctional sulfonamides. Using enantiomerically enriched dienes such as 1-[(R)- or 1-(S)-phenylethyloxy]-2-methyl-(E,E)-penta-1,3-dien-3-yl isobutyrate, derived from inexpensive (R)- or (S)-1-phenylethanol, enantiomerically enriched stereotriads are obtained in one-pot operations. The latter are ready for further chain elongation. This has permitted the development of expeditious total asymmetric syntheses of important natural products of biological interest such as the baconipyrones, rifamycin S, and apoptolidin

Use of sultines in the asymmetric synthesis of polypropionate antibiotics

At low temperature and in the presence of an acid catalyst, SO2 adds to 1,3-dienes equilibrating with the corresponding 3,6-dihydro-1,2-oxathiin-2-oxides (sultines). These compounds are unstable above -60 degrees C and equilibrate with the more stable 2,5-dihydrothiophene 1,1-dioxides (sulfolenes). The hetero-Diels-Alder additions of SO2 are suprafacial and follow the Alder endo rule. The sultines derived from 1-oxy-substituted and 1,3-dioxy-disubstituted 1,3-dienes cannot be observed at -100 degrees C but are believed to be formed faster than the corresponding sulfolenes. In the presence of acid catalysts, the 6-oxy-substituted sultines equilibrate with zwitterionic species that react with electron-rich alkenes such as enoxysilanes and allylsilanes, generating beta,gamma-unsaturated silyl sulfinates that can be desilylated and desulfinylated to generate polypropionate fragments containing up to three contiguous stereogenic centers and an (E)-alkene unit. Alternatively, the silyl sulfinates can be reacted with electrophiles to generate polyfunctional sulfones (one-pot, four-component synthesis of sulfones), or oxidized into sulfonyl chlorides and reacted with amines, then realizing a one-pot, four-component synthesis of polyfunctional sulfonamides. Using enantiomerically enriched dienes such as 1-[(R)- or 1-(S)-phenylethyloxyl-2-methyl-(E,E)-penta-1,3-dien-3-yl isobutyrate, derived from inexpensive (R)- or (S)-1-phenylethanol, enantiomerically enriched stereotriads are obtained in one-pot operations. The latter are ready for further chain elongation. This has permitted the development of expeditious total asymmetric syntheses of important natural products of biological interest such as the baconipyrones, rifamycin S, and apoptolidin A

New developments on silyl 2-alkenyl sulfinates and their applications to the asymmetric synthesis of polypropionate fragments

Sulphur dioxide reacts with 1-oxydienes generating zwitterions which are quenched by enoxysilanes to form substituted silyl alkenylsulfinates. These intermediates are desilylated with Bu4NF and the resulting sulfinates react with MeI giving the corresponding methyl sulfones. This new SO2 reaction cascade, hetero-Diels-Alder addition of SO2/oxyallylation/alkylation, was expanded to a variety of electrophiles successfully. Several functional sulfones have been synthesized in modest to high yields. A number of chiral Lewis acids have been prepared and applied into this reaction cascade. Two common techniques were employed to analyze the enantiomeric excess in the resulted sulfones: chiral HPLC and chemical shift reagents. No interesting result was obtained. The removal of water in the reaction system indeed made the reaction better but did not lead to any increase in the enantioselectivity. Silyl sulfinate itself was found not to be able to catalyze the reaction. The formation of (E)-product was discovered in some cases. The introduction of another coordinating oxy-substitution into the dienes did not change the reaction. So the asymmetric catalytic version could not be realized. Silyl sulfinates were found to undergo the silicon/palladium transmetallation. This process could be realized by catalysis with either Pd(PPh3)4 or Pd(OAc)2. The driving force is the formation of silyl acetate. When the sulfinyl palladium complex forms, it can undergo either reductive elimination to give allyl sulfones, or elimination of SO2 in the presence of proton source, such as isopropanol or methanol, giving retro-ene products in good yields. The success of the reactions depended on the amount of the ligand, the solvent and the temperature. More ligand, such as triphenylphosphine, and THF as solvent favor the reductive elimination, while less ligand and CH3CN as solvent favor the retro-ene reaction. The reaction mechanism was studied by NMR experiments which afforded the direct proofs for transmetallation reactions. Kinetic studies on the decomposition of simple silyl alkenylsulfinate into retro-ene products indicated that the cleavage of silicon-oxygen bond could be simply realized by isopropanol. CD3CN was found to have an enormous solvent effect. The presence of Pd(II) species made the reaction somehow faster and cleaner. Related with the studies above it was discovered that trialkylsilyl 2-methylprop-2-enesulfinates are good silylation reagents. For TMS and TES sulfinates, the reactivities were the same and led to 100% conversion in a few minutes for all kinds of alcohols. But for TBS sulfinate, the reactivity decreased significantly due to steric hindrance. Silyl sulfinates were also found to undergo silyl exchange with carboxylic anhydride and acetal/ ketal. The synthetic potential of the sequence hetero-Diels-Alder of SO2, quenching of zwitterions intermediate with an enoxysilane, desilylation and retro-ene elimination of SO2 was demonstrated by the synthesis of (βR,4R,5S,6R)-β,2,2,5-tetramethyl-6-{(1R)-1-[(4S,5S)-2,2,5-trimethyl-1,3-dioxan-4-yl]ethyl}-1,3-dioxane-4-ethanol, a known synthetic intermediate in the total, asymmetric synthesis of Rifamycin S

Use of Sultines in the Asymmetric Synthesis of Polypropionate Antibiotics

At low temperature and in the presence of an acid catalyst, SO2 adds to 1,3-dienes equilibrating with the corresponding 3,6-dihydro-1,2-oxathiin-2-oxides (sultines). These compounds are unstable above -60oC and equilibrate with the more stable 2,5-dihydrothiophene 1,1-dioxides (sulfolenes). The hetero-Diels-Alder additions of SO2 are suprafacial and follow the Alder endo rule. The sultines derived from 1-oxy-substituted and 1,3-dioxy-disubstituted 1,3-dienes cannot be observed at -100oC but are believed to be formed faster than the corresponding sulfolenes. In the presence of acid catalysts, the 6-oxy-substituted sultines equilibrate with zwitterionic species that react with electron-rich alkenes such as enoxysilanes and allylsilanes, generating alfa, beta-unsaturated silyl sulfinates that can be desilylated and desulfinylated to generate polypropionate fragments containing up to three contiguous stereogenic centers and an (E)-alkene unit. Alternatively, the silyl sulfinates can be reacted with electrophiles to generate polyfunctinal sulfones (one-pot, four-component synthesis of sulfones), or oxidized into sulfonyl chlorides and reacted with amines, then realizing a one-pot, four-component synthesis of polyfuctional sulfonamides. Using enantiomerically enriched dienes such as 1-[(R)- or 1-(S)-phenylethyloxy]-2-methyl-(E,E)-penta-1,3-dien-3-yl isobutyrate, derived from inexpensive (R)- or (S)-1-phenylethanol, enantiomerically enriched stereotriads are obtained in one-pot operations. The latter are ready for further chain elongation. This has permitted the development of expeditious total asymmetric syntheses of important natural products of biological interest such as the baconipyrones, rifamycin S, and apoptolidin A