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43838-G1
The Tandem Claisen-Mislow-Evans Rearrangement
During the first year of the funding period several projects have been initiated and important accomplishments have been achieved. These results are essential for starting my independent career as well engaging graduate students in research. With the help of this grant, graduate students have been able to join the project and spend more time in the laboratory. As evidence of effectiveness of the grant in this regard, four publications with graduate students (including first-year graduate students) and postdocs have been published, and two more future publications (in preparation) will acknowledge the support of the ACS PRF grant. The research performed with the support of the PRF grant is an interplay of the development of new synthetic methodology and the total synthesis of natural products. We developed two new variations of the classic sigmatropic rearrangements as a potential solution to the challenge posed by the structure of marine alkaloid pinnatoxin A. The first reaction is a tandem Claisen-Mislow-Evans rearrangement that efficiently formed the quaternary chiral center at the core of the characteristic spiroimine of pinnatoxin A (Scheme 1). However, we were unable to advance the product further toward pinnatoxin A due to undesired stereochemistry in the cuprate substitution of the allylic pentafluoroacetate 3. The tandem Claisen-Mislow-Evans rearrangement will be employed in the synthesis of other natural products containing a cyclohexenol moiety. Scheme 1. This outcome prompted a change of strategy that stimulated the development of the diastereoselective Ireland-Claisen rearrangement of alpha-branched esters through stereoselective enolization. This type of enolization could not be achieved before in acyclic systems by known methods. The stereodefined, tetrasubstituted enolates are potentially useful for a variety of asymmetric transformations. We initially focused our efforts on the Ireland-Claisen rearrangement and its application in the total synthesis of pinnatoxin A and related natural products. We found that the stereoselectivity of enolization of acyclic, alpha-branched chiral esters can be efficiently controlled using chiral lithium amide bases. We employed widely available bis-(1-phenylethyl)amine and Koga amines as the precursor to the chiral lithium amides. We found that amines 5-7 are generally effective and afford good to excellent selectivities with a range of substrates. For example, enolization of ester 8 with amide 7-Li is highly stereoselective, and the configuration of the enolate is controlled by the chirality of the base. Application for the Ireland-Claisen rearrangement of allylic ester 9 gives ester 10 or 11 stereoselectively, with the sense of selectivity once again controlled by the chirality of the base. Using standard methods (LDA etc.), an equimolar mixture of 10 and 11 is produced. Scheme 2. In short, this methodology allows for a rapid build-up of complexity from readily available chiral carboxylic acids and chiral allylic alcohols via esterification and Ireland-Claisen rearrangement forming congested chiral centers which would be difficult to access by known methods. This methodology is highlighted in our synthesis of the spiroimine fragment of pinnatoxins. As shown in Scheme 3, condensation of alcohol 12 and acid 13, prepared easily by standard methods, followed by the Ireland-Claisen rearrangement afforded 15 in high yield and diastereoselectivity, validating our approach. The reaction performed very well giving identical yield when carried out twice on 2.1 g scale. The product was advanced efficiently to dialdehyde 19, which was cyclized by a high-yielding aldol condensation to form the cyclohexene ring of pinnatoxins. Subsequent manipulations revealed that a better protecting group strategy is desireable. Studies toward this goal are currently underway in our laboratory. We have also prepared the BCD-dispiroketal fragment of pinnatoxins, using the opportunity to study the solvent effect on the thermodynamically controlled selectivity of the acid-catalyzed spiroketalization reaction. This study provided sufficient quantity of this building block to advance further towards the target molecule, which will be a central goal for the next year. In conclusion, we the critical support of the ACS PRF fund, we were able to establish a research program in the area of synthetic organic chemistry that combines the development of new synthetic methods and their application in the synthesis of complex natural products. The importance of this support is underscored by the fact that this is a sole source of external funding at the beginning of our program. Scheme 3.
