Interesting scientific research on Methyl 3-phenylpropionate

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Recently I am researching about DONOR-ACCEPTOR CYCLOPROPANES; DIELS-ALDER REACTIONS; DIASTEREOSELECTIVE SYNTHESIS; THIOCARBONYL COMPOUNDS; DERIVATIVES; CYCLIZATION; RING, Saw an article supported by the JSPS KAKENHIMinistry of Education, Culture, Sports, Science and Technology, Japan (MEXT)Japan Society for the Promotion of ScienceGrants-in-Aid for Scientific Research (KAKENHI) [JP15H05846, JP18H04263]; Platform Project for Supporting Drug Discovery and Life Science Research (Basis for Supporting Innovative Drug Discovery and Life Science Research (BINDS)) from AMED [JP17am0101091]; JSPSMinistry of Education, Culture, Sports, Science and Technology, Japan (MEXT)Japan Society for the Promotion of Science; [17H03972]; [16 K08166]. Published in WILEY-V C H VERLAG GMBH in WEINHEIM ,Authors: Matsumoto, Y; Tsuji, T; Nakatake, D; Yazaki, R; Ohshima, T. The CAS is 103-25-3. Through research, I have a further understanding and discovery of Methyl 3-phenylpropionate. Recommanded Product: Methyl 3-phenylpropionate

The utility of thionoester as a 1,2-dipolarophile for [4+2] cycloaddition with cyclobutanones is described. The [4+2] cycloaddition reaction provided tetrahydrothiopyran, which is found in biologically active natural products, in high yield with high diastereoselectivity by using readily available TiCl4. This synthetic method was applicable to a wide range of thionoesters and cyclobutanones. The ketone and S,O-ketal functionalities of the product could be reduced with excellent diastereoselectivity. Furthermore, the C-O bond was transformed into a C-C bond, affording contiguous tetrasubstituted carbon centers.

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Reference:
Patent; SANOFI; US2011/294788; (2011); A1;,
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