| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5228317 | Tetrahedron | 2008 | 4 Pages |
Abstract
Under mild conditions, the reaction of alkylidene, arylidene, and heteroarylidene malonates with tosylhydrazone salts in the presence of catalytic amount of Rh2(OAc)4 and triphenylarsine affords trans-2,3-disubstituted cyclopropane 1,1-dicarboxylic esters in high yields and high diastereoselectivities.
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