Daniel S. La, Ph.D.
Affiliations: | 2001 | Boston College, Newton, MA, United States |
Area:
catalystsGoogle:
"Daniel La"Mean distance: 8.07 | S | N | B | C | P |
Parents
Sign in to add mentor| Amir H. Hoveyda | grad student | 2001 | Boston College | |
| (Enantioselective synthesis through catalytic metathesis.) | ||||
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Publications
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| La DS, Sattely ES, Ford JG, et al. (2001) Catalytic asymmetric ring-opening metathesis/cross metathesis (AROM/CM) reactions. Mechanism and application to enantioselective synthesis of functionalized cyclopentanes. Journal of the American Chemical Society. 123: 7767-78 |
| La DS, Gair Ford J, Sattely ES, et al. (1999) Tandem catalytic asymmetric ring-opening metathesis/cross metathesis [19] Journal of the American Chemical Society. 121: 11603-11604 |
| Zhu SS, Cefalo DR, La DS, et al. (1999) Chiral Mo-binol complexes: Activity, synthesis, and structure. Efficient enantioselective six-membered ring synthesis through catalytic metathesis Journal of the American Chemical Society. 121: 8251-8259 |
| La DS, Alexander JB, Cefalo DR, et al. (1998) Mo-catalyzed asymmetric synthesis of dihydrofurans. Catalytic kinetic resolution and enantioselective desymmetrization through ring-closing metathesis [21] Journal of the American Chemical Society. 120: 9720-9721 |
| Alexander JB, La DS, Cefalo DR, et al. (1998) Catalytic enantioselective ring-closing metathesis by a chiral biphen- Mo complex [14] Journal of the American Chemical Society. 120: 4041-4042 |
| Harrity JPA, La DS, Cefalo DR, et al. (1998) Chromenes through metal-catalyzed reactions of styrenyl ethers. Mechanism and utility in synthesis Journal of the American Chemical Society. 120: 2343-2351 |
| Xu Z, Johannes CW, Houri AF, et al. (1997) Applications of Zr-Catalyzed Carbomagnesation and Mo-Catalyzed Macrocyclic Ring Closing Metathesis in Asymmetric Synthesis. Enantioselective Total Synthesis of Sch 38516 (Fluvirucin B1) Journal of the American Chemical Society. 119: 10302-10316 |
| Xu Z, Johannes CW, La DS, et al. (1997) Synthesis of amino sugars through a highly diastereoselective dipolar cycloaddition. Enantioselective synthesis of the carbohydrate segment of Sch 38516 Tetrahedron. 53: 16377-16390 |