Christopher S. Straub, Ph.D.
Affiliations: | 2000 | Emory University, Atlanta, GA |
Area:
synthesis of heterocyclic compoundsGoogle:
"Christopher Straub"Mean distance: 8.92
Parents
Sign in to add mentor| Albert Padwa | grad student | 2000 | Emory | |
| (Rhodium -mediated cyclizations of alpha-diazo carbonyl compounds: The use of diazo imides and acetylenic diazo esters for alkaloid synthesis.) | ||||
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Publications
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| Padwa A, Zou Y, Cheng B, et al. (2014) Intramolecular cycloaddition reactions of furo[3,4-b]indoles for alkaloid synthesis. The Journal of Organic Chemistry. 79: 3173-84 |
| Padwa A, Straub CS. (2010) ChemInform Abstract: Metallocarbenoid-Induced Cyclizations of Acetylenic Diazo Carbonyl Compounds Cheminform. 31: no-no |
| Padwa A, Crawford KR, Straub CS. (2007) Intramolecular cycloaddition reaction of bromo and nitro substituted furanyl amides Arkivoc. 2007: 14-25 |
| Padwa A, Crawford KR, Straub CS, et al. (2006) Halo substituent effects on intramolecular cycloadditions involving furanyl amides. The Journal of Organic Chemistry. 71: 5432-9 |
| Crawford KR, Bur SK, Straub CS, et al. (2003) Intramolecular cyclization reactions of 5-halo- and 5-nitro-substituted furans. Organic Letters. 5: 3337-40 |
| Padwa A, Straub CS. (2003) Synthesis of furo[3,4-c]furans using a rhodium(II)-catalyzed cyclization/Diels-Alder cycloaddition sequence. The Journal of Organic Chemistry. 68: 227-39 |
| Padwa A, Straub CS. (2000) Facile construction of novel polycyclic ring systems using a metallocarbenoid-induced cyclization of acetylenic diazo carbonyl compounds Organic Letters. 2: 2093-5 |
| Padwa A, Brodney MA, Satake K, et al. (1999) Cycloaddition-Rearrangement Sequence of 2-Amido Substituted Furans as a Method of Synthesizing Hexahydroindolinones. The Journal of Organic Chemistry. 64: 4617-4626 |
| Straub CS, Padwa A. (1999) Synthesis of the angiotensin converting enzyme inhibitor (-)-A58365A via an isomünchnone cycloaddition reaction. Organic Letters. 1: 83-5 |
| Padwa A, Sheehan SM, Straub CS. (1999) An isomunchnone-based method for the synthesis of highly substituted 2(1H)-pyridones Journal of Organic Chemistry. 64: 8648-8659 |