Andrei Vladimirovich Vorogushin
Affiliations: | 2003 | University of Chicago, Chicago, IL |
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"Andrei Vorogushin"Mean distance: 8.48 | S | N | B | C | P |
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Sign in to add mentorWilliam Dean Wulff | grad student | 2003 | Chicago | |
(Regio- and stereoselective approach to allocolchicinoids: Benzannulation and Diels -Alder reactions. Total synthesis of (-)-allocolchicine.) |
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VOROGUSHIN AV, RESHETOVA MD, AKHMEDOV NG, et al. (2010) ChemInform Abstract: Synthesis and Properties of 7,7-Dichloro-3,4-benzobicyclo[4.1.0]heptane, Its Chromium Tricarbonyl Complexes, and Isomeric 7-Chloro-3,4-benzobicyclo[4.1.0]heptanes. Cheminform. 29: no-no |
Vorogushin AV, Wulff WD, Hansen HJ. (2008) Central-to-Axial Chirality Transfer in the Benzannulation Reaction of Optically Pure Fischer Carbene Complexes in the Synthesis of Allocolchicinoids. Tetrahedron. 64: 949-968 |
Vorogushin AV, Wulff WD, Hansen HJ. (2003) Steric vs hydrogen-bonding control of atropisomerization: preparation of either diastereomer of configurationally stable allocolchicinoids. The Journal of Organic Chemistry. 68: 9618-23 |
Vorogushin AV, Predeus AV, Wulff WD, et al. (2003) Diels-Alder reaction-aromatization approach toward functionalized ring C allocolchicinoids. Enantioselective total synthesis of (-)-7S-allocolchicine. The Journal of Organic Chemistry. 68: 5826-31 |
Vorogushin AV, Wulff WD, Hansen HJ. (2002) Stereoselectivity of the benzannulation reaction: efficient central-to-axial chirality transfer. Journal of the American Chemical Society. 124: 6512-3 |
Vorogushin AV, Wulff WD, Hansen HJ. (2001) Convergent synthesis of fully functionalized ring C allocolchicinoids. Benzannulation approach. Organic Letters. 3: 2641-4 |
Pulley SR, Sen S, Vorogushin A, et al. (1999) Diaryl ethers using fischer chromium carbene mediated benzannulation Organic Letters. 1: 1721-1723 |
Vorogushin AV, Reshetova MD, Akhmedov NG, et al. (1998) Synthesis and properties of 7,7-dichloro-3,4-benzobicyclo[4.1.0]heptane, its tricarbonylchromium complexes, and isomeric 7-chloro-3,4-benzobicyclo[4.1.0]heptanes Russian Chemical Bulletin. 47: 699-703 |