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Hans-Jürgen Hansen

Showing results (1-10 of 9) with videos related to

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Organic Letters|October 24, 2003
A novel and highly efficient two-carbon ring expansionGeorg Rüedi, Matthias Nagel, Hans-Jürgen Hansen
Organic Letters|August 28, 2004
Three-carbon ring expansion by cyclopropane insertion: macrocyclic musks from readily available C-12 starting materialsGeorg Rüedi, Matthias Nagel, Hans-Jürgen Hansen
Organic Letters|July 19, 2003
Stereo- and regioselectivity in dynamic gas-phase thermoisomerization (DGPTI): novel route to alpha-campholanic acid and derivativesGeorg Rüedi, Matthias Nagel, Hans-Jürgen Hansen
Journal of the American Chemical Society|June 6, 2002
Stereoselectivity of the benzannulation reaction: efficient central-to-axial chirality transferAndrei V Vorogushin, William D Wulff, Hans-Jürgen Hansen
Tetrahedron|January 31, 2009
Central-to-Axial Chirality Transfer in the Benzannulation Reaction of Optically Pure Fischer Carbene Complexes in the Synthesis of AllocolchicinoidsAndrei V Vorogushin, William D Wulff, Hans-Jürgen Hansen
The Journal of Organic Chemistry|December 6, 2003
Steric vs hydrogen-bonding control of atropisomerization: preparation of either diastereomer of configurationally stable allocolchicinoidsAndrei V Vorogushin, William D Wulff, Hans-Jürgen Hansen
Organic Letters|August 28, 2004
Diradical-promoted (N + 2 - 1) ring expansion: an efficient reaction for the synthesis of macrocyclic ketonesGeorg Rüedi, Matthias A Oberli, Matthias Nagel, et al.
Inorganic Chemistry|October 24, 2001
Synthesis of an o-Carboranyl Derivative of 4-[5-(4-Methyl-1-piperazinyl)-2,5'-bi-1H-benzimidazol-2'-yl]phenolMario Argentini, Deborah F. Dos Santos, Regin Weinreich, et al.
The Journal of Organic Chemistry|July 19, 2003
Diels-Alder reaction-aromatization approach toward functionalized ring C allocolchicinoids. Enantioselective total synthesis of (-)-7S-allocolchicineAndrei V Vorogushin, Alexander V Predeus, William D Wulff, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Organic Letters|October 24, 2003
A novel and highly efficient two-carbon ring expansionGeorg Rüedi, Matthias Nagel, Hans-Jürgen Hansen
Organic Letters|August 28, 2004
Three-carbon ring expansion by cyclopropane insertion: macrocyclic musks from readily available C-12 starting materialsGeorg Rüedi, Matthias Nagel, Hans-Jürgen Hansen
Organic Letters|July 19, 2003
Stereo- and regioselectivity in dynamic gas-phase thermoisomerization (DGPTI): novel route to alpha-campholanic acid and derivativesGeorg Rüedi, Matthias Nagel, Hans-Jürgen Hansen
Journal of the American Chemical Society|June 6, 2002
Stereoselectivity of the benzannulation reaction: efficient central-to-axial chirality transferAndrei V Vorogushin, William D Wulff, Hans-Jürgen Hansen
Tetrahedron|January 31, 2009
Central-to-Axial Chirality Transfer in the Benzannulation Reaction of Optically Pure Fischer Carbene Complexes in the Synthesis of AllocolchicinoidsAndrei V Vorogushin, William D Wulff, Hans-Jürgen Hansen
The Journal of Organic Chemistry|December 6, 2003
Steric vs hydrogen-bonding control of atropisomerization: preparation of either diastereomer of configurationally stable allocolchicinoidsAndrei V Vorogushin, William D Wulff, Hans-Jürgen Hansen
Organic Letters|August 28, 2004
Diradical-promoted (N + 2 - 1) ring expansion: an efficient reaction for the synthesis of macrocyclic ketonesGeorg Rüedi, Matthias A Oberli, Matthias Nagel, et al.
Inorganic Chemistry|October 24, 2001
Synthesis of an o-Carboranyl Derivative of 4-[5-(4-Methyl-1-piperazinyl)-2,5'-bi-1H-benzimidazol-2'-yl]phenolMario Argentini, Deborah F. Dos Santos, Regin Weinreich, et al.
The Journal of Organic Chemistry|July 19, 2003
Diels-Alder reaction-aromatization approach toward functionalized ring C allocolchicinoids. Enantioselective total synthesis of (-)-7S-allocolchicineAndrei V Vorogushin, Alexander V Predeus, William D Wulff, et al.
Pageof 1