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Frank Roschangar
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Chemical biology of epothilones
KC Nicolaou, F Roschangar, D Vourloumis
Angewandte Chemie International Edition 37 (15), 2014-2045, 1998
5331998
Key Green Chemistry research areas from a pharmaceutical manufacturers’ perspective revisited
MC Bryan, PJ Dunn, D Entwistle, F Gallou, SG Koenig, JD Hayler, ...
Green Chemistry 20 (22), 5082-5103, 2018
4622018
Overcoming barriers to green chemistry in the pharmaceutical industry–the Green Aspiration Level™ concept
F Roschangar, RA Sheldon, CH Senanayake
Green Chemistry 17 (2), 752-768, 2015
3832015
Designed Epothilones: Combinatorial Synthesis, Tubulin Assembly Properties, abd Cytotoxic Action against Taxol‐Resistant Tumor Cells
KC Nicolaou, D Vourloumis, T Li, J Pastor, N Winssinger, Y He, ...
Angewandte Chemie International Edition in English 36 (19), 2097-2103, 1997
3351997
The olefin metathesis approach to epothilone A and its analogues
KC Nicolaou, Y He, D Vourloumis, H Vallberg, F Roschangar, F Sarabia, ...
Journal of the American Chemical Society 119 (34), 7960-7973, 1997
3321997
Sustainability challenges in peptide synthesis and purification: from R&D to production
A Isidro-Llobet, MN Kenworthy, S Mukherjee, ME Kopach, K Wegner, ...
The Journal of organic chemistry 84 (8), 4615-4628, 2019
3142019
The first regioselective palladium-catalyzed indolization of 2-bromo-or 2-chloroanilines with internal alkynes: a new approach to 2, 3-disubstituted indoles
M Shen, G Li, BZ Lu, A Hossain, F Roschangar, V Farina, ...
Organic Letters 6 (22), 4129-4132, 2004
1732004
Regioselective palladium-catalyzed arylation of 2-furaldehyde
MS McClure, B Glover, E McSorley, A Millar, MH Osterhout, F Roschangar
Organic Letters 3 (11), 1677-1680, 2001
1712001
Total synthesis of epothilone E and related side-chain modified analogues via a Stille coupling based strategy
KC Nicolaou, NP King, MRV Finlay, Y He, F Roschangar, D Vourloumis, ...
Bioorganic & medicinal chemistry 7 (5), 665-697, 1999
1661999
The eight criteria defining a good chemical manufacturing process
R Dach, JJ Song, F Roschangar, W Samstag, CH Senanayake
Organic Process Research & Development 16 (11), 1697-1706, 2012
1452012
Chemie und Biologie der Epothilone
KC Nicolaou, F Roschangar, D Vourloumis
Angewandte Chemie 110 (15), 2120-2153, 1998
1331998
Total synthesis of epothilone E and analogues with modified side chains through the Stille coupling reaction
KC Nicolaou, Y He, F Roschangar, NP King, D Vourloumis, T Li
Angewandte Chemie International Edition 37 (1‐2), 84-87, 1998
1301998
A deeper shade of green: inspiring sustainable drug manufacturing
F Roschangar, J Colberg, PJ Dunn, F Gallou, JD Hayler, SG Koenig, ...
Green chemistry 19 (1), 281-285, 2017
1112017
Gezielt entworfene Epothilone: kombinatorische Synthese, Induktion der Tubulin‐Polymerisation und cytotoxische Wirkung gegen taxolresistente Tumorzellen
KC Nicolaou, D Vourloumis, T Li, J Pastor, N Winssinger, Y He, ...
Angewandte Chemie 109 (19), 2181-2187, 1997
881997
Practical total synthesis of (+)-camptothecin: the full story
MA Ciufolini, F Roschangar
Tetrahedron 53 (32), 11049-11060, 1997
831997
A unified strategy for the synthesis of phenanthroizidine alkaloids: Preparation of sterically congested pyridines
MA Ciufolini, F Roschangar
Journal of the American Chemical Society 118 (48), 12082-12089, 1996
831996
Inspiring process innovation via an improved green manufacturing metric: iGAL
F Roschangar, Y Zhou, DJC Constable, J Colberg, DP Dickson, PJ Dunn, ...
Green chemistry 20 (10), 2206-2211, 2018
822018
Efficient Asymmetric Synthesis of Structurally Diverse P‐Stereogenic Phosphinamides for Catalyst Design
ZS Han, L Zhang, Y Xu, JD Sieber, MA Marsini, Z Li, JT Reeves, ...
Angewandte Chemie 127 (18), 5564-5567, 2015
802015
Total Synthesis of Oxazole‐and Cyclopropane‐Containing Epothilone A Analogues by the Olefin Metathesis Approach
KC Nicolaou, H Vallberg, NP King, F Roschangar, Y He, D Vourloumis, ...
Chemistry–A European Journal 3 (12), 1957-1970, 1997
781997
Quinazoline ditosylate salt compounds
MS McClure, MH Osterhout, F Roschangar, MJ Sacchetti
US Patent 7,157,466, 2007
732007
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