The Experts below are selected from a list of 12 Experts worldwide ranked by ideXlab platform
Rachid Baati - One of the best experts on this subject based on the ideXlab platform.
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highly selective three step synthesis of rhein in chloroaluminate molten salt preclusion of the Hayashi Rearrangement
European Journal of Organic Chemistry, 2009Co-Authors: Vanessa Gonnot, Cyril Antheaume, Marc Nicolas, Charles Mioskowski, Rachid BaatiAbstract:An expeditious, three-step synthesis of rhein (2) was optimized starting from bis(N,N-diethyl)-5-methoxybenzene-1,3-dicarboxamide. The key final step, involving deprotection/cyclization of ortho-benzoylbenzoic acid 9 in acidic chloroaluminate molten salts, yielded the desired natural product with high selectivity and good overall yield by precluding the competitive Hayashi Rearrangement.(© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)
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Highly Selective Three‐Step Synthesis of Rhein in Chloroaluminate Molten Salt: Preclusion of the Hayashi Rearrangement
European Journal of Organic Chemistry, 2009Co-Authors: Vanessa Gonnot, Cyril Antheaume, Marc Nicolas, Charles Mioskowski, Rachid BaatiAbstract:An expeditious, three-step synthesis of rhein (2) was optimized starting from bis(N,N-diethyl)-5-methoxybenzene-1,3-dicarboxamide. The key final step, involving deprotection/cyclization of ortho-benzoylbenzoic acid 9 in acidic chloroaluminate molten salts, yielded the desired natural product with high selectivity and good overall yield by precluding the competitive Hayashi Rearrangement.(© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)
Vanessa Gonnot - One of the best experts on this subject based on the ideXlab platform.
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highly selective three step synthesis of rhein in chloroaluminate molten salt preclusion of the Hayashi Rearrangement
European Journal of Organic Chemistry, 2009Co-Authors: Vanessa Gonnot, Cyril Antheaume, Marc Nicolas, Charles Mioskowski, Rachid BaatiAbstract:An expeditious, three-step synthesis of rhein (2) was optimized starting from bis(N,N-diethyl)-5-methoxybenzene-1,3-dicarboxamide. The key final step, involving deprotection/cyclization of ortho-benzoylbenzoic acid 9 in acidic chloroaluminate molten salts, yielded the desired natural product with high selectivity and good overall yield by precluding the competitive Hayashi Rearrangement.(© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)
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Highly Selective Three‐Step Synthesis of Rhein in Chloroaluminate Molten Salt: Preclusion of the Hayashi Rearrangement
European Journal of Organic Chemistry, 2009Co-Authors: Vanessa Gonnot, Cyril Antheaume, Marc Nicolas, Charles Mioskowski, Rachid BaatiAbstract:An expeditious, three-step synthesis of rhein (2) was optimized starting from bis(N,N-diethyl)-5-methoxybenzene-1,3-dicarboxamide. The key final step, involving deprotection/cyclization of ortho-benzoylbenzoic acid 9 in acidic chloroaluminate molten salts, yielded the desired natural product with high selectivity and good overall yield by precluding the competitive Hayashi Rearrangement.(© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)
Cyril Antheaume - One of the best experts on this subject based on the ideXlab platform.
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highly selective three step synthesis of rhein in chloroaluminate molten salt preclusion of the Hayashi Rearrangement
European Journal of Organic Chemistry, 2009Co-Authors: Vanessa Gonnot, Cyril Antheaume, Marc Nicolas, Charles Mioskowski, Rachid BaatiAbstract:An expeditious, three-step synthesis of rhein (2) was optimized starting from bis(N,N-diethyl)-5-methoxybenzene-1,3-dicarboxamide. The key final step, involving deprotection/cyclization of ortho-benzoylbenzoic acid 9 in acidic chloroaluminate molten salts, yielded the desired natural product with high selectivity and good overall yield by precluding the competitive Hayashi Rearrangement.(© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)
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Highly Selective Three‐Step Synthesis of Rhein in Chloroaluminate Molten Salt: Preclusion of the Hayashi Rearrangement
European Journal of Organic Chemistry, 2009Co-Authors: Vanessa Gonnot, Cyril Antheaume, Marc Nicolas, Charles Mioskowski, Rachid BaatiAbstract:An expeditious, three-step synthesis of rhein (2) was optimized starting from bis(N,N-diethyl)-5-methoxybenzene-1,3-dicarboxamide. The key final step, involving deprotection/cyclization of ortho-benzoylbenzoic acid 9 in acidic chloroaluminate molten salts, yielded the desired natural product with high selectivity and good overall yield by precluding the competitive Hayashi Rearrangement.(© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)
Marc Nicolas - One of the best experts on this subject based on the ideXlab platform.
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highly selective three step synthesis of rhein in chloroaluminate molten salt preclusion of the Hayashi Rearrangement
European Journal of Organic Chemistry, 2009Co-Authors: Vanessa Gonnot, Cyril Antheaume, Marc Nicolas, Charles Mioskowski, Rachid BaatiAbstract:An expeditious, three-step synthesis of rhein (2) was optimized starting from bis(N,N-diethyl)-5-methoxybenzene-1,3-dicarboxamide. The key final step, involving deprotection/cyclization of ortho-benzoylbenzoic acid 9 in acidic chloroaluminate molten salts, yielded the desired natural product with high selectivity and good overall yield by precluding the competitive Hayashi Rearrangement.(© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)
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Highly Selective Three‐Step Synthesis of Rhein in Chloroaluminate Molten Salt: Preclusion of the Hayashi Rearrangement
European Journal of Organic Chemistry, 2009Co-Authors: Vanessa Gonnot, Cyril Antheaume, Marc Nicolas, Charles Mioskowski, Rachid BaatiAbstract:An expeditious, three-step synthesis of rhein (2) was optimized starting from bis(N,N-diethyl)-5-methoxybenzene-1,3-dicarboxamide. The key final step, involving deprotection/cyclization of ortho-benzoylbenzoic acid 9 in acidic chloroaluminate molten salts, yielded the desired natural product with high selectivity and good overall yield by precluding the competitive Hayashi Rearrangement.(© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)
Charles Mioskowski - One of the best experts on this subject based on the ideXlab platform.
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highly selective three step synthesis of rhein in chloroaluminate molten salt preclusion of the Hayashi Rearrangement
European Journal of Organic Chemistry, 2009Co-Authors: Vanessa Gonnot, Cyril Antheaume, Marc Nicolas, Charles Mioskowski, Rachid BaatiAbstract:An expeditious, three-step synthesis of rhein (2) was optimized starting from bis(N,N-diethyl)-5-methoxybenzene-1,3-dicarboxamide. The key final step, involving deprotection/cyclization of ortho-benzoylbenzoic acid 9 in acidic chloroaluminate molten salts, yielded the desired natural product with high selectivity and good overall yield by precluding the competitive Hayashi Rearrangement.(© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)
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Highly Selective Three‐Step Synthesis of Rhein in Chloroaluminate Molten Salt: Preclusion of the Hayashi Rearrangement
European Journal of Organic Chemistry, 2009Co-Authors: Vanessa Gonnot, Cyril Antheaume, Marc Nicolas, Charles Mioskowski, Rachid BaatiAbstract:An expeditious, three-step synthesis of rhein (2) was optimized starting from bis(N,N-diethyl)-5-methoxybenzene-1,3-dicarboxamide. The key final step, involving deprotection/cyclization of ortho-benzoylbenzoic acid 9 in acidic chloroaluminate molten salts, yielded the desired natural product with high selectivity and good overall yield by precluding the competitive Hayashi Rearrangement.(© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)
