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SHIINA ESTERIFICATION

Shiina esterification

Shiina esterification is an organic chemical reaction that synthesizes carboxylic esters from nearly equal amounts of carboxylic acids and alcohols by

Shiina esterification

Shiina_esterification

Isamu Shiina

Japanese chemist

particular, the dehydration condensation reaction using MNBA (Shiina esterification and Shiina macrolactonization) is suitable for synthesis of unstable molecules

Isamu Shiina

Isamu_Shiina

Shiina macrolactonization

are employed. Shiina esterification Fischer-Speier esterification Steglich esterification Yamaguchi esterification Mitsunobu reaction Shiina, I.; Mukaiyama

Shiina macrolactonization

Shiina_macrolactonization

2-Methyl-6-nitrobenzoic anhydride

Chemical compound

for esterification, amidation, and peptide coupling. Condensation reaction Fischer-Speier esterification Mitsunobu reaction Shiina esterification Steglich

2-Methyl-6-nitrobenzoic anhydride

2-Methyl-6-nitrobenzoic_anhydride

List of organic reactions

aminohydroxylation Shenck ene reaction Shi epoxidation Shiina esterification Shiina macrolactonization or Shiina lactonization Sigmatropic reaction Simmons–Smith

List of organic reactions

List_of_organic_reactions

Tokyo University of Science

Private university in Japan

professor Isamu Shiina, professor, discoverer of 2-Methyl-6-nitrobenzoic anhydride, Shiina macrolactonization and Shiina esterification Yasuhiko Kojima

Tokyo University of Science

Tokyo_University_of_Science

Lactone

Cyclic carboxylic ester

an adjacent carboxylic acid. Specific methods include Yamaguchi esterification, Shiina macrolactonization, Corey-Nicolaou macrolactonization, Baeyer–Villiger

Lactone

Lanthanide trifluoromethanesulfonates

Triflate salts of the lanthanides

can just use water as the solvent. Ln(OTf)3 catalysts are used for esterifications. La(OTf)3 catalysts have been used for Diels-Alder, aldol, and allylation

Lanthanide trifluoromethanesulfonates

Lanthanide_trifluoromethanesulfonates

Mukaiyama Taxol total synthesis

steps (scheme 8) the amide tail 62 was added to ABCD ring 52 in an esterification catalysed by o,o'-di(2-pyridyl) thiocarbonate (DPTC) and DMAP forming

Mukaiyama Taxol total synthesis

Mukaiyama_Taxol_total_synthesis

Kedarcidin

Chemical compound

4-dimethylaminopyridine, and triethylamine as a base to promote intramolecular esterification. The means by which bacteria construct enediynes like kedarcidin continues

Kedarcidin