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HORIUCHI ITAROU SHOTEN KK
Original Assignee
HORIUCHI ITAROU SHOTEN KK
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Filing date
Publication date
Application filed by HORIUCHI ITAROU SHOTEN KKfiledCriticalHORIUCHI ITAROU SHOTEN KK
Priority to JP59061224ApriorityCriticalpatent/JPS60204787A/ja
Publication of JPS60204787ApublicationCriticalpatent/JPS60204787A/ja
Publication of JPH047349B2publicationCriticalpatent/JPH047349B2/ja
Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
Y02P20/00—Technologies relating to chemical industry
Y02P20/50—Improvements relating to the production of bulk chemicals
Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
Landscapes
Low-Molecular Organic Synthesis Reactions Using Catalysts
(AREA)
Structure of batrachotoxin, a steroidal alkaloid from the Colombian arrow poison frog, Phyllobates aurotaenia, and partial synthesis of batrachotoxin and its analogs and homologs
meso-and dl-Bivalvane (pentasecododecahedrane). Enantiomer recognition during reductive coupling of racemic and chiral 2, 3-dihydro-and hexahydrotriquinacen-2-ones
Antitumour benzothiazoles 13.(Diacetoxy) iodobenzene (DAIB) oxidation of 2-(4-hydroxy-3-methoxyphenyl)-benzothiazole and related compounds in the presence of dienophiles.
A new approach to synthesis of vinblastine analogs. Addition of organozinc reagents to the dihydropyridinium ion generated by fragmentative coupling to catharanthine and vindoline.
Synthesis and complete assignments of 1H and 13C NMR spectra of mesoionic 2-(ptrifluoromethylphenyl)-3-methyl-4-(p-tolyl)-1, 3-thiazolium-5-thiolate and 2-(p-chlorophenyl)-3-methyl–4-(p-isopropylphenyl)-1, 3-thiazolium-5-thiolate