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pro vyhledávání: '"Yen-Ku Wu"'
94
The first part of this thesis describes the use of the Diels-Alder cycloaddition reaction between diester 36 and diene 52 for the purpose of achieving the total synthesis of natural products of a high degree of structural complexity. Specific
The first part of this thesis describes the use of the Diels-Alder cycloaddition reaction between diester 36 and diene 52 for the purpose of achieving the total synthesis of natural products of a high degree of structural complexity. Specific
Externí odkaz:
http://ndltd.ncl.edu.tw/handle/44018031100609014601
Publikováno v:
The Journal of Organic Chemistry. 88:6548-6552
The oxidative cleavage of C═C bonds with molecular oxygen was promoted effectively by a catalytic amount of a decatungstate photocatalyst using black light irradiation (365 nm). Not only aromatic ketones but also aliphatic ketones were obtained by
Publikováno v:
Bulletin of the Chemical Society of Japan. 95:1501-1505
Autor:
Xin‐Jie Lin, Shih‐Peng Huang, Min‐Jie Huang, Chien‐Lung Wang, Chi‐How Peng, Hsueh‐Ju Liu, Yen‐Ku Wu
Publikováno v:
Journal of the Chinese Chemical Society. 69:1803-1809
Publikováno v:
Advanced Synthesis & Catalysis. 364:1039-1043
Publikováno v:
Organic & Biomolecular Chemistry. 20:8212-8216
A photoflow method is presented for a radical-based coupling of unactivated arenes and aryl chlorides. The process proceeded smoothly at ambient temperature under metal-free conditions. Of note is that the reaction conditions are fine-tuned for chlor
Publikováno v:
Colloids and Surfaces A: Physicochemical and Engineering Aspects. 670:131525
Autor:
Yi Ching Lin, Yen-Ku Wu
Publikováno v:
Journal of the Chinese Chemical Society. 68:1812-1828
Publikováno v:
Organic & Biomolecular Chemistry. 20:6193-6195
A concise total synthesis of racemic mersicarpine is achieved featuring an application of a 6-exo-trig radical cyclization of a 2-indolyl radical.
Publikováno v:
Chemical Communications. 57:12119-12122
A method is presented for the synthesis of diaryl cyclic vinylogous esters. The sequence of C(sp3)–H arylation events is programed under the differentiated reactivity of the aryl halides, and the optimized reaction system is effectively diverted fr