Facile chelation-controlled reductive opening of methoxybenzylidene acetals with Bu3SnH and MgBr2. Regioselective protection strategy as MPM ethers von Zheng, Bao-Zhong, Yamauchi, Megumi, Dei, Hiroo, Kusaka, Shin-ichi, Matsui, Katsuya, Yonemitsu, Osamu

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Stereoselective Hydrogenolysis of 1,1-Dibromo-1-alkenes and Stereospecific Synthesis of Conjugated (Z)-Alkenyl Compounds von Uenishi, Jun'ichi, Kawahama, Reiko, Yonemitsu, Osamu, Tsuji, Jiro

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Studies on the Synthesis of Myriaporones : Stereoselective Synthesis of the C5-C13 Fragment Starting from D-Glucose via Regioselective Reductive Opening of Methoxybenzylidene Aceta... von ZHENG, Bao-Zhong, YAMAUCHI, Megumi, DEI, Hiroo, YONEMITSU, Osamu

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Synthetic Studies of the 18-Membered Antitumor Macrolide, Tedanolide. 3. Stereocontrolled Synthesis of the C1-C12 Part via a Synthesis of the C1-C7 Fragment by a Mismatched but Eff... von MATSUSHIMA, Tomohiro, MORI, Michiko, ZHENG, Bao-Zhong, MAEDA, Hiroshi, NAKAJIMA, Noriyuki, UENISHI, Jun-ichi, YONEMITSU, Osamu

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Palladium-Catalyzed Stereoselective Hydrogenolysis of Conjugated 1,1-Dibromo-1-alkenes to (Z)-1-Bromo-1-alkenes. An Application to Stepwise and One-Pot Synthesis of Enediynes and D... von Uenishi, Jun'ichi, Kawahama, Reiko, Yonemitsu, Osamu, Tsuji, Jiro

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Synthesis of Chiral Nonracemic 1-(2-Pyridinyl)ethylamines:  Stereospecific Introduction of Amino Function onto the 2-Pyridinylmethyl Carbon Center von Uenishi, Jun'ichi, Hamada, Masahiro, Aburatani, Sachiko, Matsui, Katsuya, Yonemitsu, Osamu, Tsukube, Hiroshi

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A general and convenient synthetic method of geometrically pure ( Z)-1-bromo-1-alkenes von Uenishi, Jun'ichi, Kawahama, Reiko, Shiga, Yasuhiko, Yonemitsu, Osamu, Tsuji, Jiro

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Stereoselective Synthesis of Macrolide and Polyether Antibiotics von YONEMITSU, Osamu

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Molecular Recognition with Lanthanide(III) Tris(β-diketonate) Complexes:  Extraction, Transport, and Chiral Recognition of Unprotected Amino Acids von Tsukube, Hiroshi, Shinoda, Satoshi, Uenishi, Jun'ichi, Kanatani, Tatsuya, Itoh, Hiroyuki, Shiode, Mihoko, Iwachido, Tadashi, Yonemitsu, Osamu

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Stereocontrolled Synthesis of (11Z)-Retinal and Its Analogues von Uenishi, Jun'ichi, Kawahama, Reiko, Yonemitsu, Osamu, Wada, Akimori, Ito, Masayoshi

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Chiral Pyridines:  Optical Resolution of 1-(2-Pyridyl)- and 1-[6-(2,2‘-Bipyridyl)]ethanols by Lipase-Catalyzed Enantioselective Acetylation von Uenishi, Jun'ichi, Hiraoka, Takao, Hata, Shinichiro, Nishiwaki, Kenji, Yonemitsu, Osamu, Nakamura, Kaoru, Tsukube, Hiroshi

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Total Synthesis of (−)-Ircinianin and (+)-Wistarin von Uenishi, Jun'ichi, Kawahama, Reiko, Yonemitsu, Osamu

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A Facile Preparation of Geometrically Pure Alkenyl, Alkynyl, and Aryl Conjugated Z-Alkenes: Stereospecific Synthesis of Bombykol von Uenishi, Jun'ichi, Kawahama, Reiko, Izaki, Yoshiyuki, Yonemitsu, Osamu

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The first stereoselective total synthesis of lankanolide. Part 1: Computer-assisted design and lactonization of model seco-acid derivatives von Hamada, Tatsuo, Kobayashi, Yukinari, Kiyokawa, Mitsugu, Yonemitsu, Osamu

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Computer-assisted design and lactonization of model seco-acid derivatives of lankanolide von Hamada, Tatsuo, Kiyokawa, Mitsugu, Kobayashi, Yukinari, Yoshioka, Toshikazu, Sano, Junichiro, Yonemitsu, Osamu

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On the selectivity of deprotection of benzyl, mpm (4-methoxybenzyl) and dmpm (3,4-dimethoxybenzyl) protecting groups for hydroxy functions von Horita, Kiyoshi, Yoshioka, Tadao, Tanaka, Tatsuyoshi, Oikawa, Yuji, Yonemitsu, Osamu

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Stereoselective synthesis of erythronolide A via an extremely efficient macrolactonization by the modified Yamaguchi method von HIKOTA, M, TONE, H, HORITA, K, YONEMITSU, O

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MPM (4-methoxybenzyl) protection of hydroxy functions under mild acidic conditions von Nakajima, Noriyuki, Horita, Kiyoshi, Abe, Reiko, Yonemitsu, Osamu

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Synthesis of erythronolide a via a very efficient macrolactonization under usual acylation conditions with the Yamaguchi reagent von Hikota, Masataka, Sakurai, Youji, Horita, Kiyoshi, Yonemitsu, Osamu

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Synthetic studies of 18-membered anti-tumor macrolide, tedanolide. Computer-aided conformational design of a seco-acid derivative for efficient macrolactonization von Matsushima, Tomohiro, Horita, Kiyoshi, Nakajima, Noriyuki, Yonemitsu, Osamu

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