1.

論文
論文
1. Synthesis of 3a-(indol-3-yl)-1,2,3,3a,8,8a-hexahydropyrrolo[2,3-b]indole core of leptosins D-F based on nucleophilic substitution reaction on indole nucleus
Yamada, Fumio ; Goto, Aya ; Somei, Masanori
出版情報: Heterocycles.  53  pp.1255-1258,  2000-06-01.  日本複素環化学研究所
URL: http://hdl.handle.net/2297/4359
概要: 金沢大学大学院自然科学研究科生理活性物質科学<br />金沢大学薬学部<br />A simple and convenient synthetic methodology for 3a-(indol-3-yl)- 1,2,3,3a,8,8 … a-hexahydropyrrolo[2,3-b]indole, the core structure of leptosins D-F is developed by applying nucleophilic substitution reaction of 1- hydroxytryptamines. 続きを見る
2.

論文
論文
2. Water-soluble melatonins: Syntheses of melatonins carrying a glycosyl group at the 1-position
Iwaki, Takako ; Fujita, Yasuaki ; Yamada, Fumio ; Somei, Masanori
出版情報: Heterocycles.  60  pp.1411-1418,  2003-06-01.  日本複素環化学研究所
URL: http://hdl.handle.net/2297/4376
概要: 金沢大学大学院自然科学研究科生理活性物質科学<br />金沢大学薬学部<br />1-(β-D-Xylopyranosyl)- (2a), 1-(β-D-glucopyranosyl)- (2b), 1-(β-D-galactopyrano … syl)- (2c), and 1-(α-D-arabinopyranosyl)melatonins (3b) are prepared as water-soluble melatonins starting from melatonin. 続きを見る
3.

論文
論文
3. The first and simple total synthesis of cappariloside A1
Somei, Masanori ; Yamada, Fumio
出版情報: Heterocycles.  53  pp.1573-1578,  2000-07-01.  日本複素環化学研究所
URL: http://hdl.handle.net/2297/4360
概要: 金沢大学大学院自然科学研究科生理活性物質科学<br />金沢大学薬学部<br />A lithium hydroxide promoted simple glycosylation of 4-hydroxyindole-3- acetoni … trile with 2,3,4, 6-tetra-O-acetyl-a-D-glucopyranosyl bromide was developed. Utilizing the method, the first and five steps total synthesis of cappariloside A was achieved from indole-3-carbaldehyde in 41% overall yield. 続きを見る