Synthesis of cis- or trans-2,4-Disubstituted Tetrahydrofurans Bearing Amino and Imidazole Groups by Efficient Use of the Modified or Standard Mitsunobu Cyclization: Synthetic Studies Toward Novel Histamine H<sub>3</sub>-Ligands.

ARAKI L; HARUSAWA S; IJICHI I; OHISHI H; KURIHARA T

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J-GLOBAL ID：200902102131668570 Reference number：01A0568665

Synthesis of cis- or trans-2,4-Disubstituted Tetrahydrofurans Bearing Amino and Imidazole Groups by Efficient Use of the Modified or Standard Mitsunobu Cyclization: Synthetic Studies Toward Novel Histamine H₃-Ligands.

変形または標準Mitsunobu反応を効率的に用いるアミノおよびイミダゾール環を有するcis-またはtrans-二置換テトラヒドロフランの合成新規ヒスタミンH₃-リガンドの合成研究

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Author (5)： , , , ,
Material：
Volume： 55 Issue： 5 Page： 889-903 Publication year： May. 01, 2001
JST Material Number： S0966A ISSN： 0385-5414 CODEN： HTCYAM Document type： Article
Article type：原著論文 Country of issue： Japan (JPN) Language： ENGLISH (EN)

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Furans , Stereochemistry of organic reaction

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Synthesis of cis- or trans-2,4-Disubstituted Tetrahydrofurans Bearing Amino and Imidazole Groups by Efficient Use of the Modified or Standard Mitsunobu Cyclization: Synthetic Studies Toward Novel Histamine H3-Ligands.

Synthesis of cis- or trans-2,4-Disubstituted Tetrahydrofurans Bearing Amino and Imidazole Groups by Efficient Use of the Modified or Standard Mitsunobu Cyclization: Synthetic Studies Toward Novel Histamine H₃-Ligands.