Remote acyclic stereocontrol. Chiral synthesis of (+)-pedamide
| ISSN: |
0040-4020
|
|---|---|
| Source: |
Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
|
| Topics: |
Chemistry and Pharmacology
|
| Type of Medium: |
Electronic Resource
|
| URL: |
| _version_ | 1798291344847798273 |
|---|---|
| autor | Matsumoto, T. Matsuda, F. Hasegawa, K. Yanagiya, M. |
| autorsonst | Matsumoto, T. Matsuda, F. Hasegawa, K. Yanagiya, M. |
| book_url | http://linkinghub.elsevier.com/retrieve/pii/0040-4020(84)80017-4 |
| datenlieferant | nat_lic_papers |
| fussnote | Synthesis of optically active pedamide (3), one of the tetrahydropyran moieties of the potent insect poison pederine (1), has been accomplished through a new, remote controlled asymmetric reduction of a ketone as key step. |
| hauptsatz | hsatz_simple |
| identnr | NLZ175960712 |
| issn | 0040-4020 |
| journal_name | Tetrahedron |
| materialart | 1 |
| package_name | Elsevier |
| publikationsort | Amsterdam |
| publisher | Elsevier |
| reference | 40 (1984), S. 2337-2343 |
| search_space | articles |
| shingle_author_1 | Matsumoto, T. Matsuda, F. Hasegawa, K. Yanagiya, M. |
| shingle_author_2 | Matsumoto, T. Matsuda, F. Hasegawa, K. Yanagiya, M. |
| shingle_author_3 | Matsumoto, T. Matsuda, F. Hasegawa, K. Yanagiya, M. |
| shingle_author_4 | Matsumoto, T. Matsuda, F. Hasegawa, K. Yanagiya, M. |
| shingle_catch_all_1 | Matsumoto, T. Matsuda, F. Hasegawa, K. Yanagiya, M. Remote acyclic stereocontrol. Chiral synthesis of (+)-pedamide 0040-4020 00404020 Elsevier |
| shingle_catch_all_2 | Matsumoto, T. Matsuda, F. Hasegawa, K. Yanagiya, M. Remote acyclic stereocontrol. Chiral synthesis of (+)-pedamide 0040-4020 00404020 Elsevier |
| shingle_catch_all_3 | Matsumoto, T. Matsuda, F. Hasegawa, K. Yanagiya, M. Remote acyclic stereocontrol. Chiral synthesis of (+)-pedamide 0040-4020 00404020 Elsevier |
| shingle_catch_all_4 | Matsumoto, T. Matsuda, F. Hasegawa, K. Yanagiya, M. Remote acyclic stereocontrol. Chiral synthesis of (+)-pedamide 0040-4020 00404020 Elsevier |
| shingle_title_1 | Remote acyclic stereocontrol. Chiral synthesis of (+)-pedamide |
| shingle_title_2 | Remote acyclic stereocontrol. Chiral synthesis of (+)-pedamide |
| shingle_title_3 | Remote acyclic stereocontrol. Chiral synthesis of (+)-pedamide |
| shingle_title_4 | Remote acyclic stereocontrol. Chiral synthesis of (+)-pedamide |
| sigel_instance_filter | dkfz geomar wilbert ipn albert fhp |
| source_archive | Elsevier Journal Backfiles on ScienceDirect 1907 - 2002 |
| timestamp | 2024-05-06T08:31:08.893Z |
| titel | Remote acyclic stereocontrol. Chiral synthesis of (+)-pedamide |
| titel_suche | Remote acyclic stereocontrol. Chiral synthesis of (+)-pedamide Synthesis of optically active pedamide (3), one of the tetrahydropyran moieties of the potent insect poison pederine (1), has been accomplished through a new, remote controlled asymmetric reduction of a ketone as key step. |
| topic | V |
| uid | nat_lic_papers_NLZ175960712 |