Synthetic studies on quinocarcin and its related compounds. 2. - Synthesis of an enantiomeric pair of the ABC ring system of quinocarcin
Saito, S. ; Tanaka, K. ; Nakatani, K. ; Matsuda, F. ; Katoh, T. ; Terashima, S.
Amsterdam : Elsevier
Amsterdam : Elsevier
| ISSN: |
0040-4020
|
|---|---|
| Keywords: |
ABC ring system ; O-acetal formation ; antitumor antibiotic ; asymmetric synthesis ; diastereoselective reduction ; intramolecular N ; quinocarcin
|
| Source: |
Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
|
| Topics: |
Chemistry and Pharmacology
|
| Type of Medium: |
Electronic Resource
|
| URL: |
| _version_ | 1798291335728332800 |
|---|---|
| autor | Saito, S. Tanaka, K. Nakatani, K. Matsuda, F. Katoh, T. Terashima, S. |
| autorsonst | Saito, S. Tanaka, K. Nakatani, K. Matsuda, F. Katoh, T. Terashima, S. |
| book_url | http://linkinghub.elsevier.com/retrieve/pii/S0040-4020(01)80642-6 |
| datenlieferant | nat_lic_papers |
| fussnote | An enantiomeric pair of the ABC ring system (5 and ent-5) of quinocarcin (1), a potent antitumor antibiotic, was synthesized in 〉 95% ee w | The title compounds (5, ent-5, 39, and ent-39) were synthesized by featuring novel diastereoselective reduction of 1,3-disubst |
| hauptsatz | hsatz_simple |
| identnr | NLZ175878501 |
| issn | 0040-4020 |
| journal_name | Tetrahedron |
| materialart | 1 |
| package_name | Elsevier |
| publikationsort | Amsterdam |
| publisher | Elsevier |
| reference | 50 (1994), S. 6209-6220 |
| schlagwort | ABC ring system O-acetal formation antitumor antibiotic asymmetric synthesis diastereoselective reduction intramolecular N quinocarcin |
| search_space | articles |
| shingle_author_1 | Saito, S. Tanaka, K. Nakatani, K. Matsuda, F. Katoh, T. Terashima, S. |
| shingle_author_2 | Saito, S. Tanaka, K. Nakatani, K. Matsuda, F. Katoh, T. Terashima, S. |
| shingle_author_3 | Saito, S. Tanaka, K. Nakatani, K. Matsuda, F. Katoh, T. Terashima, S. |
| shingle_author_4 | Saito, S. Tanaka, K. Nakatani, K. Matsuda, F. Katoh, T. Terashima, S. |
| shingle_catch_all_1 | Saito, S. Tanaka, K. Nakatani, K. Matsuda, F. Katoh, T. Terashima, S. Synthetic studies on quinocarcin and its related compounds. 2. - Synthesis of an enantiomeric pair of the ABC ring system of quinocarcin ABC ring system O-acetal formation antitumor antibiotic asymmetric synthesis diastereoselective reduction intramolecular N quinocarcin ABC ring system O-acetal formation antitumor antibiotic asymmetric synthesis diastereoselective reduction intramolecular N quinocarcin 0040-4020 00404020 Elsevier |
| shingle_catch_all_2 | Saito, S. Tanaka, K. Nakatani, K. Matsuda, F. Katoh, T. Terashima, S. Synthetic studies on quinocarcin and its related compounds. 2. - Synthesis of an enantiomeric pair of the ABC ring system of quinocarcin ABC ring system O-acetal formation antitumor antibiotic asymmetric synthesis diastereoselective reduction intramolecular N quinocarcin ABC ring system O-acetal formation antitumor antibiotic asymmetric synthesis diastereoselective reduction intramolecular N quinocarcin 0040-4020 00404020 Elsevier |
| shingle_catch_all_3 | Saito, S. Tanaka, K. Nakatani, K. Matsuda, F. Katoh, T. Terashima, S. Synthetic studies on quinocarcin and its related compounds. 2. - Synthesis of an enantiomeric pair of the ABC ring system of quinocarcin ABC ring system O-acetal formation antitumor antibiotic asymmetric synthesis diastereoselective reduction intramolecular N quinocarcin ABC ring system O-acetal formation antitumor antibiotic asymmetric synthesis diastereoselective reduction intramolecular N quinocarcin 0040-4020 00404020 Elsevier |
| shingle_catch_all_4 | Saito, S. Tanaka, K. Nakatani, K. Matsuda, F. Katoh, T. Terashima, S. Synthetic studies on quinocarcin and its related compounds. 2. - Synthesis of an enantiomeric pair of the ABC ring system of quinocarcin ABC ring system O-acetal formation antitumor antibiotic asymmetric synthesis diastereoselective reduction intramolecular N quinocarcin ABC ring system O-acetal formation antitumor antibiotic asymmetric synthesis diastereoselective reduction intramolecular N quinocarcin 0040-4020 00404020 Elsevier |
| shingle_title_1 | Synthetic studies on quinocarcin and its related compounds. 2. - Synthesis of an enantiomeric pair of the ABC ring system of quinocarcin |
| shingle_title_2 | Synthetic studies on quinocarcin and its related compounds. 2. - Synthesis of an enantiomeric pair of the ABC ring system of quinocarcin |
| shingle_title_3 | Synthetic studies on quinocarcin and its related compounds. 2. - Synthesis of an enantiomeric pair of the ABC ring system of quinocarcin |
| shingle_title_4 | Synthetic studies on quinocarcin and its related compounds. 2. - Synthesis of an enantiomeric pair of the ABC ring system of quinocarcin |
| sigel_instance_filter | dkfz geomar wilbert ipn albert fhp |
| source_archive | Elsevier Journal Backfiles on ScienceDirect 1907 - 2002 |
| timestamp | 2024-05-06T08:31:00.148Z |
| titel | Synthetic studies on quinocarcin and its related compounds. 2. - Synthesis of an enantiomeric pair of the ABC ring system of quinocarcin |
| titel_suche | Synthetic studies on quinocarcin and its related compounds. 2. - Synthesis of an enantiomeric pair of the ABC ring system of quinocarcin An enantiomeric pair of the ABC ring system (5 and ent-5) of quinocarcin (1), a potent antitumor antibiotic, was synthesized in 〉 95% ee w | The title compounds (5, ent-5, 39, and ent-39) were synthesized by featuring novel diastereoselective reduction of 1,3-disubst |
| topic | V |
| uid | nat_lic_papers_NLZ175878501 |