MARC details
| 000 -LEADER |
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| fixed length control field |
03978naaaa2200697uu 4500 |
| 001 - CONTROL NUMBER |
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| control field |
https://directory.doabooks.org/handle/20.500.12854/42797 |
| 005 - DATE AND TIME OF LATEST TRANSACTION |
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| control field |
20220714190722.0 |
| 020 ## - INTERNATIONAL STANDARD BOOK NUMBER |
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| International Standard Book Number |
books978-3-03921-949-0 |
| 020 ## - INTERNATIONAL STANDARD BOOK NUMBER |
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| International Standard Book Number |
9783039219483 |
| 020 ## - INTERNATIONAL STANDARD BOOK NUMBER |
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| International Standard Book Number |
9783039219490 |
| 024 7# - OTHER STANDARD IDENTIFIER |
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| Standard number or code |
10.3390/books978-3-03921-949-0 |
| Terms of availability |
doi |
| 041 0# - LANGUAGE CODE |
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| Language code of text/sound track or separate title |
English |
| 042 ## - AUTHENTICATION CODE |
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| Authentication code |
dc |
| 100 1# - MAIN ENTRY--PERSONAL NAME |
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| Personal name |
Díez, David |
| Relator code |
auth |
| 9 (RLIN) |
1612109 |
| 245 10 - TITLE STATEMENT |
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| Title |
Catalyzed Synthesis of Natural Products |
| 260 ## - PUBLICATION, DISTRIBUTION, ETC. (IMPRINT) |
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| Name of publisher, distributor, etc |
MDPI - Multidisciplinary Digital Publishing Institute |
| Date of publication, distribution, etc |
2019 |
| 300 ## - PHYSICAL DESCRIPTION |
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| Extent |
1 electronic resource (82 p.) |
| 506 0# - RESTRICTIONS ON ACCESS NOTE |
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| Terms governing access |
Open Access |
| Source of term |
star |
| Standardized terminology for access restriction |
Unrestricted online access |
| 520 ## - SUMMARY, ETC. |
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| Summary, etc |
Natural products have been a source of inspiration for chemists and chemical biologists for many years, and have a special relevance in the chemical space. In recent years, several novel synthetic strategies have appeared, such as diversity-oriented synthesis (DOS), biological-oriented synthesis (BiOS), and function-oriented synthesis (FOS), for accessing complex and functionally diverse molecules. In this manner, the synthesis of natural products has evolved towards simpler and ecological methods using biotransformation, combinatorial chemistry, or organocatalysts. In this issue, Prof. Chojnacka shows demonstrates the use of immobilized lipases as catalysts to aid in the synthesis of phosphatidylcholine enriched with myristic acid. Profs. Vila and Pedro used catalysts derived from (S)-mandelic acid to achieve the catalytic enantioselective addition of dimethylzinc to isatins. Prof. Diez shows the possibility of the obtention of 7,8-carvone epoxides in a diastereoselective manner using proline, quinidine, and diphenylprolinol as organocatalysts. A cheap, simple, clean, and scalable method involves the use of deep eutectic mixtures as reaction media, and Profs. Alonso and Guillena describe the use of this methodology for the enantioselective, organocatalyzed ?-amination of 1,3-dicarbonyl compounds. Biotransformations have been one of the methodologies for more efficient synthesis of natural products. Prof. Wu transforms ergostane triterpenoid antcin K using Psychrobacillus sp. Ak 187. Finally, Prof. Kovayashi reviews the total synthesis and biological evaluation of phaeosphaerides. The reader, through this issue, could gain an idea of the new directions that the synthesis of natural products using catalysts will have in the years to come. |
| 540 ## - TERMS GOVERNING USE AND REPRODUCTION NOTE |
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| Terms governing use and reproduction |
Creative Commons |
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https://creativecommons.org/licenses/by-nc-nd/4.0/ |
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cc |
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https://creativecommons.org/licenses/by-nc-nd/4.0/ |
| 546 ## - LANGUAGE NOTE |
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| Language note |
English |
| 653 ## - INDEX TERM--UNCONTROLLED |
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| Uncontrolled term |
n/a |
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structured phosphatidylcholine |
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carvone |
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| Uncontrolled term |
immobilized lipases |
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trimyristin |
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3-hydroxyoxindole |
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green chemistry |
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structural revision |
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anticancer |
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triterpenoid |
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organocatalysis |
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| Uncontrolled term |
natural products |
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epoxidation |
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?-amination |
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benzimidazole |
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total synthesis |
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zinc |
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Antrodia cinnamomea |
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aminocatalysis |
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epoxide |
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asymmetric organocatalysis |
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mandelamides |
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STAT3 |
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asymmetric catalysis |
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Psychrobacillus |
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isatin |
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chiral ?-hydroxyamide |
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interesterification |
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proline |
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phaeosphaeride B |
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| Uncontrolled term |
biotransformation |
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| Uncontrolled term |
phaeosphaeride A |
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| Uncontrolled term |
myristic acid |
| 653 ## - INDEX TERM--UNCONTROLLED |
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| Uncontrolled term |
egg-yolk phosphatidylcholine |
| 653 ## - INDEX TERM--UNCONTROLLED |
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| Uncontrolled term |
acidolysis |
| 653 ## - INDEX TERM--UNCONTROLLED |
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| Uncontrolled term |
antcin K |
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| Uncontrolled term |
deep eutectic solvents |
| 856 40 - ELECTRONIC LOCATION AND ACCESS |
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| Host name |
www.oapen.org |
| Uniform Resource Identifier |
<a href="https://mdpi.com/books/pdfview/book/1898">https://mdpi.com/books/pdfview/book/1898</a> |
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0 |
| Public note |
DOAB: download the publication |
| 856 40 - ELECTRONIC LOCATION AND ACCESS |
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| Host name |
www.oapen.org |
| Uniform Resource Identifier |
<a href="https://directory.doabooks.org/handle/20.500.12854/42797">https://directory.doabooks.org/handle/20.500.12854/42797</a> |
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0 |
| Public note |
DOAB: description of the publication |
