Chiral Auxiliaries and Chirogenesis
This Reprint Book highlights and overviews the most important and novel aspects of chiral auxiliary and chirogenesis in different natural/physical sciences and in modern technologies. In particular, some newly emerging classes of molecules used for these purposes are described. This book consists of...
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Format: | Electronic Book Chapter |
Language: | English |
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Basel, Switzerland
MDPI - Multidisciplinary Digital Publishing Institute
2021
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Online Access: | DOAB: download the publication DOAB: description of the publication |
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020 | |a books978-3-0365-1017-0 | ||
020 | |a 9783036510163 | ||
020 | |a 9783036510170 | ||
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024 | 7 | |a 10.3390/books978-3-0365-1017-0 |c doi | |
041 | 0 | |a eng | |
042 | |a dc | ||
072 | 7 | |a GP |2 bicssc | |
100 | 1 | |a Borovkov, Victor |4 edt | |
700 | 1 | |a Borovkov, Victor |4 oth | |
245 | 1 | 0 | |a Chiral Auxiliaries and Chirogenesis |
260 | |a Basel, Switzerland |b MDPI - Multidisciplinary Digital Publishing Institute |c 2021 | ||
300 | |a 1 electronic resource (208 p.) | ||
336 | |a text |b txt |2 rdacontent | ||
337 | |a computer |b c |2 rdamedia | ||
338 | |a online resource |b cr |2 rdacarrier | ||
506 | 0 | |a Open Access |2 star |f Unrestricted online access | |
520 | |a This Reprint Book highlights and overviews the most important and novel aspects of chiral auxiliary and chirogenesis in different natural/physical sciences and in modern technologies. In particular, some newly emerging classes of molecules used for these purposes are described. This book consists of four review articles and one research paper and is of interest for general chemistry readership, including graduate and postgraduate students, and for researchers specializing in the fields of chirality and stereochemistry | ||
540 | |a Creative Commons |f https://creativecommons.org/licenses/by/4.0/ |2 cc |4 https://creativecommons.org/licenses/by/4.0/ | ||
546 | |a English | ||
650 | 7 | |a Research & information: general |2 bicssc | |
653 | |a buckybowl | ||
653 | |a corannulene | ||
653 | |a sumanene | ||
653 | |a bowl chirality | ||
653 | |a bowl inversion | ||
653 | |a asymmetric synthesis | ||
653 | |a chiral resolution | ||
653 | |a helicene | ||
653 | |a chiral auxiliaries | ||
653 | |a supramolecular chirogenesis | ||
653 | |a chirality | ||
653 | |a mechanical chirality | ||
653 | |a mecanostereochemistery | ||
653 | |a supramolecular chirality | ||
653 | |a rotaxane | ||
653 | |a aminolysis | ||
653 | |a heterocycle | ||
653 | |a receptors | ||
653 | |a enantioselective recognition | ||
653 | |a hydrogen bonding | ||
653 | |a conformational rigidity | ||
653 | |a configuration | ||
653 | |a diastereomeric interactions | ||
653 | |a macrocycle size | ||
653 | |a pyridine | ||
653 | |a dipolar interactions | ||
653 | |a cucurbiturils | ||
653 | |a hemicucurbiturils | ||
653 | |a symmetry breaking | ||
653 | |a helixes | ||
856 | 4 | 0 | |a www.oapen.org |u https://mdpi.com/books/pdfview/book/3949 |7 0 |z DOAB: download the publication |
856 | 4 | 0 | |a www.oapen.org |u https://directory.doabooks.org/handle/20.500.12854/76503 |7 0 |z DOAB: description of the publication |