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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Bibliographic Details
Other Authors: Borovkov, Victor (Editor)
Format: Book Chapter
Published: Basel, Switzerland MDPI - Multidisciplinary Digital Publishing Institute 2021
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Online Access:Get Fullteks
DOAB: description of the publication
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020 |a books978-3-0365-1017-0 
020 |a 9783036510163 
020 |a 9783036510170 
024 7 |a 10.3390/books978-3-0365-1017-0  |c doi 
041 0 |a English 
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.) 
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 Get Fullteks 
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