Matches in SemOpenAlex for { <https://semopenalex.org/work/W3210931677> ?p ?o ?g. }
- W3210931677 endingPage "328" @default.
- W3210931677 startingPage "307" @default.
- W3210931677 abstract "Abstract The current Account gives an insight into the synthesis of some N-heterocyclic β-amino acid derivatives and various functionalized saturated azaheterocycles accessed from substituted cycloalkenes via ring C=C bond oxidative cleavage followed by ring closing across double reductive amination. The ring-cleavage protocol has been accomplished according to two common approaches: a) Os-catalyzed dihydroxylation/NaIO4 vicinal diol oxidation and b) ozonolysis. A comparative study on these methodologies has been investigated. Due to the everincreasing relevance of organofluorine chemistry in drug research as well as of the high biological potential of β-amino acid derivatives several illustrative examples to the access of various fluorine-containing piperidine or azepane β-amino acid derivatives are also presented in the current Account. 1 Introduction 2 Olefin-Bond Transformation by Oxidative Ring Cleavage 3 Synthesis of Saturated Azaheterocycles via Oxidative Ring-Opening/Ring-Closing Double Reductive Amination 3.1 Importance of Fluorine-Containing Azaheterocycles in Pharmaceutical Research 3.2 Synthesis of Azaheterocyclic Amino Acid Derivatives with a Piperidine or Azepane Framework through Oxidative Ring Opening/Reductive Amination 3.2.1 Synthesis of Piperidine β-Amino Esters 3.2.2 Synthesis of Azepane β-Amino Esters 3.2.3 Synthesis of Fluorine-Containing Piperidine γ-Amino Esters 3.3 Synthesis of Tetrahydroisoquinoline Derivatives through Oxidative Ring Opening/Reductive Amination Protocol 3.4 Synthesis of Functionalized Benzazepines through Reductive Amination 3.4.1 Synthesis of Benzo[c]azepines 3.4.2 Synthesis of Benzo[d]azepines 3.5 Synthesis of Various N-Heterocycles via Ozonolysis/Reductive Amination 3.5.1 Synthesis of Compounds with an Azepane Ring 3.5.2 Synthesis of Piperidine β-Amino Acids and Piperidine-Fused β-Lactams 3.5.3 Synthesis of γ-Lactams with a Piperidine Ring 3.5.4 Synthesis of other N-Heterocycles 4 Summary and Outlook 5 List of Abbreviations" @default.
- W3210931677 created "2021-11-08" @default.
- W3210931677 creator A5004527080 @default.
- W3210931677 creator A5008062538 @default.
- W3210931677 creator A5025927095 @default.
- W3210931677 creator A5058365521 @default.
- W3210931677 date "2021-11-03" @default.
- W3210931677 modified "2023-10-07" @default.
- W3210931677 title "Application of Oxidative Ring Opening/Ring Closing by Reductive Amination Protocol for the Stereocontrolled Synthesis of Functionalized Azaheterocycles" @default.
- W3210931677 cites W1765046296 @default.
- W3210931677 cites W1970067655 @default.
- W3210931677 cites W1973653019 @default.
- W3210931677 cites W1978420088 @default.
- W3210931677 cites W1987840514 @default.
- W3210931677 cites W1987935150 @default.
- W3210931677 cites W1988146957 @default.
- W3210931677 cites W1989694334 @default.
- W3210931677 cites W1990335500 @default.
- W3210931677 cites W1993491755 @default.
- W3210931677 cites W1993582784 @default.
- W3210931677 cites W1998871264 @default.
- W3210931677 cites W2003670034 @default.
- W3210931677 cites W2017372573 @default.
- W3210931677 cites W2033984611 @default.
- W3210931677 cites W2034649797 @default.
- W3210931677 cites W2037684408 @default.
- W3210931677 cites W2039933321 @default.
- W3210931677 cites W2050490886 @default.
- W3210931677 cites W2061312817 @default.
- W3210931677 cites W2068157329 @default.
- W3210931677 cites W2083344137 @default.
- W3210931677 cites W2083737305 @default.
- W3210931677 cites W2103698259 @default.
- W3210931677 cites W2104830778 @default.
- W3210931677 cites W2118223713 @default.
- W3210931677 cites W2127319983 @default.
- W3210931677 cites W2143506038 @default.
- W3210931677 cites W2143786105 @default.
- W3210931677 cites W2150104943 @default.
- W3210931677 cites W2154493821 @default.
- W3210931677 cites W2161802060 @default.
- W3210931677 cites W2166359822 @default.
- W3210931677 cites W2166896901 @default.
- W3210931677 cites W2168444131 @default.
- W3210931677 cites W2168632704 @default.
- W3210931677 cites W2171894480 @default.
- W3210931677 cites W2310460235 @default.
- W3210931677 cites W2319703220 @default.
- W3210931677 cites W2323897663 @default.
- W3210931677 cites W2324080322 @default.
- W3210931677 cites W2326309772 @default.
- W3210931677 cites W2326550954 @default.
- W3210931677 cites W2332445220 @default.
- W3210931677 cites W2407040666 @default.
- W3210931677 cites W2490681934 @default.
- W3210931677 cites W2525537368 @default.
- W3210931677 cites W2526216986 @default.
- W3210931677 cites W2527891505 @default.
- W3210931677 cites W2554028180 @default.
- W3210931677 cites W2558924372 @default.
- W3210931677 cites W2569173963 @default.
- W3210931677 cites W2581106965 @default.
- W3210931677 cites W2595708401 @default.
- W3210931677 cites W2604318173 @default.
- W3210931677 cites W2616823810 @default.
- W3210931677 cites W2701092419 @default.
- W3210931677 cites W2755619509 @default.
- W3210931677 cites W2755644819 @default.
- W3210931677 cites W2767645716 @default.
- W3210931677 cites W2776260466 @default.
- W3210931677 cites W2780619456 @default.
- W3210931677 cites W2792842263 @default.
- W3210931677 cites W2793383368 @default.
- W3210931677 cites W2886082479 @default.
- W3210931677 cites W2901630821 @default.
- W3210931677 cites W2901637190 @default.
- W3210931677 cites W2944496432 @default.
- W3210931677 cites W2945137288 @default.
- W3210931677 cites W2952402072 @default.
- W3210931677 cites W2953861973 @default.
- W3210931677 cites W2957991130 @default.
- W3210931677 cites W2964193653 @default.
- W3210931677 cites W2970709777 @default.
- W3210931677 cites W2972847614 @default.
- W3210931677 cites W2996669561 @default.
- W3210931677 cites W3003530150 @default.
- W3210931677 cites W3011727358 @default.
- W3210931677 cites W3011888142 @default.
- W3210931677 cites W3025817778 @default.
- W3210931677 cites W3037636504 @default.
- W3210931677 cites W3092980604 @default.
- W3210931677 cites W3110678364 @default.
- W3210931677 cites W3165656926 @default.
- W3210931677 cites W4291208076 @default.
- W3210931677 doi "https://doi.org/10.1055/s-0040-1719850" @default.
- W3210931677 hasPublicationYear "2021" @default.
- W3210931677 type Work @default.
- W3210931677 sameAs 3210931677 @default.