Matches in SemOpenAlex for { <https://semopenalex.org/work/W2030391608> ?p ?o ?g. }
- W2030391608 endingPage "250" @default.
- W2030391608 startingPage "244" @default.
- W2030391608 abstract "Abstract We present a diastereoselective synthesis of disubstituted cyclopentane 8 having a nitrogen‐containing quaternary carbon center, which is found in axinellamine A ( 5 ) and related compounds. During this work, we found that the 1,3‐dipolar cycloaddition product 24 immediately underwent intramolecular redox reaction at the newly formed morpholin‐2‐one moiety, thus affording disubstituted cyclopentane containing a tertiary amine ( 9 ) stereoselectively in good yield. The amine 9 was successfully converted into guanidine 31 , which corresponds to 8 , through iminium cation–enamine isomerization." @default.
- W2030391608 created "2016-06-24" @default.
- W2030391608 creator A5015733925 @default.
- W2030391608 creator A5045629742 @default.
- W2030391608 creator A5060170878 @default.
- W2030391608 creator A5081995369 @default.
- W2030391608 creator A5011462771 @default.
- W2030391608 date "2012-10-18" @default.
- W2030391608 modified "2023-10-18" @default.
- W2030391608 title "Intramolecular 1,3-Dipolar Cycloaddition-Mediated Stereoselective Synthesis of Disubstituted Cyclopentane: A Simple Model for the Cyclopentane Ring System of Polycyclic Oroidine Alkaloids" @default.
- W2030391608 cites W1969162633 @default.
- W2030391608 cites W1970052195 @default.
- W2030391608 cites W1970408151 @default.
- W2030391608 cites W1971386256 @default.
- W2030391608 cites W1973306817 @default.
- W2030391608 cites W1974130722 @default.
- W2030391608 cites W1976422565 @default.
- W2030391608 cites W1977965323 @default.
- W2030391608 cites W1978481031 @default.
- W2030391608 cites W1981308166 @default.
- W2030391608 cites W1981429606 @default.
- W2030391608 cites W1983978535 @default.
- W2030391608 cites W1986795310 @default.
- W2030391608 cites W1993607922 @default.
- W2030391608 cites W1998706858 @default.
- W2030391608 cites W2000824694 @default.
- W2030391608 cites W2002804752 @default.
- W2030391608 cites W2003701335 @default.
- W2030391608 cites W2005388938 @default.
- W2030391608 cites W2017822963 @default.
- W2030391608 cites W2019135498 @default.
- W2030391608 cites W2024091968 @default.
- W2030391608 cites W2024307148 @default.
- W2030391608 cites W2025005983 @default.
- W2030391608 cites W2025424415 @default.
- W2030391608 cites W2026566870 @default.
- W2030391608 cites W2028093561 @default.
- W2030391608 cites W2038739450 @default.
- W2030391608 cites W2041208437 @default.
- W2030391608 cites W2055165110 @default.
- W2030391608 cites W2058441883 @default.
- W2030391608 cites W2065169307 @default.
- W2030391608 cites W2065203107 @default.
- W2030391608 cites W2067866660 @default.
- W2030391608 cites W2067872683 @default.
- W2030391608 cites W2071402725 @default.
- W2030391608 cites W2078561475 @default.
- W2030391608 cites W2081850949 @default.
- W2030391608 cites W2092595111 @default.
- W2030391608 cites W2098601070 @default.
- W2030391608 cites W2100049908 @default.
- W2030391608 cites W2100793284 @default.
- W2030391608 cites W2106882567 @default.
- W2030391608 cites W2107494318 @default.
- W2030391608 cites W2119717285 @default.
- W2030391608 cites W2121829852 @default.
- W2030391608 cites W2123117845 @default.
- W2030391608 cites W2132819328 @default.
- W2030391608 cites W2135546524 @default.
- W2030391608 cites W2138115808 @default.
- W2030391608 cites W2140905597 @default.
- W2030391608 cites W2142741158 @default.
- W2030391608 cites W2157001985 @default.
- W2030391608 cites W2161998276 @default.
- W2030391608 cites W2163209669 @default.
- W2030391608 cites W2164895291 @default.
- W2030391608 cites W2165710041 @default.
- W2030391608 cites W2166424054 @default.
- W2030391608 cites W2171221083 @default.
- W2030391608 cites W2174997454 @default.
- W2030391608 cites W2320251481 @default.
- W2030391608 cites W2332757493 @default.
- W2030391608 cites W2343718732 @default.
- W2030391608 cites W2950730358 @default.
- W2030391608 cites W2950926355 @default.
- W2030391608 cites W2952357285 @default.
- W2030391608 cites W2952911301 @default.
- W2030391608 cites W2953082459 @default.
- W2030391608 cites W3004582800 @default.
- W2030391608 cites W4233823622 @default.
- W2030391608 cites W4235252170 @default.
- W2030391608 cites W4236589203 @default.
- W2030391608 cites W4242677955 @default.
- W2030391608 cites W4242934087 @default.
- W2030391608 cites W4248443108 @default.
- W2030391608 cites W4250694313 @default.
- W2030391608 cites W4251445356 @default.
- W2030391608 cites W4252932522 @default.
- W2030391608 cites W4256582782 @default.
- W2030391608 doi "https://doi.org/10.1002/asia.201200820" @default.
- W2030391608 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/23081863" @default.
- W2030391608 hasPublicationYear "2012" @default.
- W2030391608 type Work @default.
- W2030391608 sameAs 2030391608 @default.
- W2030391608 citedByCount "5" @default.
- W2030391608 countsByYear W20303916082014 @default.
- W2030391608 countsByYear W20303916082015 @default.
- W2030391608 countsByYear W20303916082016 @default.