Matches in SemOpenAlex for { <https://semopenalex.org/work/W4224293103> ?p ?o ?g. }
- W4224293103 abstract "Abstract 1,3‐Oxazolidines, derived from widely available enantiomerically pure 1,2‐aminoalcohols, are versatile chiral auxiliaries for several key transformations, often serving as a platform for inquiries into new and complex reactivity. This Review focuses on the chemistry of N‐acyl‐1,3‐oxazolidines in which the stereoselective transformation is carried out on the N‐acyl attached side chain of the molecule, covering reports from late 1980s to 2020 across several fields of asymmetric synthesis of bioactive molecules, and in particular of natural products." @default.
- W4224293103 created "2022-04-26" @default.
- W4224293103 creator A5020309444 @default.
- W4224293103 creator A5040539851 @default.
- W4224293103 creator A5050596094 @default.
- W4224293103 date "2022-05-12" @default.
- W4224293103 modified "2023-09-26" @default.
- W4224293103 title "Diastereoselective Functionalization of Chiral N‐Acyl‐1,3‐oxazolidines and Their Applications in the Synthesis of Bioactive Molecules" @default.
- W4224293103 cites W1773438220 @default.
- W4224293103 cites W1821893816 @default.
- W4224293103 cites W1967004108 @default.
- W4224293103 cites W1975133627 @default.
- W4224293103 cites W1977273715 @default.
- W4224293103 cites W1979040614 @default.
- W4224293103 cites W1979514860 @default.
- W4224293103 cites W1982750715 @default.
- W4224293103 cites W1984553867 @default.
- W4224293103 cites W1984591948 @default.
- W4224293103 cites W1988301386 @default.
- W4224293103 cites W1989568348 @default.
- W4224293103 cites W1991820997 @default.
- W4224293103 cites W1992539521 @default.
- W4224293103 cites W1993088940 @default.
- W4224293103 cites W2009345698 @default.
- W4224293103 cites W2011038397 @default.
- W4224293103 cites W2014555103 @default.
- W4224293103 cites W2015404405 @default.
- W4224293103 cites W2019206322 @default.
- W4224293103 cites W2019574712 @default.
- W4224293103 cites W2024617434 @default.
- W4224293103 cites W2025567014 @default.
- W4224293103 cites W2026054723 @default.
- W4224293103 cites W2027557698 @default.
- W4224293103 cites W2031335689 @default.
- W4224293103 cites W2033812609 @default.
- W4224293103 cites W2038374260 @default.
- W4224293103 cites W2039516668 @default.
- W4224293103 cites W2042703541 @default.
- W4224293103 cites W2046033650 @default.
- W4224293103 cites W2050815002 @default.
- W4224293103 cites W2051466730 @default.
- W4224293103 cites W2055059267 @default.
- W4224293103 cites W2061476523 @default.
- W4224293103 cites W2062927139 @default.
- W4224293103 cites W2065594788 @default.
- W4224293103 cites W2067447026 @default.
- W4224293103 cites W2069176783 @default.
- W4224293103 cites W2069501019 @default.
- W4224293103 cites W2069763602 @default.
- W4224293103 cites W2081244132 @default.
- W4224293103 cites W2086485392 @default.
- W4224293103 cites W2092069773 @default.
- W4224293103 cites W2095621360 @default.
- W4224293103 cites W2100391108 @default.
- W4224293103 cites W2108329468 @default.
- W4224293103 cites W2108362353 @default.
- W4224293103 cites W2109575174 @default.
- W4224293103 cites W2118614006 @default.
- W4224293103 cites W2128635703 @default.
- W4224293103 cites W2130889699 @default.
- W4224293103 cites W2137350736 @default.
- W4224293103 cites W2148594194 @default.
- W4224293103 cites W2168268012 @default.
- W4224293103 cites W2169037727 @default.
- W4224293103 cites W2323466954 @default.
- W4224293103 cites W2325739918 @default.
- W4224293103 cites W2329504033 @default.
- W4224293103 cites W2333274472 @default.
- W4224293103 cites W2333317045 @default.
- W4224293103 cites W2342187836 @default.
- W4224293103 cites W2557152552 @default.
- W4224293103 cites W2605810502 @default.
- W4224293103 cites W2748601993 @default.
- W4224293103 cites W2949331675 @default.
- W4224293103 cites W2949449248 @default.
- W4224293103 cites W2949872882 @default.
- W4224293103 cites W2950090813 @default.
- W4224293103 cites W2950157164 @default.
- W4224293103 cites W2950334424 @default.
- W4224293103 cites W2950374778 @default.
- W4224293103 cites W2950768844 @default.
- W4224293103 cites W2952180766 @default.
- W4224293103 cites W2952301161 @default.
- W4224293103 cites W2952491045 @default.
- W4224293103 cites W2952700619 @default.
- W4224293103 cites W2952860331 @default.
- W4224293103 cites W2952981329 @default.
- W4224293103 cites W2953049400 @default.
- W4224293103 cites W2953156755 @default.
- W4224293103 cites W2953344982 @default.
- W4224293103 cites W2953369802 @default.
- W4224293103 cites W2989728569 @default.
- W4224293103 cites W4236271345 @default.
- W4224293103 cites W4241594538 @default.
- W4224293103 cites W4243431528 @default.
- W4224293103 cites W4249748984 @default.
- W4224293103 doi "https://doi.org/10.1002/ejoc.202200267" @default.
- W4224293103 hasPublicationYear "2022" @default.
- W4224293103 type Work @default.
- W4224293103 citedByCount "2" @default.