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Enantioselective Bronsted acid catalyzed addition reactions of methyleneaminopyrrolidine to imines

Abstract:
A new series of BINOL-derived multidentate Brønsted acid catalysts has been developed for the enantioselective addition of the d 1-synthon, methyleneaminopyrrolidine, to N-Boc imines, yielding the versatile, protected α-aminohydrazone intermediates in moderate to good ee. © Georg Thieme Verlag Stuttgart.
Publication status:
Published

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Publisher copy:
10.1055/s-2005-917098

Authors


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Institution:
University of Oxford
Department:
Oxford, MPLS, Chemistry, Organic Chemistry
Tillman, AL More by this author
Journal:
SYNLETT
Issue:
17
Pages:
2635-2638
Publication date:
2005-10-17
DOI:
EISSN:
1437-2096
ISSN:
0936-5214
URN:
uuid:a28bdac5-2ebe-413f-b3ac-d09631af0b1a
Source identifiers:
39703
Local pid:
pubs:39703

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