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Synthesis of Benzylated Cycloisomaltotri‐ and ‐hexaoside
Author(s) -
Houdier Stéphan,
Vottéro Philippe J. A.
Publication year - 1994
Publication title -
angewandte chemie international edition in english
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 0570-0833
DOI - 10.1002/anie.199403541
Subject(s) - trimer , natural product , product (mathematics) , chemistry , cyclodextrin , combinatorial chemistry , stereochemistry , organic chemistry , mathematics , geometry , dimer
The first benzylated 1,6 analogue (1) of natural α‐cyclodextrin was obtained as a side product in the I + ‐mediated reaction of a pentenyl isomaltotrioside. The main product was the expected trimer.
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