γ-Cyclodextrins possessing an azido group and a triisopropylbenzenesulfonyl group as useful synthetic and authentic intermediates for unsymmetrically functionalized derivatives-Reference-Cited by-同舟云学术

γ-Cyclodextrins possessing an azido group and a triisopropylbenzenesulfonyl group as useful synthetic and authentic intermediates for unsymmetrically functionalized derivatives

Published:2009-11 Issue:45 Volume:65 Page:9474-9480
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Himeno Yoshihide,Miyagawa Atsushi,Kawai Masao,Yamamura Hatsuo

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference28 articles.

1. Cyclodextrin-based class I aldolase enzyme mimics to catalyze crossed aldol condensations

2. Reversal of optical induction in transamination by regioisomeric bifunctionalized cyclodextrins1This paper is dedicated to the memory of Derek Barton, an extraordinary chemist and role model.1

3. Critical Difference in Chiral Recognition of N-Cbz-d/l-aspartic and -glutamic Acids by Mono- and Bis(Trimethylammonio)-β-cyclodextrins

4. Factors Controlling the Complex Architecture of Native and Modified Cyclodextrins with Dipeptide (Z-Glu-Tyr) Studied by Microcalorimetry and NMR Spectroscopy: Critical Effects of Peripheral Bis-trimethylamination and Cavity Size

5. Resolution and structural determination of unsymmetrically 6A6D-disubstituted .beta.-cyclodextrin

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