On the mechanism of effectively chiral‐pure macromolecular spiralization induced by a weakly chiral polarized heterochiral solution of a chiral compound

Chirality ◽  
2021 ◽  
Author(s):  
Аleksey А. Skoblin ◽  
Maria G. Mikhaleva ◽  
Lyubov I. Voronina ◽  
Sergey V. Stovbun
Keyword(s):  
2019 ◽  
Vol 19 (25) ◽  
pp. 2348-2356 ◽  
Author(s):  
Neng-Zhong Xie ◽  
Jian-Xiu Li ◽  
Ri-Bo Huang

Acetoin is an important four-carbon compound that has many applications in foods, chemical synthesis, cosmetics, cigarettes, soaps, and detergents. Its stereoisomer (S)-acetoin, a high-value chiral compound, can also be used to synthesize optically active drugs, which could enhance targeting properties and reduce side effects. Recently, considerable progress has been made in the development of biotechnological routes for (S)-acetoin production. In this review, various strategies for biological (S)- acetoin production are summarized, and their constraints and possible solutions are described. Furthermore, future prospects of biological production of (S)-acetoin are discussed.


1999 ◽  
Vol 26 (12) ◽  
pp. 1805-1811 ◽  
Author(s):  
Yu. I. Yuzyuk ◽  
S. Sarmento ◽  
P. Simeao Carvalho ◽  
A. Almeida ◽  
Filipa Pinto ◽  
...  

1989 ◽  
Vol 175 ◽  
Author(s):  
S.H. Chen ◽  
M.L. Tsai ◽  
S.D. Jacobs

AbstractChiral nematic copolymers based on optically active cholesterol, dihydrocholesterol, (R)-(+)- and (S)-(−)-1-phenylethylamine, and (+)- and (−)- isopinocampheol were synthesized and characterized for the investigations of thermotropic and optical properties. Although helical sense does not appear to correlate with the sign of [α]D of the precursor chiral compound as suggested by the observations of cholesteryl and dihydrocholesteryl copolymers, the inversion of chirality in the pendant group, (R)-(+)- vs (S)-(−)-1-phenylethylamine, does lead to the opposite handedness in the resultant helical structure. To better understand the structure-property relationships involving helical sense and twisting power, systematic studies of the roles played by both nematogenic and chiral structures as well as other structural features of the comonomers should be conducted.


2005 ◽  
Vol 15 (32) ◽  
pp. 3285 ◽  
Author(s):  
Atsushi Yoshizawa ◽  
Masatada Sato ◽  
Juri Rokunohe
Keyword(s):  

1983 ◽  
Vol 44 (5) ◽  
pp. 623-629 ◽  
Author(s):  
A.M. Levelut ◽  
C. Germain ◽  
P. Keller ◽  
L. Liebert ◽  
J. Billard
Keyword(s):  

2011 ◽  
Vol 307 (1) ◽  
pp. 110-112 ◽  
Author(s):  
Henning Kaemmerer ◽  
Ronald Zinke ◽  
Heike Lorenz ◽  
Matthew J. Jones ◽  
Andreas Seidel-Morgenstern ◽  
...  

2021 ◽  
Vol 77 (3) ◽  
pp. 152-160
Author(s):  
Philipp Honegger ◽  
Alexander Roller ◽  
Michael Widhalm

In the course of an ongoing synthetic project on cyclic diferrocenylphosphines, we obtained a group of planar–chiral diferrocenyl compounds useful as precursors for subsequent cyclization. Here we report the crystal structures of two symmetric compounds [(FcA)2(Ph)P], one of which contains four stereogenic centres (two C chiral and two planar chiral centres), i.e. 1,1′-(phenylphosphanediyl)bis{(2S p)-2-[(1R)-1-(acetyloxy)ethyl]ferrocene}, [Fe2(C5H5)2(C24H25O4P)], and the other phosphine sulfide is a purely planar–chiral compound (two planar chiral centres), i.e. bis[(2S p)--2-ethenylferrocen-1-yl]phenylphosphane sulfide, [Fe2(C5H5)2(C20H17PS)]. Owing to the stereocentres present, reactions performed on [(FcA)2(Ph)P]-type compounds strongly favour one ferrocene unit over the other due to diastereoselectivity. Furthermore, we present four related structures where the ferrocene units are not identical [(FcA)(FcB)(Ph)P]. These are {(2S p)-2-[(1R)-1-(acetyloxy)ethyl]ferrocen-1-yl}[(2S p)-2-ethenylferrocen-1-yl]phenyl-(S)-phosphine sulfide, [Fe2(C5H5)2(C22H21O2PS)], [(2S p)-2-ethenylferrocen-1-yl]{(2S p)-2-[(1R)-1-hydroxyethyl]ferrocen-1-yl}phenyl-(S)-phosphine sulfide, [Fe2(C5H5)2(C20H19OPS)], {(2S p)-2-[(1R)-1-(acetyloxy)ethyl]ferrocen-1-yl}{(2S p)-2-[(1R)-1-hydroxyethyl]ferrocen-1-yl}phenyl-(R)-phosphine sulfide, [Fe2(C5H5)2(C22H23O3PS)], and {(2S p)-2-[(1R)-1-benzylamino)ethyl]ferrocen-1-yl}[(2S p)-2-ethenylferrocen-1-yl]phenyl-(S)-phosphine sulfide, [Fe2(C5H5)2(C27H26NPS)]. All of the structures are accessible in one step from known precursors.


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