Catalyst-Control over Sixfold Stereogenicity

Author(s):  
Xingxing Wu ◽  
Reto M. Witzig ◽  
Rodolphe Beaud ◽  
Christian Fischer ◽  
Daniel Häussinger ◽  
...  

Governing higher-order stereogenicity is a long-standing goal in stereoselective catalysis, because it allows to achieve selectivity for more than a twofold number of stereoisomers per stereogenic unit. Current methods warrant control over the power of two stereoisomers and the configurations are routinely assigned using the descriptors ( R ) and ( S ), or related binary codes. In contrast, conformational analysis ranges beyond this dualistic treatment of stereoisomerism, which constitutes an unmet challenge for catalyst stereocontrolled processes. Herein, we now report that sixfold stereogenicity can be governed by stereoselective catalysis. By controlling a configurationally stable stereogenic axis with six large rotational barriers, a catalytic [2+2+2]-cyclotrimerization selectively governs the formation of one out of six stereoisomers with up to 0:0:2:98:0:0 stereocontrol. The underpinnings of conformational analysis and stereoselective catalysis are thereby conceptually reunited. Novel molecular architectures featuring distinct chemical topologies and unexplored chemical designs are anticipated from catalystcontrol over higher-order stereogenicities

2020 ◽  
Author(s):  
Xingxing Wu ◽  
Reto M. Witzig ◽  
Rodolphe Beaud ◽  
Christian Fischer ◽  
Daniel Häussinger ◽  
...  

Governing higher-order stereogenicity is a long-standing goal in stereoselective catalysis, because it allows to achieve selectivity for more than a twofold number of stereoisomers per stereogenic unit. Current methods warrant control over the power of two stereoisomers and the configurations are routinely assigned using the descriptors ( R ) and ( S ), or related binary codes. In contrast, conformational analysis ranges beyond this dualistic treatment of stereoisomerism, which constitutes an unmet challenge for catalyst stereocontrolled processes. Herein, we now report that sixfold stereogenicity can be governed by stereoselective catalysis. By controlling a configurationally stable stereogenic axis with six large rotational barriers, a catalytic [2+2+2]-cyclotrimerization selectively governs the formation of one out of six stereoisomers with up to 0:0:2:98:0:0 stereocontrol. The underpinnings of conformational analysis and stereoselective catalysis are thereby conceptually reunited. Novel molecular architectures featuring distinct chemical topologies and unexplored chemical designs are anticipated from catalystcontrol over higher-order stereogenicities


2005 ◽  
Vol 333 (3) ◽  
pp. 694-702 ◽  
Author(s):  
Kyoko Matoba ◽  
Mitsuyoshi Yamazoe ◽  
Kouta Mayanagi ◽  
Kosuke Morikawa ◽  
Sota Hiraga

ChemInform ◽  
2010 ◽  
Vol 28 (16) ◽  
pp. no-no
Author(s):  
S. E. BIALI ◽  
V. BOEHMER ◽  
S. COHEN ◽  
G. FERGUSON ◽  
C. GRUETTNER ◽  
...  

2005 ◽  
Vol 109 (5) ◽  
pp. 832-842 ◽  
Author(s):  
Vyacheslav S. Bryantsev ◽  
Timothy K. Firman ◽  
Benjamin P. Hay

1996 ◽  
Vol 118 (51) ◽  
pp. 12938-12949 ◽  
Author(s):  
Silvio E. Biali ◽  
Volker Böhmer ◽  
Shmuel Cohen ◽  
George Ferguson ◽  
Cordula Grüttner ◽  
...  

1974 ◽  
Vol 27 (6) ◽  
pp. 1227 ◽  
Author(s):  
SM Verma ◽  
Rao C Koteswara

A series of N'-sulphonyl and N'-acyl derivatives of N-aminobicyclo[2,2,1]hept-5-ene-endo-2,3-dicarboximide have been synthesized and their conformations have been investigated by N.M.R.spectroscopy. The effect of the sulphonyl group at the exocyclic nitrogen on the conformational process about the N-N bond has been studied. Existence of non-planar ground states about the N-N bond in the N',N?-disulphonyl and N'-sulphonyl-N'-acyl derivatives has been demonstrated.Temperature-dependent spectral changes have been related to the conformational changes about the N-N bond. It has been shown that the N'-tosyl substituent assumes a preferred conformation about the N-SO2 bond; the aryl part of the tosyl group lies exo to the cage-moiety. The N'-tosyl-N'-aroyl derivatives also show a preferred conformation about the N'-aroyl bond, the aryl part of the aroyl group lying endo to the cage-moiety. The N'-acetyl-N'-aroyl derivatives have been shown toexhibit low rotational barriers about the N'-aroyl bond.


1991 ◽  
Vol 47 (2) ◽  
pp. 284-288 ◽  
Author(s):  
D. G. Billing ◽  
J. C. A. Boeyens ◽  
L. Denner ◽  
K. E. Du Plooy ◽  
G. C. Long ◽  
...  

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