The effect of remote substitution on formation of preferential geometrical isomer of cobalt(III)–tetrazolato complexes formed via [2+3] cycloaddition

2013 ◽  
Vol 34 ◽  
pp. 62-67 ◽  
Author(s):  
Manideepa Saha ◽  
Rajendar Nasani ◽  
Shaikh M. Mobin ◽  
Biswarup Pathak ◽  
Suman Mukhopadhyay
Keyword(s):  
Science ◽  
1973 ◽  
Vol 181 (4100) ◽  
pp. 661-663 ◽  
Author(s):  
J. A. Klun ◽  
O. L. Chapman ◽  
K. C. Mattes ◽  
P. W. Wojtkowski ◽  
M. Beroza ◽  
...  

2019 ◽  
Author(s):  
Karim Bahou ◽  
D. Christopher Braddock ◽  
Adam G. Meyer ◽  
G. Paul Savage ◽  
Zhensheng Shi ◽  
...  

<b><u>Abstract:</u></b> A retrosynthetic disconnection-reconnection analysis of epoxypolyenes – substrates that can undergo cyclization to podocarpane-type tricycles – reveals relay-actuated Δ<sup>6,7</sup>-functionalized monoterpenoid alcohols for ruthenium benzylidene catalyzed olefin cross metathesis with homoprenyl benzenes. Successful implementation of this approach provided several epoxypolyenes as expected (<i>E</i>:<i>Z</i>, ca. 2-3:1). The method is further generalized for the cross metathesis of pre-existing trisubstituted olefins in other relay-actuated Δ<sup>6,7</sup>-functionalized monoterpenoid alcohols with various other trisubstituted alkenes to form new trisubstituted olefins. Epoxypolyene cyclization of an enantiomerically pure, but geometrically impure, epoxypolyene substrate provides an enantiomerically pure, trans-fused, podocarpane-type tricycle (from the <i>E</i>-geometrical isomer).<br>


1974 ◽  
Vol 27 (1) ◽  
pp. 71 ◽  
Author(s):  
NF Curtis

Preparations of N-rac- and N-meso-[Ni(l)][C1O4]2, N-meso-[Ni(l)(NCS)]2, N-rac-[{Ni(l)}2C2O4]-[ClO4]2, N-rac-[Co(l)acac][ClO4]2 and trans-N-rac-[Co(l)X2] ClO4, X = Cl-, Br-, OAc-, NO2- are reported [where (1)= C-meso-(5,7,12,14-tetraethyl-7,14-dimethyl-l,4,8,ll-tetraazacyclotetradeca-4,ll-diene)]. The p.m.r. spectra of N-rac- and N-meso-[Ni(l)]2+, some cobalt(111) derivatives of (1), and of [Ni (2)]2+, where (2) = C-meso-(5,7,12,14-tetraethyl-7,12-dimethyl-l,4,8,1l-tetraazacyclotetradeca-4,14-diene), a geometrical isomer of (1), are described. The configurational assignments are deduced from the chemical properties and p.m.r, spectra.


1998 ◽  
Vol 44 (4) ◽  
pp. 525-535 ◽  
Author(s):  
Nobuhiro FUKUDA ◽  
Masanori FUKUI ◽  
Yasuko KAI ◽  
Anura P. JAYASOORIYA ◽  
Masanobu SAKONO ◽  
...  

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