Reversible C–C bond formation: solid state structure of the aldol-like addition product of adamantanone to a 1,5-diazapentadienyllithium, and its solution state retro-aldol dissociationElectronic supplementary information (ESI) available: preparative and characterization details. See http://www.rsc.org/suppdata/cc/b2/b211745b/

2003 ◽  
pp. 744-745 ◽  
Author(s):  
Lee-Jon Ball ◽  
Anthony P. Dickie ◽  
Francis S. Mair ◽  
David A. Middleton ◽  
Robin G. Pritchard
Polyhedron ◽  
2019 ◽  
Vol 169 ◽  
pp. 266-277 ◽  
Author(s):  
Rami J. Batrice ◽  
Jennifer N. Wacker ◽  
Elliot N. Glass ◽  
Safia Z. Jilani ◽  
YuYe J. Tong ◽  
...  

1994 ◽  
Vol 98 (18) ◽  
pp. 4919-4922 ◽  
Author(s):  
Y. W. Kim ◽  
A. Labouriau ◽  
C. M. Taylor ◽  
William L. Earl ◽  
L. G. Werbelow

FEBS Letters ◽  
1994 ◽  
Vol 355 (2) ◽  
pp. 140-146 ◽  
Author(s):  
Gregory M. Lee ◽  
Chinpan Chen ◽  
Thomas M. Marschner ◽  
Niels H. Andersen

2015 ◽  
Vol 44 (36) ◽  
pp. 15938-15948 ◽  
Author(s):  
Michael R. Chapman ◽  
Benjamin R. M. Lake ◽  
Christopher M. Pask ◽  
Bao N. Nguyen ◽  
Charlotte E. Willans

Electronically diverse pyridyl-substituted Pd(ii)-NHC complexes have been employed in Suzuki–Miyaura cross-coupling to yield a sterically congested tetra-ortho-substituted biaryl product.


2014 ◽  
Vol 69 (11-12) ◽  
pp. 1269-1289 ◽  
Author(s):  
Bernd Wrackmeyer ◽  
Elena V. Klimkina ◽  
Wolfgang Milius ◽  
Christian Butterhof ◽  
Kathrin Inzenhofer

Abstract Alkynyl(ferrocenyl)vinylsilanes containing up to three alkynyl units were prepared and treated with 9-borabicyclo[3.3.1]nonane (9-BBN). All reactions proceeded in the beginning by regioselective 1,2-hydroboration of the vinyl group, with boron attached to the terminal carbon. This was followed by intra-molecular 1,1-carboboration, leading to fused silacarbacycles, depending on the number of C≡C bonds. Thus, new siloles and even fused siloles became available. The solution-state structures were revealed by multinuclear NMR techniques (1H, 11B, 13C, 29Si NMR), complemented by calculated single-molecule structures and calculated NMR parameters at the B3LYP/6-311+G(d,p) level of theory. In one case, the solid-state structure of a bicyclic derivative was determined.


2014 ◽  
Vol 20 (44) ◽  
pp. 14201-14206 ◽  
Author(s):  
Udaya Kiran Marelli ◽  
Andreas O. Frank ◽  
Bernhard Wahl ◽  
Valeria La Pietra ◽  
Ettore Novellino ◽  
...  

2000 ◽  
Vol 57 (1) ◽  
pp. o81-o82 ◽  
Author(s):  
Philip J. Cox ◽  
Margot Fergusson ◽  
Lutfun Nahar ◽  
Satyajit D. Sarker

The solid state structure of moschamindole {systematic name: 10-[2-(4-hydroxy-3-methoxyphenyl)]-1,2,3,4,10,10a-hexahydro-6H-furo[2,3,4-jk]pyrrolo[4,3,2-ef]-3-benzazocin-1-one}, C20H18N2O4is similar to its solution state structure, previously determined by NMR, and evidence of intermolecular hydrogen bonding is now presented.


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