𝔖 Bobbio Scriptorium
✦   LIBER   ✦

3,6,9-trioxanthracenes and 3,6-dioxa-9-thianthracenes: Conformational analysis and complete assignment of 13C NMR spectra

✍ Scribed by Marcial Moreno-Mañas; Jordi Ribas; Francisco Sánchez-Ferrando; Albert Virgili


Publisher
John Wiley and Sons
Year
1987
Tongue
English
Weight
172 KB
Volume
25
Category
Article
ISSN
0749-1581

No coin nor oath required. For personal study only.

✦ Synopsis


The 20.15 MHz 13C NMR spectra of five 3,6,9-trioxanthracenes and four 3,6-dioxa-9-thianthracenes have been assigned using a variety of one-dimensional techniques. These include spin-echo multiplicity sorting (SEFT), long-range heteronuclear coupling constant determination via gated decoupling and selective heteronuclear 13C{ 'H} NOE difference spectroscopy. The axial position of substituents on C-10 has been demonstrated.


📜 SIMILAR VOLUMES


1H and 13C NMR spectra of C-6 and C-9 su
✍ Kirsten Goodall; Margaret Brimble; David Barker 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 168 KB

## Abstract The ^1^H and ^13^C NMR data for 3‐azabicyclo[3.3.1]nonanes with OH and OMe substituents at C‐6 and C‐9 were measured using 1D (DEPT) and 2D (COSY, HSQC, HMBC, NOESY) experiments. Comparison of this NMR data illustrates the effects of stereochemistry and substitution at these positions.

Complete Assignment of 1H and 13C NMR Sp
✍ J. G. Sośnicki; T. S. Jagodziński; B. Nowak-Wydra; P. E. Hansen 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 643 KB

The complete assignment of the 'H and 13C NMR spectra of two carbothioamide-substituted meroterpenes is presented. Resonance assignments were achieved by the use of one-and two-dimensional NMR, NOED, selective decoupling measurements and the deuterium isotope effect on the I3C chemical shifts. Six-m

Synthesis and complete assignment of the
✍ Pedro Besada; Tamara Costas; Noemi Vila; Carla Chessa; Carmen Terán 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 English ⚖ 116 KB

## Abstract Several pyridazin‐3(2__H__)‐one derivatives were synthesized starting from alkyl furans using oxidation with singlet oxygen to give 4‐methoxy or 4‐hydroxybutenolides, key intermediates of the synthetic strategy followed. For all pyridazinones reported, a complete assignment of the ^1^H

1H and 13C NMR spectral assignments of s
✍ Paramasivam Parthiban; Rajamanickam Ramachandran; Gopalakrishnan Aridoss; Sentha 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 136 KB

## Abstract The ^1^H and ^13^C NMR spectra of 2,4,6,8‐tetraaryl‐3,7‐diazabicyclo[3.3.1]nonan‐9‐ones (1–2), oximes (3–8) and __O__‐benzyl oximes (9–12) were recorded. The chemical shifts were unambiguously assigned using 1D and 2D NMR spectral data. The results clearly indicate that the compounds ex

Complete 1H and 13C NMR spectral assignm
✍ Cláudia J. Nascimento; Elizabete R. Cruz; J. Daniel Figueroa-Villar 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 91 KB 👁 1 views

Unambiguous 1H and 13C chemical shift assignments of the novel antibiotic 6,7,8,9-tetrahydro-7,7dimethyl-dioxolo [5,4-b]acridin-9-one were made using the FUCOUP pulse sequence. The appropriate phase cycling was calculated using the Compact Cartesian Coordinate Product Operator (C3PO) method. Copyrig

Assigned cluster 11B and 1H NMR properti
✍ Mark Bown; Jaromír Plešek; Karel Baše; Bohumil Štíbr; Xavier L. R. Fontaine; Nor 📂 Article 📅 1989 🏛 John Wiley and Sons 🌐 English ⚖ 286 KB

The cluster "B chemical shifts in members of the important class of closo-3,1,2-metalladicarbaboranes were previously unassigned, and their cluster 'H chemical shifts previously unmeasured. The use of 1' 'B-' 'BJ-COSY and 'H-{"B} NMR spectroscopy to measure and assign the cluster "B and 'H chemical