𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Compounds with bridgehead nitrogen 68—NMR spectra and stereochemistry of perhydropyrido [1,2-c] [1,3]oxazines

✍ Scribed by Trevor A. Crabb; Simon T. Ingate; Thomas G. Nevell


Publisher
John Wiley and Sons
Year
1992
Tongue
English
Weight
238 KB
Volume
30
Category
Article
ISSN
0749-1581

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

Low‐temperature ^13^C NMR spectroscopy shows perhydropyrido [1,2‐c] [1,3]oxazine to adopt a conformational equilibrium in CD~2~Cl~2~–CFCl~3~ solution containing 98% trans fused conformer in equilibrium with 2% O‐outside‐cis fused conformer at 203 K. A similar equilibrium position is adopted by the trans‐(H‐4,H‐4a)‐4‐methylperhydropyrido[1,2‐c][1,3]oxazine, whereas the C‐4 epimer adopts exclusively the trans fused conformation.


📜 SIMILAR VOLUMES


Compounds with bridgehead nitrogen. 63—N
✍ Trevor A. Crabb; Asadollah Fallah 📂 Article 📅 1990 🏛 John Wiley and Sons 🌐 English ⚖ 417 KB

## Abstract The configurations and conformations of diastereoisomeric 1‐(decahydroquinolin‐8‐yl)butan‐2‐ols and of perhydropyrido[3,2,1‐__j,k__][3,1]benzoxazepines resulting from ring closure of these compounds with formaldehyde have been assigned by ^1^H and ^13^C NMR spectroscopy.

Compounds with bridgehead nitrogen 53—13
✍ Trevor A. Crabb; Olive G. Roch; Brian Wood 📂 Article 📅 1987 🏛 John Wiley and Sons 🌐 English ⚖ 337 KB

The configurations and preferred conformations of some diastereoisomeric perhydronaphthaleno[2,1-elpyrido[ 1,2c][ 1,310xazines have been assigned by "C NMR spectroscopy. These results require reversal of two previous tentative configurational assignments based on 'H NMR spectroscopy, and also indica

Compounds with bridgehead nitrogen. 40—S
✍ Trevor A. Crabb; Jacqueline S. Mitchell; Christopher H. Turner 📂 Article 📅 1981 🏛 John Wiley and Sons 🌐 English ⚖ 481 KB

## Abstract Seven of the possible diastereoisomeric perhydronaphthaleno[3,4‐__e__]pyrido[1,2‐__c__][1,3]oxazines have been synthesized and the configurations and preferred conformations of these assigned on the basis of IR and ^1^H NMR spectroscopy and the application of conformational principles.

Compounds with bridgehead nitrogen. 44—t
✍ Trevor A. Crabb; Philip A. Jupp; Yoshito Takeuchi 📂 Article 📅 1982 🏛 John Wiley and Sons 🌐 English ⚖ 270 KB

## Abstract The 270 MHz NMR data on __trans__‐ and __cis__‐(H‐4a, H‐7)‐7‐ethylperhydropyrido[1,2‐__c__][1,3]thiazine show heavy conformational bias to the __trans__‐ and __S__‐inside __cis__‐fused conformations, respectively. Comparison of the ^13^C NMR spectra of these anancomeric systems with the

Compounds with bridgehead nitrogen. Part
✍ Trevor A. Crabb; Simon T. Ingate; Thomas G. Nevell; Steven Sumner 📂 Article 📅 1993 🏛 John Wiley and Sons 🌐 English ⚖ 273 KB

## Abstract The positions of conformational equilibria in the four diastereoisomers of 8,9,11,11a,11b,12,13‐octahydro‐7a__H__‐quino [1,2‐__c__] [1,3] benzoxazines were investigated using ^13^C and ^1^H NMR spectroscopy. Comparison of the NMR chemical shifts of these isomers with those in the corres