Vmylacetylene 1 undergoes reactions with dienopNles by a mechanism involving initial addition of acids to the triple bond, cycloaddition, and elimination of add. For more than half a century the fact that vinylacetylenes can undergo cycloaddition reaclions with dienophiles ("dehydro Die&Alder reacti
An elimination-addition mechanism for some phosphonamidic chloride-amine reactions
✍ Scribed by Martin J.P. Harger
- Publisher
- Elsevier Science
- Year
- 1981
- Tongue
- French
- Weight
- 164 KB
- Volume
- 22
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
For the reactions of RPtOl(flHBut)Cl with PrtNH and ButNHz in CHy222, relative rates and product ratios suggest an eliminatiokaddition mechanism with a reartive fmonomerici metaphosphonimidate intermediate.
📜 SIMILAR VOLUMES
## Abstract Several intermediates for the CH~3~SH + OH^•^ → CH~3~S^•^ + H~2~O reaction were identified using MP2(full) 6‐311+g(2df,p) __ab initio__ calculations. An adduct, CH~3~S(H)OH^•^, I, with electronic energy 13.63 kJ mol^−1^ lower than the reactants, and a transition state, II^‡^, located 5.
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v