𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Note on the Direct α-Phenylsulfenylation of Enolates Generated During 1, 4-Addition Reactions on α, β-Unsaturated Ketones

✍ Scribed by M. Samson; H. De Wilde; M. Vandewalle


Publisher
Wiley (John Wiley & Sons)
Year
2010
Weight
101 KB
Volume
86
Category
Article
ISSN
0037-9646

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Influence of enolate geometry on the ste
✍ David A Oare; Clayton H Heathcock 📂 Article 📅 1986 🏛 Elsevier Science 🌐 French ⚖ 207 KB

Preformed lithium enolates of ketones react with acyclic a,p-unsaturated ketones to give 1,5-diketones in good chemical yields. A strong correlation exists between enolate geometry and product stereochemistry; enolates having the z configuration provide anti addition products while E enolates usua

ChemInform Abstract: Steric and Complexa
✍ A. S. VELLEKOOP; R. A. J. SMITH 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 35 KB 👁 2 views

## 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

A selective synthesis of 3-alkynl perflo
✍ Ei-ichi Takada; Shoji Hara; Akira Suzuki 📂 Article 📅 1992 🏛 John Wiley and Sons 🌐 English ⚖ 323 KB

A variet-y of3-alkynyl perfluoroaikyi ketones were prepared by a trifluoroborane etherate mediated 1,4-addition reaction of ( I -alkynyl)diisopropoxyboranes to a,p-unsaturated ketones substituted by a perfltloroalkyl group. The undesired side reaction, such as 1,2-addition of alkynyl groups, could b