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Addition of Azaenolates to Simple, Unactivated Olefins

✍ Scribed by Dr. Katsumi Kubota; Prof. Eiichi Nakamura

Publisher
John Wiley and Sons
Year
1997
Tongue
English
Weight
348 KB
Volume
36
Category
Article
ISSN
0044-8249

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πŸ“œ SIMILAR VOLUMES

ChemInform Abstract: Addition of Azaenol
ChemInform Abstract: Addition of Azaenolates to Simple, Unactivated Olefins.
✍ K. KUBOTA; E. NAKAMURA πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 35 KB

Addition of Azaenolates to Simple, Unactivated Olefins. -The title reaction provides ketone derivatives by an one-pot, three component (zinc hydrazone, olefin, electrophile) coupling as an olefinic analogue of the aldol reaction. -(KUBOTA, K.;

Oxidative Addition of the Azide Ion to O
Oxidative Addition of the Azide Ion to Olefins. A Simple Route to Diamines
✍ Dr. H. SchΓ€fer πŸ“‚ Article πŸ“… 1970 πŸ› John Wiley and Sons 🌐 English βš– 227 KB πŸ‘ 2 views

tations, while those with inorganic electron acceptors (except 0 2 ) are described as anaerobic respiration. Respiration occurs when oxygen acts as the terminal oxidant. Terms such as "fumarate respiration" and "inorganic fermentation" are incompatible with this view. A self-consistent definition o

ChemInform Abstract: Facile Addition of
ChemInform Abstract: Facile Addition of Poorly Nucleophilic Alcohols to Unactivated Alkenes.
✍ D. F. SHELLHAMER; R. P. CALLAHAN; V. L. HEASLEY; M. L. DRUELINGER; R. D. CHAPMAN πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 31 KB

Facile Addition of Poorly Nucleophilic Alcohols to Unactivated Alkenes. -Strongly electronegatively substituted poorly nucleophilic alocohols (II) and (V) undergo efficient addition reactions to unactivated alkenes using BF 3 -etherate as catalyst.