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Addition of bromine to 2-methyl-2-azabicyclo[2.2.1]hept-5-ene

✍ Scribed by M. N. Bulanov; S. E. Sosonyuk; N. V. Zyk

Book ID
110300139
Publisher
Springer
Year
2001
Tongue
English
Weight
228 KB
Volume
50
Category
Article
ISSN
1573-9171

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πŸ“œ SIMILAR VOLUMES

ChemInform Abstract: Addition of Bromine
ChemInform Abstract: Addition of Bromine to 2-Methyl-2-azabicyclo[2.2.1]hept-5-ene.
✍ M. N. Bulanov; S. E. Sosonyuk; N. V. Zyk πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 26 KB πŸ‘ 1 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 β€œFull Text” option. The original article is trackable v

Absolute Configuration of 2-Substituted
Absolute Configuration of 2-Substituted 2-Azabicyclo[2.2.1]hept-5-enes
✍ Esteban Pombo-Villar; Jakob Boelsterli; Maria Magdalena Cid; Julien France; Beat πŸ“‚ Article πŸ“… 1993 πŸ› John Wiley and Sons 🌐 German βš– 781 KB

To avoid confusion, it is emphasised that ul and lk refer to additions to a particular face of the corresponding methaniminium ion. Thus, for discussion of the stereoselectivity of this reaction, we shall refer to relative topicity of the addition, rather than to the relative topicity of the product

Ring opening metathesis polymerization o
Ring opening metathesis polymerization of methyl-N-(1-phenylethyl)-2-azabicyclo[2.2.1]hept-5-ene-3-carboxylate
✍ Regina M.E Schitter; Thomas SteinhΓ€usler; Franz Stelzer πŸ“‚ Article πŸ“… 1997 πŸ› Elsevier Science 🌐 English βš– 858 KB

Enantiomerically pure (1) and rucemic (2) methyl-N-( 1-phenylethyl)-2-azabicycld2.2.1 lhept-5-ene-3-carboxylate were found to undergo ring opening metathesis polymerization reactions employing molybdenum alkylidene initiators of the type Mo(CH-t-Bu)(NArXOR), (Ar = 2,6-C,Ha-i-Pr2; R = C(CH,),; C(CH,)