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N-(1-methyl)cyclopropylbenzylamine

Known as: N-cyclopropyl-alpha-methylbenzylamine, NMCPBA, alpha-methyl-N-cyclopropylbenzylamine 
National Institutes of Health

Papers overview

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Highly Cited
2013
Highly Cited
2013
Regioselective ring expansion of alkynyl cyclopropanes to highly substituted cyclobutenes was developed. The reaction involves a… 
2013
2013
Naturally occurring indole-3-carbinol and 3,3-diindolylmethane show bioactivity in a number of disparate disease areas, including… 
Review
2009
Review
2009
Abstract: Activated cyclopropanes, such as vinyl and carbonyl cyclopropanes, are useful building blocks in organic chemistry due… 
Highly Cited
2008
Highly Cited
2008
The cytochrome P540 (CYP) superfamily currently includes about 9,000 proteins forming more than 800 families. The enzymes… 
Highly Cited
2008
Highly Cited
2008
An efficient synthetic route to pyrrolidines that relies on AuCl/AgOTf-catalyzed tandem amination/ring expansion of substituted… 
Highly Cited
2004
Highly Cited
2004
The present study investigates the effect of varying ligand structure on the ability of agonists to activate guanine nucleotide… 
Highly Cited
2004
Highly Cited
2004
The homoallyl cation formed from a cyclopropyl carbinol that was vicinally substituted by a silylmethyl function underwent smooth… 
Highly Cited
2001
Highly Cited
2001
Efficient access to tricyclic compounds such as 2 and 3, which contain a seven-membered ring, is provided by the ruthenium… 
Highly Cited
1983
Highly Cited
1983
Adenosine receptors on the surface of coronary myocytes initiate coronary relaxation, but events subsequent to receptor occupancy…