Enantioselective synthesis of spirocyclic aminochroman derivatives according to the CN (R, S) strategy

G Pavé, JM Léger, C Jarry…

Index: Journal of Organic Chemistry, , vol. 68, # 4 p. 1401 - 1408

Full Text: HTML

Citation Number: 16

Abstract

... The Journal of Organic Chemistry. ... Indeed, the H-2b signal was inferred by the Karplus theory: H-2a, δ 3.55 (dd, J cis = 3.8 Hz, J gem = 11.0 Hz); H-2b, δ 4.28 (t, J trans = 11.0 Hz, J gem = 11.0 Hz); H-3, δ 3.93 (dd, J cis = 3.8 Hz, J trans = 11.0 Hz). ...

Related Articles:

Enantioselective synthesis of spirocyclic aminochroman derivatives according to the CN (R, S) strategy

[Pave, Gregoire; Leger, Jean-Michel; Jarry, Christian; Viaud-Massuard, Marie-Claude; Guillaumet, Gerald Journal of Organic Chemistry, 2003 , vol. 68, # 4 p. 1401 - 1408]

Synthesis of Concave 1, 10??Phenanthrolines by a Combination of Suzuki Coupling, Ring Closing Metathesis and Hydrogenation

[Luening, Ulrich; Fahrenkrug, Frank European Journal of Organic Chemistry, 2004 , # 14 p. 3119 - 3127]

The regioselective synthesis of halophenols

[Tetrahedron, , vol. 51, # 15 p. 4291 - 4296]

The regioselective synthesis of halophenols

[Tetrahedron, , vol. 51, # 15 p. 4291 - 4296]

More Articles...