153141-25-4

Upstream product

• 34446-64-5 (E)-3-(4-methoxyphenyl)propenoyl chloride 
• 94594-90-8 (2R)-bornane-10,2-sultam 

Downstream Products

• 1392445-70-3 C₁₃H₁₆N₂O₂ 
• 1092461-45-4 N-[(3R)-3-(4-methoxyphenyl)pentanoyl]bornane-10,2-sultam 
• 1357375-10-0 (3R)-3-(4-methoxyphenyl)-4-nitro-1-[ (3aS,6R,7aR)tetrahydro-8,8-dimethyl-2,2-dioxido-3H-3a,6-methano-2,1-benzisothiazol-1(4H)-yl]butan-1-one 
• 153141-37-8 (R)-3-(Dimethyl-phenyl-silanyl)-3-(4-methoxy-phenyl)-propionic acid 
• 153141-38-9 (R)-3-(4-Chloro-phenyl)-3-(dimethyl-phenyl-silanyl)-propionic acid 
• 122517-81-1 (2R,3S)-methyl 2,3-dihydroxy-3-(4-methoxyphenyl)propanoate 
• 943-89-5 (E)-3-(4-methoxyphenyl)acrylic acid 
• 153141-33-4 (R)-1-((1S,5R,7R)-10,10-Dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]dec-4-yl)-3-(dimethyl-phenyl-silanyl)-3-(4-methoxy-phenyl)-propan-1-one 

Relevant academic research and scientific papers

Asymmetric syn-Dihydroxylation of β-Substituted (2R)-N-(α,β-Enoyl)bornane-10,2-sultams

Variously β-substituted (2R)-N-[(E)-α,β-enoyl]bornane-10,2-sultams were oxidized with OsO4/4-methylmorpholine 4-oxide in a highly stereoselective manner. In all cases, the attack occurred on the C(α)-re face. The absolute configurations of all

Grignard 1,4-Additions to para-Substituted (2R)-N-Cinnamoylbornane-10,2-sultam Derivatives: Revised Configuration for the N,OAc-Keteneacetal Formation in the Presence of Cu(I)

Using a19F-NMR analytical method, we have corrected and improved the linear correlation initially found between the diastereoselectivity observed during the EtMgBr conjugated addition to Michael acceptors of type 1, as a function of their σsub

Diastereoselective alkyl Grignard 1,4-additions to para-substituted (2R)-N-cinnamoylbornane-10,2-sultam derivatives: Influence of N-atom pyramidalization

Several typical 13C-NMR displacements (of C=O, C(α), C(β), and Cipso), as well as conformational or energy properties (S-N-C=O dihedral angle, ΔE syn/anti; HOMO/LUMO) could be correlated with the electronic parameters of p-substitute