Results 231 to 240 of about 27,319 (289)

A Multicatalytic Cascade for the Stereoselective Synthesis of 1,4-Chiral Nitro Alcohols. [PDF]

Org Lett
Ascaso-Alegre C, Linacero-Gracia Á, Ferreira P, Herrera RP, Mangas-Sánchez J.   +4 more
europepmc   +1 more source

Stereoselective additions to alkenylphosphonium salts for the synthesis of P-stereogenic compounds. [PDF]

Chem Sci
Chen XB, Padín D, Feringa BL.
europepmc   +1 more source

Selective isomerization of 2,3-disubstituted butanediacetal esters and thioesters using lithium and sodium enolates: effects of bases and additives on stereoselectivity. [PDF]

Front Chem
Drop A, Grzegolec M, Frąckowiak-Wojtasek B.   +2 more
europepmc   +1 more source

Stereoselectivity and functional plasticity of a common ligand-binding pocket in TRPM3. [PDF]

Nat Commun
Bazeli B, Shkumatov AV, Schenck S, Vanherck JC, Janssens A, Spieser SAH, Marchand D, Roelens R, Chaltin P, Marchand A, Vriens J, Voets T, Brunner JD.   +12 more
europepmc   +1 more source

Selective and Tunable Routes for Glucose to Fructose Conversion Using MgCl₂ Catalysis and Comparison to Other Metal Ions. [PDF]

ChemistryOpen
Maragani R, Meier S.
europepmc   +1 more source

Some of the next articles are maybe not open access.

Related searches:

Stereoselective radical reactions

Chemical Society Reviews, 2003
AbstractFor Abstract see ChemInform Abstract in Full Text.
Gregory, Bar, Andrew F, Parsons
openaire   +2 more sources

Stereoselective Synthesis of (‐)‐Allosedamine.

ChemInform, 2004
Abstract A stereoselective synthesis of (−)-allosedamine is disclosed. β-Aminosulfoxide 4 was generated stereoselectively by condensation of the sulfinyl anion 2 with N-Ts imine 3 . The bromohydrin 5 was obtained by intramolecular sulfinyl group participation and the piperidine ring of allosedamine was elaborated using the ring-closing ...
Sadagopan Raghavan, A. Rajender
openaire   +1 more source

Stereoselective Synthesis of (+)-Boronolide

The Journal of Organic Chemistry, 2002
The delta-lactone boronolide (+)-1, a pharmacologically active, naturally occurring product, has been synthesized in enantiopure form with L-erythrulose as the chiral starting material. The key steps of the synthesis were a highly stereoselective aldol-reduction one-pot sequence, an indium-mediated diastereoselective aldehyde allylation, and a ring ...
Miguel, Carda, Santiago, Rodríguez, Beatriz, Segovia, J Alberto, Marco   +3 more
openaire   +2 more sources

Stereoselective synthesis of (+)-hyptolide

Tetrahedron Letters, 2003
Abstract The first total synthesis of the naturally occurring lactone (+)-hyptolide is described. Ethyl l -lactate was the chiral starting material. Key steps of this 15-step synthesis were a Brown's asymmetric allylation, a Carreira's asymmetric ethynylation and a ring closing metathesis.
Juan Murga, Jorge Garcia‐Fortanet, Miguel Carda, J. Alberto Marco   +3 more
openaire   +1 more source

Stereoselective Bromofunctionalization of Alkenes

Chirality, 2013
ABSTRACTThe stereoselective bromofunctionalization of alkenes, particularly the enantioselective format, has been a subject of intense research in recent years. The ground‐breaking works are documented in recent reviews. On the other hand, this account will provide an insight into our group's approach in tackling the challenges in enantioselective ...
Chong Kiat, Tan, Wesley Zongrong, Yu, Ying-Yeung, Yeung   +2 more
openaire   +2 more sources