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Cross-Aldol Reaction (cross-aldol + reaction)

Distribution by Scientific Domains
Chemistry100%

Selected Abstracts

ChemInform Abstract: Asymmetric Bisprolinamide-Catalyzed Cross-Aldol Reaction of Aldehydes

CHEMINFORM, Issue 22 2008
Yan Xiong
Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a "Full Text" option. The original article is trackable via the "References" option. [source]

Germanium(II)-Mediated Reductive Cross-Aldol Reaction of Aldehydes: Synthesis of Aldols with Diastereocontrolled Quaternary Carbon Centers.

CHEMINFORM, Issue 44 2007
Shin-ya Tanaka
Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF. [source]

Combined Proline,Surfactant Organocatalyst for the Highly Diastereo- and Enantioselective Aqueous Direct Cross-Aldol Reaction of Aldehydes.

CHEMINFORM, Issue 50 2006
Yujiro Hayashi
Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF. [source]

The First Direct and Enantioselective Cross-Aldol Reaction of Aldehydes.

CHEMINFORM, Issue 42 2002
Alan B. Northrup
Abstract For Abstract see ChemInform Abstract in Full Text. [source]

ChemInform Abstract: A Designer Axially Chiral Amino Sulfonamide as an Efficient Organocatalyst for Direct Asymmetric anti-Selective Mannich Reactions and syn-Selective Cross-Aldol Reactions.

CHEMINFORM, Issue 46 2009
Taichi Kano
Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a "Full Text" option. The original article is trackable via the "References" option. [source]

Efficient, Enantioselective Organocatalytic Synthesis of Trichostatin A

ADVANCED SYNTHESIS & CATALYSIS (PREVIOUSLY: JOURNAL FUER PRAKTISCHE CHEMIE), Issue 10-11 2006
Shilei Zhang
Abstract An efficient, highly stereocontrolled total synthesis of trichostatin A (1) has been achieved in 9 steps with 17.4,% overall yield and >99,% optical purity from readily available achiral starting materials. The key features of this synthesis include the L -proline-promoted, highly enantioselective cross-aldol reaction as a crucial step for the construction of the C-6 chiral center and the minimization of racemization by final step oxidation of the OH group to a ketone at position 7. [source]