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Angewandte Chemie (International ed.), ISSN 1433-7851, 12/2017, Volume 56, Issue 50, pp. 15989 - 15992
A new method for the iodine‐catalyzed reduction of phosphine oxides with phosphites at room temperature is reported. The mild reaction conditions, scalability,... 
phosphines | phosphine oxides | iodine | phosphites | reduction | REAGENT | DIIODINE | TRIPHENYLPHOSPHINE | CHEMISTRY, MULTIDISCIPLINARY | DENSITY FUNCTIONALS | PHOSPHONATE | TERTIARY PHOSPHINE | DEOXYGENATION | DERIVATIVES | Oxides | Temperature requirements | Regeneration | Reduction | Purification | Phosphine | Oxygen transfer | Phosphorus | Inorganic salts | Phosphine oxide | Phosphines | Iodine
Journal Article
Science (American Association for the Advancement of Science), ISSN 1095-9203, 2019, Volume 365, Issue 6456, pp. 910 - 914
Nucleophilic substitution reactions of alcohols are among the most fundamental and strategically important transformations in organic chemistry. For over half... 
SECONDARY ALCOHOLS | MILD | HYDROXYL-GROUPS | ACID | REDUCTION | MULTIDISCIPLINARY SCIENCES | NUCLEOPHILIC-SUBSTITUTION | ENONES | CATALYTIC WITTIG | PHOSPHINE OXIDES | GREEN | Substitution reactions | Catalysis | Chemical tests and reagents | Chemical synthesis | Alcohols | Oxygen | Phosphine | Byproducts | Phosphorus | Alcohol | Carbon | Phosphine oxide | Organic chemistry | Valence | Reagents | Phenols | Oxidation
Journal Article
Chemistry : a European journal, ISSN 0947-6539, 11/2017, Volume 23, Issue 61, pp. 15238 - 15243
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 2018, Volume 57, Issue 6, pp. 1702 - 1706
Journal Article
Synthesis (Stuttgart), ISSN 1437-210X, 2017, Volume 49, Issue 21, pp. 4783 - 4807
Abstract Traditional methods for C–P bond formation via direct addition of P–H species to unsaturated compounds are usually implemented in the presence of base... 
short review | phosphine oxides | phosphine sulfides | hydrophosphination | catalyst-free | phosphine selenides | hydrophosphinylation | solvent-free | green chemistry | APOPTOSIS | YTTERBIUM COMPLEXES | SULFIDES | CHEMISTRY, ORGANIC | TERTIARY | SECONDARY PHOSPHINE CHALCOGENIDES | LIGANDS | CLUSTERS | INTERMOLECULAR HYDROPHOSPHINATION | OXIDES | ACCESS
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 2014, Volume 53, Issue 29, pp. 7589 - 7593
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 10/2015, Volume 54, Issue 44, pp. 13041 - 13044
The Mitsunobu reaction is renowned for its mild reaction conditions and broad substrate tolerance, but has limited utility in process chemistry and industrial... 
organocatalysis | silanes | reaction kinetics | phosphorus heterocycles | synthetic methods | REDUCTION | DIETHYL AZODICARBOXYLATE | PHOSPHORIC-ACID | ESTERS | CHEMISTRY, MULTIDISCIPLINARY | Substitution reactions | Catalysis | Chemical reaction, Rate of | Chemical tests and reagents | Silane | Hydrazines | Purification | Catalysts | Byproducts | Tolerances | Phosphine oxide | Phosphines | Communications
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 2018, Volume 57, Issue 48, pp. 15877 - 15881
The first catalytic enantioselective aldol reaction of various unprotected carboxylic acids is described. In the presence of a chiral bis(phosphine oxide) as a... 
organocatalysis | phosphine oxides | aldol reaction | hypervalent silicon | carboxylic acids | REAGENT | CONSTRUCTION | ENOLBORATION | ADDITIONS | ANTI | CHEMISTRY, MULTIDISCIPLINARY | Oxides | Catalysis | Enantiomers | Organic acids | Silicon tetrachloride | Acids | Phosphine | Carboxylic acids | Lewis base | Aldehydes | Phosphine oxide
Journal Article