- stereospecific synthesis
-
a) The synthesis of a specific, chosen stereoisomerb) The synthesis of a stereospecific polymer
Wikipedia foundation.
stereospecific synthesis
Look at other dictionaries:
Carbohydrate synthesis — is a sub field of organic chemistry concerned specifically with the generation of natural and unnatural carbohydrate structures. This can include the synthesis of monosaccharide residues or structures containing more than one monosaccharide,… … Wikipedia
asymmetric synthesis — Chemical reaction by which unequal amounts of two product isomers are formed. It is normally not possible to synthesize from materials that do not have optical activity (i.e., are not chiral) one stereoisomer of a chiral compound without the… … Universalium
Oxaziridine — Oxaziridine … Wikipedia
Wittig reaction — The Wittig reaction is a chemical reaction of an aldehyde or ketone with a triphenyl phosphonium ylide (often called a Wittig reagent) to give an alkene and triphenylphosphine oxide. [cite journal author = Georg Wittig, Ulrich Schöllkopf journal … Wikipedia
Robert Burns Woodward — Infobox Scientist name = Robert Burns Woodward image width = caption = birth date = birth date|1917|4|10|mf=y birth place = Boston, Massachusetts death date = death date and age|1979|7|8|1917|4|10 death place = Cambridge, Massachusetts residence … Wikipedia
Tetrodotoxin — Chembox new ImageFile=Tetrodotoxin 2D skeletal.png ImageSize= ImageFile2=Tetrodotoxin 3D balls.png IUPACName=Octahydro 12 (hydroxymethyl) 2 imino 5,9:7,10a dimethano 10aH [1,3] dioxocino [6,5 d] pyrimidine 4,7,10,11,12 pentol… … Wikipedia
Methanesulfonyl chloride — Methanesulfonyl chloride … Wikipedia
Olivetol — IUPAC name 5 Pentyl 1,3 benzenediol … Wikipedia
Briserin — Strukturformel Allgemeines Freiname Reserpin Andere Namen (1S,2R … Deutsch Wikipedia
Briserin N — Strukturformel Allgemeines Freiname Reserpin Andere Namen (1S,2R … Deutsch Wikipedia
