- In stereochemistry,
stereoisomerism, or
spatial isomerism, is a form of
isomerism in
which molecules have the same
molecular formula and
sequence of bonded...
- doi:10.1351/pac200678101897. S2CID 97528124.
IUPAC definition of "
stereoisomerism"
IUPAC definition of "geometric isomerism"
IUPAC definition of "cis–trans...
- a
molecule is an atom (center), axis or
plane that is the
focus of
stereoisomerism; that is, when
having at
least three different groups bound to the...
- In
organic chemistry, endo–exo
isomerism is a
special type of
stereoisomerism found in
organic compounds with a
substituent on a
bridged ring system....
- constitutional) isomerism, in
which bonds between the
atoms differ; and
stereoisomerism or (spatial isomerism), in
which the
bonds are the same but the relative...
-
Planar chirality, also
known as 2D chirality, is the
special case of
chirality for two dimensions. Most fundamentally,
planar chirality is a mathematical...
- administration.
Tramadol is
marketed as a
racemic mixture of both R- and S-
stereoisomers,
because the two
isomers complement each other's
analgesic activities...
-
effect Stereochemistry for
overview of
stereochemistry in
general Stereoisomerism Supramolecular chirality Organic Chemistry (4th Edition)
Paula Y. Bruice...
- doi:10.1351/goldbook.S05980 Mislow, Kurt; Siegel, Jay (1984). "
Stereoisomerism and
local chirality". J. Am. Chem. Soc. 106 (11): 3319–3328. doi:10...
- l-rotary,
represented by (−), counter-clockwise)
depending on
which stereoisomer is dominant. For instance,
sucrose and
camphor are d-rotary
whereas cholesterol...
