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Asymmetric Synthesis, Partial and Absolute With Examples

1. Asymmetric synthesis involves synthesizing a chiral compound from an achiral starting material using a chiral catalyst or reagent, yielding diastereomeric or enantiomeric products in unequal amounts. 2. There are several methods for asymmetric synthesis, including substrate-controlled reactions, use of chiral auxiliaries, and use of chiral reagents or catalysts. 3. Examples are provided for each type of asymmetric synthesis, such as the reduction of pyruvic acid to lactic acid using yeast or the formation of lactic acid from pyruvic acid with a chiral auxiliary.

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Usama Khalil
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100% found this document useful (2 votes)
2K views

Asymmetric Synthesis, Partial and Absolute With Examples

1. Asymmetric synthesis involves synthesizing a chiral compound from an achiral starting material using a chiral catalyst or reagent, yielding diastereomeric or enantiomeric products in unequal amounts. 2. There are several methods for asymmetric synthesis, including substrate-controlled reactions, use of chiral auxiliaries, and use of chiral reagents or catalysts. 3. Examples are provided for each type of asymmetric synthesis, such as the reduction of pyruvic acid to lactic acid using yeast or the formation of lactic acid from pyruvic acid with a chiral auxiliary.

Uploaded by

Usama Khalil
Copyright
© © All Rights Reserved
Available Formats
Download as PDF, TXT or read online on Scribd
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Pheym Og Chum-1

Asymmeric Synthesis
Parttal and Abaolute Aaymvehric Synthesis Dr. Parjanya Shukla
&
Dr. M. P. Singh Ctassets
When a asyoMMetii Compomel Coithciya lrben) ipb
Synthasi2td by a Byommehic compoomed im movmal Coreliban
the pduct is q aemic mixure

1Auth a Aynthesis iS Ceriad undar csymmetic


inuente Ceithar ophtally acrive rraenh catalyst et), Only
one anamtioaY in dermucl Ceithur 4) o rE)) .

his mum In vohich an asymmtieCwmpoumod s


synthasized y o m m e t m c Compoumal o yielel t)isomuY
aY somer oindly l Lallud Aymmtric ynthsis
3Dr ngmya kr Shukla
ExoAmpl Racluhion af eyruvic atid with HINi ive
acemiC mixtue t ) lache acid
But o h n pyruvic acid rduud by east er im
it ives omly )leche
Lym Leachc atid cuhyehvgenaS
acic
CH CHa
HN H-CoH OH-¢TH ordipy
CH CoOH Synthas
Lach' c qud ) Lachiequd
CODH

youvic aid Racamic MixBure


Syrmmtmal
CoMpoyd CH Omly one 2YomomY

oithout chiral yeast H-COH


Lachcauid Hssumonetme
COOH sumthasis
dohydongorask
(G-lachcqu
Asymetric Aynthasis is dlainal as. ComyeTbion of anachia
Coymmetial) Compormd into q chiral (Asyonmetial) Compoumd
in puch a oay that both erantiomeYs deml in unequo
Mounts?
his tpe oreachions done undar tha
intuanus
of o m chira agent, chiral solvant or catalyopt
pesonu ch rularly polenised light at. Dr. Parjanya Shukla

Dr. M.P. Singh


hese racios darms stureoisomeic (enmtiouanic Clases
c
diastrmomeric) prvelucts în umequal aMounts
Amyomatre symthaois Con be of tuoo types
B
A) arviad asymmetic synthabis Dr.Varganya kr Shukla
Aboolurr aymmtrc ynthasis.
A) Vontial avsyomnmaie Aunthub}a It Con b dogind as
ynthesis of a na chial
Caynter oom an achira Canter by using ophically achive
Laents or Codalysts or solvets etn.

Methods f Pavmad asummehic Aynthaois


D Hrst gwration or
Aubstrate controllad asymnehric upthuis
n this Method ha subtotrate id usually a pume enantiomur
omaturad ogin A nauo chiral Center a t dermd
under the imfuenu a host alhtady presint

Eyarmple hycwboration ot )-isopulagol , new chirol anter


dovm amady prestnt chiral cor quiela th
atac o hyehoboopn doom the reorc moletule
H H
H,THA
H
o'C
H HO
HO
HO H NaOHH

HO H Ne
-CH H
H 3 Cayh
Chira

-isopudagol
TR,2s,s R
H-B
H
OH

(-)elarivative(a)
Irenneeliota) Nw chhral hae
S Cenqusattom
2 Secorel-geneyatiom Methods. Use of chiral auxiliades.
Dr. Parjanya Shukla

hese veactioms conollud by auxilay uwhieh Dr. M.P. Singh Clases


r e chira molatuly ( ovicle. aobli tom Aupprt).

In thuse ynthsis chirality is intrducal by tha attachunant


a a chira quxilary (suppert) uoich dlincs tha
ntiou
Aubegusnt actom Jor the dTmotiom o one
A}tr Cornplating octiem auriloy jirmlly ovecl

Exruplefomotion of lachicacil M pyuvic auid oith


the halp of e mnthol las chiral auxieny)

OH sstianen
HO H
Pynuvic aid --Manthol Munthy pyruvate
(Symnehric) Cauxi ory)
H2/Ni
Nao chiral Aacluehion
OH
on HHo
bH
HO
+ 2Movo
auxilou4 meythy loctate
Elachic aud -Manthe
ryomnetme) 5 r-lonmamya rShukla
3) 3 qcrncrorion Methors Use o chial Vtagents
which
In a chirad pwcuct Jormaal diety by treating
am achiral Atartin compoumal usith a chiral 7ogenk
oith iAlHy in nsone
Exomplk Realuchion) a povpiophenone
ot pooli-cerivec oiamine gives S-l- phanyl povpon-l-ol.
Ho .H
+ HN
LiA CH GHs Dr. Parjanya Shukla
Dr. M. P.
Singh Classes
Poppiophenone Sl-phavng-prpan-
-ol
Achirod)
(SynonehMc)
chiral 30%) Chiral Compownel)
Raogen) (Pymehie)

)uthgenrariom Methools Use d Chiral catalysts!


Extensiom of 3agsoriom) uohare actiom is infmntael
in the PMSnLa o a chia CatalysF
n3yma-Catalyed achem baloneys to this cluss

ExaMpl Convavbim o E) Lache que m pyuvicaud


by
b oubt r lachc aud olahuchrogenas anzy
e n 15 Pag)
B) Absolute Asummnerie Synthasis: Ih is the syrthasis
ot optoally acive
roclucs oDM achirad ulstoate oithout u d of amy
opticoly achve chamicals (no>agimk catalyot olvent et)
In thuid type o Aythesis a physical presena f chiaiy
Like Ciulatry poloiscol light s netasenry.

Exampla Acdolihon o broomin to 2,4,6 timitoshlbora aive


daxtotatuyy moluct by th uscdl oh Cruletny
polavisee light Cfar tha imduetin of chiality)
Neo chira
NO HH
NOCH=CH- CPL
lo, 3 Br
NO
Syonmede Aubstrate ison
No chial Certuy
Dr errjomya Kr Shukla
Hoo.nt HOD
Krismspit ns.of Phamety
fny ara nodla

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