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11
Experimental and modeling study of liquid phase equilibria for (water phosphoric acid
sec
-
alcohols
) systems
.pdf
Experimental and modeling study of liquid phase equilibria for (water phosphoric acid sec-alcohols) systems
30caf8ddcb
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4
a stereoselective but inverting
sec
-alkylsulfatase for the deracemization of
sec
-
alcohols
.pdf
a stereoselective but inverting sec-alkylsulfatase for the deracemization of sec-alcohols
dashadonghui
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4
one-pot enzymatic resolution and separation of
sec
-
alcohols
based on ionic acylating agents
.pdf
one-pot enzymatic resolution and separation of sec-alcohols based on ionic acylating agents
touxavn7
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jbavun36g
one-pot enzymatic resolution and separation of sec-alcohols based on..
3
one-pot deracemization of
sec
-
alcohols
enantioconvergent enzymatic hydrolysis of alkyl sulfates using stereocomplementary sulfatases
.pdf
one-pot deracemization of sec-alcohols enantioconvergent enzymatic hydrolysis of alkyl sulfates using stereocomplementary sulfatases
ssweedtg6797
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4
kinetic resolution of
sec
-
alcohols
by a new class of pyridine catalysts having a conformation switch system
.pdf
kinetic resolution of sec-alcohols by a new class of pyridine catalysts having a conformation switch system
ac21836
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5
combinatorial library based engineering of candida antarctica lipase x2005;a for enantioselective transacylation of
sec
-
alcohols
in organic solvent
.pdf
combinatorial library based engineering of candida antarctica lipase
dkavlrs7m
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6
artificial multi-enzyme networks for the asymmetric amination of
sec
-
alcohols
.pdf
artificial multi-enzyme networks for the asymmetric amination of sec-alcohols
wmd58vasr
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5
biocatalytic enantio-convergent preparation of
sec
-
alcohols
using sulfatases
.pdf
biocatalytic enantio-convergent preparation of sec-alcohols using sulfatases
q32vh4a8f
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11
alcohols
_IPdoc -
sec
4 chistry-pehyk
.doc
alcohols_IPdoc - sec 4 chistry-pehyksec,sec4,SEC4
文档下单
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14
ial waste materials, 11. synthesis of new, chiral β-
sec
-amino
alcohols
- diastereodivergent addition of grignard reagents to α-amino aldehydes based on the (all-r)-2-azabicyclo[3.3..
.pdf
ial waste materials, 11. synthesis of new, chiral β-sec-amino alcohols - diastereodivergent addition of grignard reagents to α-amino aldehydes based on the (all-r)-2-azabicyclo[3.3.0]octane system
yu6seqo8b
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