Alcohol dehydrogenase catalysed reductions in non-conventional media:
Gespeichert in:
| 1. Verfasser: | |
|---|---|
| Format: | Elektronisch Software E-Book |
| Sprache: | English |
| Veröffentlicht: |
2004
|
| Ausgabe: | 1 CD-ROM ; 12 cm |
| Schlagworte: | |
| Online-Zugang: | Inhaltsverzeichnis |
| Beschreibung: | Rostock, Univ., Diss., 2004 |
| Beschreibung: | 1 CD-ROM 12 cm. - 12 cm Beil. (1 S.) |
Internformat
MARC
| LEADER | 00000nmm a2200000 c 4500 | ||
|---|---|---|---|
| 001 | BV019888173 | ||
| 003 | DE-604 | ||
| 006 | a m||| 00||| | ||
| 007 | co|uuu---uuuuu | ||
| 008 | 050718s2004 gw |||| q||u| ||||||eng d | ||
| 015 | |a 05,H06,1038 |2 dnb | ||
| 016 | 7 | |a 974501824 |2 DE-101 | |
| 035 | |a (OCoLC)634913196 | ||
| 035 | |a (DE-599)BVBBV019888173 | ||
| 040 | |a DE-604 |b ger |e rakddb | ||
| 041 | 0 | |a eng | |
| 044 | |a gw |c XA-DE | ||
| 049 | |a DE-355 | ||
| 084 | |a 540 |2 sdnb | ||
| 100 | 1 | |a Eckstein, Marrit Friederike |d 1976- |e Verfasser |0 (DE-588)129958921 |4 aut | |
| 245 | 1 | 0 | |a Alcohol dehydrogenase catalysed reductions in non-conventional media |c vorgelegt von Marrit Friederike Eckstein |
| 250 | |a 1 CD-ROM ; 12 cm | ||
| 264 | 1 | |c 2004 | |
| 300 | |a 1 CD-ROM |c 12 cm. - 12 cm |e Beil. (1 S.) | ||
| 336 | |b txt |2 rdacontent | ||
| 337 | |b c |2 rdamedia | ||
| 338 | |b cd |2 rdacarrier | ||
| 500 | |a Rostock, Univ., Diss., 2004 | ||
| 650 | 0 | 7 | |a Alkohole |g sekundär- |0 (DE-588)4343428-9 |2 gnd |9 rswk-swf |
| 650 | 0 | 7 | |a Lösungsmitteleffekt |0 (DE-588)4168032-7 |2 gnd |9 rswk-swf |
| 650 | 0 | 7 | |a Katalytische Aktivität |0 (DE-588)4279994-6 |2 gnd |9 rswk-swf |
| 650 | 0 | 7 | |a Alkoholdehydrogenasen |0 (DE-588)4285029-0 |2 gnd |9 rswk-swf |
| 650 | 0 | 7 | |a Ketone |0 (DE-588)4129416-6 |2 gnd |9 rswk-swf |
| 650 | 0 | 7 | |a Reduktion |g Chemie |0 (DE-588)4277879-7 |2 gnd |9 rswk-swf |
| 650 | 0 | 7 | |a Lactobacillus brevis |0 (DE-588)4166373-1 |2 gnd |9 rswk-swf |
| 650 | 0 | 7 | |a Enzymkatalyse |0 (DE-588)4152480-9 |2 gnd |9 rswk-swf |
| 650 | 0 | 7 | |a Prochiralität |0 (DE-588)4175781-6 |2 gnd |9 rswk-swf |
| 655 | 7 | |0 (DE-588)4113937-9 |a Hochschulschrift |2 gnd-content | |
| 689 | 0 | 0 | |a Ketone |0 (DE-588)4129416-6 |D s |
| 689 | 0 | 1 | |a Prochiralität |0 (DE-588)4175781-6 |D s |
| 689 | 0 | 2 | |a Reduktion |g Chemie |0 (DE-588)4277879-7 |D s |
| 689 | 0 | 3 | |a Enzymkatalyse |0 (DE-588)4152480-9 |D s |
| 689 | 0 | 4 | |a Alkoholdehydrogenasen |0 (DE-588)4285029-0 |D s |
| 689 | 0 | 5 | |a Alkohole |g sekundär- |0 (DE-588)4343428-9 |D s |
| 689 | 0 | |5 DE-604 | |
| 689 | 1 | 0 | |a Alkoholdehydrogenasen |0 (DE-588)4285029-0 |D s |
| 689 | 1 | 1 | |a Lactobacillus brevis |0 (DE-588)4166373-1 |D s |
| 689 | 1 | 2 | |a Reduktion |g Chemie |0 (DE-588)4277879-7 |D s |
| 689 | 1 | 3 | |a Katalytische Aktivität |0 (DE-588)4279994-6 |D s |
| 689 | 1 | 4 | |a Lösungsmitteleffekt |0 (DE-588)4168032-7 |D s |
| 689 | 1 | |5 DE-604 | |
| 856 | 4 | 2 | |m DNB Datenaustausch |q application/pdf |u http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=013212223&sequence=000001&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA |3 Inhaltsverzeichnis |
| 943 | 1 | |a oai:aleph.bib-bvb.de:BVB01-013212223 | |
Datensatz im Suchindex
| _version_ | 1808135125310898176 |
|---|---|
| adam_text |
INDEX
INDEX
1
INTRODUCTION
1
2
SCOPE
OF
THE
WORK
5
3
ENZYMES
IN
ORGANIC
SYNTHESIS
7
3.1
ENZYMES
UNDER
NON-CONVENTLONAL
CONDITIONS
7
3.2
SYNTHESIS
OF
ENANTIOPURE
ALCOHOLS
11
4
ALCOHOL
DEHYDROGENASES
15
4.1
COFACTOR
REGENERATION
15
4.2
ALCOHOL
DEHYDROGENASES
FOR
ENANTIOSELECTIVE
SYNTHESIS
19
4.3
ALCOHOL
DEHYDROGENASE
FROM
LACTOBACILLUS
BREVIS
(LB-ADH)
21
5
RESULTS
AND
DISCUSSION
-
PART
I
25
5.1
REDUCTIONS
IN
ONE
-
PHASE
SYSTEMS
-
ADDITION
OF
CO-SOLVENTS
26
5.1.1
WATER
ACTIVITY
OF
BUFFER
-
SOLVENT
MIXTURES
27
5.1.2
INFLUENCE
OF
THE
BUFFER
-
SOLVENT
MIXTURE
ON
LB-ADH
ACTIVITY
28
5.1.3
KINETIC
BEHAVIOUR
OF
LB-ADH
IN
THE
PRESENCE
OF
ACETONITRILE
29
5.1.4
INFLUENCE
OF
THE
BUFFER
-
SOLVENT
MIXTURE
ON
K
M
30
5.2
REDUCTIONS
IN
TWO
-
PHASE
SYSTEMS
34
5.2.1
PARTITION
COEFFICIENTS
35
5.2.2
KINETIC
BEHAVIOUR
OF
LB-ADH
IN
TWO-PHASE
SYSTEMS
39
5.3
REDUCTIONS
WITH
IMMOBILISED
LB-ADH
IN
ORGANIC
SOLVENTS
44
5.3.1
INFLUENCE
OF
WATER
ACTIVITY
AND
SOLVENT
46
5.3.2
KINETIC
BEHAVIOUR
OF
IMMOBILISED
LB-ADH
IN
ORGANIC
SOLVENTS
47
5.4
PREDICTION
OF
EQUILIBRIUM
CONVERSIONS
49
5.4.1
EQUILIBRIUM
CONVERSION
IN
ONE-PHASE
SYSTEMS
51
5.4.2
EQUILIBRIUM
CONVERSION
IN
TWO-PHASE
SYSTEMS
53
5.4.3
EQUILIBRIUM
CONVERSION
-
IMMOBILISED
LB-ADH
55
5.5
WHICH
IS
THE
SUITABLE
REACTION
MEDIUM
FOR
SYNTHESIS?
57
5.6
INTERIMS
SUMMARY
59
6
RESULTS
AND
DISCUSSION
-
PART
II
61
6.1
CHOICE
OF
COFACTOR
REGENERATION
METHOD
61
6.1.1
COFACTOR
REGENERATION
USING
GLUCOSE
AND
PS-GDH
'
63
6.2
SYNTHESIS
OF
(R)-2-OCTANOL
-
LB-ADH
AND
PS-GDH
65
6.2.1
TEMPERATURE
AND
PH
PROFILE
FOR
LB-ADH,
PS-GDH
AND
COFACTOR
65
6.2.2
ENZYME
STABILITY
AND
INHIBITION
BEHAVIOUR
67
6.2.3
(R)-2-OCTANOL
-
PARAMETERS
FOR
SCALE-UP
69
6.3
SYNTHESIS
OF
(S)-2-OCTANOL
-
TS-ADH
AND
PS-GDH
74
6.3.1
TEMPERATURE
AND
PH
PROFILE
FOR
TS-ADH
AND
PS-GDH
74
6.3.2
INHIBITION
BEHAVIOUR
75
6.3.3
(S)-2-OCTANOL
-
PARAMETERS
FOR
SCALE-UP
76
6.4
ESTIMATION
OF
PROCESS
COSTS
79
II
INDEX
7
SUMMARY
83
8
OUTLOOK
85
9
MATERIALS
AND
METHODS
89
9.1
LIST
OF
MATERIALS
89
9.2
LIST
OF
CHEMICALS
90
9.3
ENZYME
ASSAYS
91
9.3.1
LB-ADH
91
9.3.2
TS-ADH
91
9.3.3
PS-GDH
92
9.4
METHODS
OF
ANALYSIS
93
9.4.1
GC-ANALYSIS
FOR
LIPASE-CATALYSED
KINETIC
RESOLUTION
93
9.4.2
GC-ANALYSIS
FOR
ADH-CATALYSED
REDUCTIONS
93
9.4.3
GC-ANALYSIS
OF
CHIRAL
ALCOHOLS
94
9.4.4
HPLC-ANALYSIS
OF
ACETONE
AND
2-PROPANOL
94
9.5
CALCULATION
OF
THE
CONVERSION
94
9.6
LIPASE
CATALYSED
KINETIC
RESOLUTION
OF
(R,S)-2-OCTANOL
95
9.7
REDUCTIONS
IN
BUFFER
-
SOLVENT
MIXTURES
95
9.8
REDUCTIONS
IN
TWO-PHASE
SYSTEMS
96
9.8.1
PARTITION
COEFFICIENTS
96
9.8.2
SUBSTRATE-COUPLED
COFACTOR
REGENERATION
97
9.8.3
ENZYME-COUPLED
COFACTOR
REGENERATION
98
9.9
REDUCTIONS
USING
IMMOBILISED
LB-ADH
99
9.9.1
IMMOBILISATION
OF
LB-ADH
ON
CELITE
56099
9.9.2
SUBSTRATE-COUPLED
COFACTOR
REGENERATION
99
9.10
REDUCTION
OF
2-OCTANONE
AT
PREPARATIVE
SCALE
100
9.10.1
TOTAL
REACTION
VOLUME
OF
125
ML
(LB-ADH
AND
TS-ADH)
100
9.10.2
TOTAL
REACTION
VOLUME
OF
1250
ML
(LB-ADH)
100
9.11
REDUCTION
OF
P-NITROACETOPHENONE
AT
PREPARATIVE
SCALE
101
10
LITERATURE
103
11
APPENDIX
115
11.1
CORRELATION
BETWEEN
VOLUME
PERCENT
%
(V/V)
AND
MOLE
FRACTION
X
115
11.2
WATER
ACTIVITY
OF
WATER-SOLVENT
M
IXTU
RES
115
11.3
INFLUENCE
OF
MIXING
SPEED
ON
INTERFACIAL
AREA
A
116
11.4
PARTITION
COEFFICIENTS
116
11.5
CHROMATOGRAMS
OF
ENANTIOPURE
(R)-2-OCTANOL
118 |
| any_adam_object | 1 |
| author | Eckstein, Marrit Friederike 1976- |
| author_GND | (DE-588)129958921 |
| author_facet | Eckstein, Marrit Friederike 1976- |
| author_role | aut |
| author_sort | Eckstein, Marrit Friederike 1976- |
| author_variant | m f e mf mfe |
| building | Verbundindex |
| bvnumber | BV019888173 |
| ctrlnum | (OCoLC)634913196 (DE-599)BVBBV019888173 |
| discipline | Chemie / Pharmazie |
| edition | 1 CD-ROM ; 12 cm |
| format | Electronic Software eBook |
| fullrecord | <?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>00000nmm a2200000 c 4500</leader><controlfield tag="001">BV019888173</controlfield><controlfield tag="003">DE-604</controlfield><controlfield tag="006">a m||| 00|||</controlfield><controlfield tag="007">co|uuu---uuuuu</controlfield><controlfield tag="008">050718s2004 gw |||| q||u| ||||||eng d</controlfield><datafield tag="015" ind1=" " ind2=" "><subfield code="a">05,H06,1038</subfield><subfield code="2">dnb</subfield></datafield><datafield tag="016" ind1="7" ind2=" "><subfield code="a">974501824</subfield><subfield code="2">DE-101</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(OCoLC)634913196</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-599)BVBBV019888173</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-604</subfield><subfield code="b">ger</subfield><subfield code="e">rakddb</subfield></datafield><datafield tag="041" ind1="0" ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="044" ind1=" " ind2=" "><subfield code="a">gw</subfield><subfield code="c">XA-DE</subfield></datafield><datafield tag="049" ind1=" " ind2=" "><subfield code="a">DE-355</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">540</subfield><subfield code="2">sdnb</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Eckstein, Marrit Friederike</subfield><subfield code="d">1976-</subfield><subfield code="e">Verfasser</subfield><subfield code="0">(DE-588)129958921</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Alcohol dehydrogenase catalysed reductions in non-conventional media</subfield><subfield code="c">vorgelegt von Marrit Friederike Eckstein</subfield></datafield><datafield tag="250" ind1=" " ind2=" "><subfield code="a">1 CD-ROM ; 12 cm</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2004</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">1 CD-ROM</subfield><subfield code="c">12 cm. - 12 cm</subfield><subfield code="e">Beil. (1 S.)</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="b">cd</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="500" ind1=" " ind2=" "><subfield code="a">Rostock, Univ., Diss., 2004</subfield></datafield><datafield tag="650" ind1="0" ind2="7"><subfield code="a">Alkohole</subfield><subfield code="g">sekundär-</subfield><subfield code="0">(DE-588)4343428-9</subfield><subfield code="2">gnd</subfield><subfield code="9">rswk-swf</subfield></datafield><datafield tag="650" ind1="0" ind2="7"><subfield code="a">Lösungsmitteleffekt</subfield><subfield code="0">(DE-588)4168032-7</subfield><subfield code="2">gnd</subfield><subfield code="9">rswk-swf</subfield></datafield><datafield tag="650" ind1="0" ind2="7"><subfield code="a">Katalytische Aktivität</subfield><subfield code="0">(DE-588)4279994-6</subfield><subfield code="2">gnd</subfield><subfield code="9">rswk-swf</subfield></datafield><datafield tag="650" ind1="0" ind2="7"><subfield code="a">Alkoholdehydrogenasen</subfield><subfield code="0">(DE-588)4285029-0</subfield><subfield code="2">gnd</subfield><subfield code="9">rswk-swf</subfield></datafield><datafield tag="650" ind1="0" ind2="7"><subfield code="a">Ketone</subfield><subfield code="0">(DE-588)4129416-6</subfield><subfield code="2">gnd</subfield><subfield code="9">rswk-swf</subfield></datafield><datafield tag="650" ind1="0" ind2="7"><subfield code="a">Reduktion</subfield><subfield code="g">Chemie</subfield><subfield code="0">(DE-588)4277879-7</subfield><subfield code="2">gnd</subfield><subfield code="9">rswk-swf</subfield></datafield><datafield tag="650" ind1="0" ind2="7"><subfield code="a">Lactobacillus brevis</subfield><subfield code="0">(DE-588)4166373-1</subfield><subfield code="2">gnd</subfield><subfield code="9">rswk-swf</subfield></datafield><datafield tag="650" ind1="0" ind2="7"><subfield code="a">Enzymkatalyse</subfield><subfield code="0">(DE-588)4152480-9</subfield><subfield code="2">gnd</subfield><subfield code="9">rswk-swf</subfield></datafield><datafield tag="650" ind1="0" ind2="7"><subfield code="a">Prochiralität</subfield><subfield code="0">(DE-588)4175781-6</subfield><subfield code="2">gnd</subfield><subfield code="9">rswk-swf</subfield></datafield><datafield tag="655" ind1=" " ind2="7"><subfield code="0">(DE-588)4113937-9</subfield><subfield code="a">Hochschulschrift</subfield><subfield code="2">gnd-content</subfield></datafield><datafield tag="689" ind1="0" ind2="0"><subfield code="a">Ketone</subfield><subfield code="0">(DE-588)4129416-6</subfield><subfield code="D">s</subfield></datafield><datafield tag="689" ind1="0" ind2="1"><subfield code="a">Prochiralität</subfield><subfield code="0">(DE-588)4175781-6</subfield><subfield code="D">s</subfield></datafield><datafield tag="689" ind1="0" ind2="2"><subfield code="a">Reduktion</subfield><subfield code="g">Chemie</subfield><subfield code="0">(DE-588)4277879-7</subfield><subfield code="D">s</subfield></datafield><datafield tag="689" ind1="0" ind2="3"><subfield code="a">Enzymkatalyse</subfield><subfield code="0">(DE-588)4152480-9</subfield><subfield code="D">s</subfield></datafield><datafield tag="689" ind1="0" ind2="4"><subfield code="a">Alkoholdehydrogenasen</subfield><subfield code="0">(DE-588)4285029-0</subfield><subfield code="D">s</subfield></datafield><datafield tag="689" ind1="0" ind2="5"><subfield code="a">Alkohole</subfield><subfield code="g">sekundär-</subfield><subfield code="0">(DE-588)4343428-9</subfield><subfield code="D">s</subfield></datafield><datafield tag="689" ind1="0" ind2=" "><subfield code="5">DE-604</subfield></datafield><datafield tag="689" ind1="1" ind2="0"><subfield code="a">Alkoholdehydrogenasen</subfield><subfield code="0">(DE-588)4285029-0</subfield><subfield code="D">s</subfield></datafield><datafield tag="689" ind1="1" ind2="1"><subfield code="a">Lactobacillus brevis</subfield><subfield code="0">(DE-588)4166373-1</subfield><subfield code="D">s</subfield></datafield><datafield tag="689" ind1="1" ind2="2"><subfield code="a">Reduktion</subfield><subfield code="g">Chemie</subfield><subfield code="0">(DE-588)4277879-7</subfield><subfield code="D">s</subfield></datafield><datafield tag="689" ind1="1" ind2="3"><subfield code="a">Katalytische Aktivität</subfield><subfield code="0">(DE-588)4279994-6</subfield><subfield code="D">s</subfield></datafield><datafield tag="689" ind1="1" ind2="4"><subfield code="a">Lösungsmitteleffekt</subfield><subfield code="0">(DE-588)4168032-7</subfield><subfield code="D">s</subfield></datafield><datafield tag="689" ind1="1" ind2=" "><subfield code="5">DE-604</subfield></datafield><datafield tag="856" ind1="4" ind2="2"><subfield code="m">DNB Datenaustausch</subfield><subfield code="q">application/pdf</subfield><subfield code="u">http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=013212223&sequence=000001&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA</subfield><subfield code="3">Inhaltsverzeichnis</subfield></datafield><datafield tag="943" ind1="1" ind2=" "><subfield code="a">oai:aleph.bib-bvb.de:BVB01-013212223</subfield></datafield></record></collection> |
| genre | (DE-588)4113937-9 Hochschulschrift gnd-content |
| genre_facet | Hochschulschrift |
| id | DE-604.BV019888173 |
| illustrated | Not Illustrated |
| indexdate | 2024-08-23T00:13:47Z |
| institution | BVB |
| language | English |
| oai_aleph_id | oai:aleph.bib-bvb.de:BVB01-013212223 |
| oclc_num | 634913196 |
| open_access_boolean | |
| owner | DE-355 DE-BY-UBR |
| owner_facet | DE-355 DE-BY-UBR |
| physical | 1 CD-ROM 12 cm. - 12 cm Beil. (1 S.) |
| publishDate | 2004 |
| publishDateSearch | 2004 |
| publishDateSort | 2004 |
| record_format | marc |
| spelling | Eckstein, Marrit Friederike 1976- Verfasser (DE-588)129958921 aut Alcohol dehydrogenase catalysed reductions in non-conventional media vorgelegt von Marrit Friederike Eckstein 1 CD-ROM ; 12 cm 2004 1 CD-ROM 12 cm. - 12 cm Beil. (1 S.) txt rdacontent c rdamedia cd rdacarrier Rostock, Univ., Diss., 2004 Alkohole sekundär- (DE-588)4343428-9 gnd rswk-swf Lösungsmitteleffekt (DE-588)4168032-7 gnd rswk-swf Katalytische Aktivität (DE-588)4279994-6 gnd rswk-swf Alkoholdehydrogenasen (DE-588)4285029-0 gnd rswk-swf Ketone (DE-588)4129416-6 gnd rswk-swf Reduktion Chemie (DE-588)4277879-7 gnd rswk-swf Lactobacillus brevis (DE-588)4166373-1 gnd rswk-swf Enzymkatalyse (DE-588)4152480-9 gnd rswk-swf Prochiralität (DE-588)4175781-6 gnd rswk-swf (DE-588)4113937-9 Hochschulschrift gnd-content Ketone (DE-588)4129416-6 s Prochiralität (DE-588)4175781-6 s Reduktion Chemie (DE-588)4277879-7 s Enzymkatalyse (DE-588)4152480-9 s Alkoholdehydrogenasen (DE-588)4285029-0 s Alkohole sekundär- (DE-588)4343428-9 s DE-604 Lactobacillus brevis (DE-588)4166373-1 s Katalytische Aktivität (DE-588)4279994-6 s Lösungsmitteleffekt (DE-588)4168032-7 s DNB Datenaustausch application/pdf http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=013212223&sequence=000001&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA Inhaltsverzeichnis |
| spellingShingle | Eckstein, Marrit Friederike 1976- Alcohol dehydrogenase catalysed reductions in non-conventional media Alkohole sekundär- (DE-588)4343428-9 gnd Lösungsmitteleffekt (DE-588)4168032-7 gnd Katalytische Aktivität (DE-588)4279994-6 gnd Alkoholdehydrogenasen (DE-588)4285029-0 gnd Ketone (DE-588)4129416-6 gnd Reduktion Chemie (DE-588)4277879-7 gnd Lactobacillus brevis (DE-588)4166373-1 gnd Enzymkatalyse (DE-588)4152480-9 gnd Prochiralität (DE-588)4175781-6 gnd |
| subject_GND | (DE-588)4343428-9 (DE-588)4168032-7 (DE-588)4279994-6 (DE-588)4285029-0 (DE-588)4129416-6 (DE-588)4277879-7 (DE-588)4166373-1 (DE-588)4152480-9 (DE-588)4175781-6 (DE-588)4113937-9 |
| title | Alcohol dehydrogenase catalysed reductions in non-conventional media |
| title_auth | Alcohol dehydrogenase catalysed reductions in non-conventional media |
| title_exact_search | Alcohol dehydrogenase catalysed reductions in non-conventional media |
| title_full | Alcohol dehydrogenase catalysed reductions in non-conventional media vorgelegt von Marrit Friederike Eckstein |
| title_fullStr | Alcohol dehydrogenase catalysed reductions in non-conventional media vorgelegt von Marrit Friederike Eckstein |
| title_full_unstemmed | Alcohol dehydrogenase catalysed reductions in non-conventional media vorgelegt von Marrit Friederike Eckstein |
| title_short | Alcohol dehydrogenase catalysed reductions in non-conventional media |
| title_sort | alcohol dehydrogenase catalysed reductions in non conventional media |
| topic | Alkohole sekundär- (DE-588)4343428-9 gnd Lösungsmitteleffekt (DE-588)4168032-7 gnd Katalytische Aktivität (DE-588)4279994-6 gnd Alkoholdehydrogenasen (DE-588)4285029-0 gnd Ketone (DE-588)4129416-6 gnd Reduktion Chemie (DE-588)4277879-7 gnd Lactobacillus brevis (DE-588)4166373-1 gnd Enzymkatalyse (DE-588)4152480-9 gnd Prochiralität (DE-588)4175781-6 gnd |
| topic_facet | Alkohole sekundär- Lösungsmitteleffekt Katalytische Aktivität Alkoholdehydrogenasen Ketone Reduktion Chemie Lactobacillus brevis Enzymkatalyse Prochiralität Hochschulschrift |
| url | http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=013212223&sequence=000001&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA |
| work_keys_str_mv | AT ecksteinmarritfriederike alcoholdehydrogenasecatalysedreductionsinnonconventionalmedia |