Synthesis and Properties of Planar-Chiral (η6-Benzene)(η5-cyclopentadienyl)ruthenium(II) Complexes in an Optically Pure Form

Planar-chiral cyclopentadienylruthenium complexes [Ru(η5-1-CO2R*-2-Me-4-R1C5H2)(η6-C6H6)][X] (4 and 8) (R* = (l)- or (d)-menthyl; R1 = Me, Ph, t-Bu, 2-Naphthyl, or 4-BrC6H4; X = PF6 or BPh4) were synthesized in a diastereomerically pure form. The absolute configuration of 8b and 4c (R1 = Ph, t-Bu) w...

Full description

Saved in:
Bibliographic Details
Published inBulletin of the Chemical Society of Japan Vol. 74; no. 3; pp. 527 - 537
Main Authors Matsushima, Yuji, Komatsuzaki, Nobuko, Ajioka, Yoshiki, Yamamoto, Mari, Kikuchi, Hidetomo, Takata, Yasuyuki, Dodo, Noriko, Onitsuka, Kiyotaka, Uno, Mitsunari, Takahashi, Shigetoshi
Format Journal Article
LanguageEnglish
Published Tokyo The Chemical Society of Japan 01.03.2001
Chemical Society of Japan
Online AccessGet full text

Cover

Loading…
Abstract Planar-chiral cyclopentadienylruthenium complexes [Ru(η5-1-CO2R*-2-Me-4-R1C5H2)(η6-C6H6)][X] (4 and 8) (R* = (l)- or (d)-menthyl; R1 = Me, Ph, t-Bu, 2-Naphthyl, or 4-BrC6H4; X = PF6 or BPh4) were synthesized in a diastereomerically pure form. The absolute configuration of 8b and 4c (R1 = Ph, t-Bu) were determined by an X-ray crystallographic analysis and those of the others were assigned on the basis of their optical properties including their CD spectra. Enantiopure complexes (SC1)-[Ru(η5-1-CONHBut-2-Me-4-R1C5H2)(η6-C6H6)][PF6] 9 and -[Ru(η5-1-CONHBut-2-Me-4-R1C5H2)(η6-C6H6)] [BPh4] 10, and (RC1)-9 and -10 were prepared from direct hydrolysis of diastereomeric complexes, followed by the reaction of amines. Replacement reactions of the bromo group in 9e (R1 = 4-BrC6H4) gave alkyl, phenyl, and ethynyl derivatives. Complexes [Ru(η5-1-CO2Et-2-Me-4-R1C5H2)(η6-C6H6)][PF6] 6 were also transformed to planar-chiral [Ru(η5-1-CO2Et-2-Me-4-R1C5H2)(CH3CN)3][X], which underwent ligand exchange reactions to afford carbonyl, phosphine, and π-arene complexes.
AbstractList Abstract Planar-chiral cyclopentadienylruthenium complexes [Ru(η5-1-CO2R*-2-Me-4-R1C5H2)(η6-C6H6)][X] (4 and 8) (R* = (l)- or (d)-menthyl; R1 = Me, Ph, t-Bu, 2-Naphthyl, or 4-BrC6H4; X = PF6 or BPh4) were synthesized in a diastereomerically pure form. The absolute configuration of 8b and 4c (R1 = Ph, t-Bu) were determined by an X-ray crystallographic analysis and those of the others were assigned on the basis of their optical properties including their CD spectra. Enantiopure complexes (SC1)-[Ru(η5-1-CONHBut-2-Me-4-R1C5H2)(η6-C6H6)][PF6] 9 and -[Ru(η5-1-CONHBut-2-Me-4-R1C5H2)(η6-C6H6)] [BPh4] 10, and (RC1)-9 and -10 were prepared from direct hydrolysis of diastereomeric complexes, followed by the reaction of amines. Replacement reactions of the bromo group in 9e (R1 = 4-BrC6H4) gave alkyl, phenyl, and ethynyl derivatives. Complexes [Ru(η5-1-CO2Et-2-Me-4-R1C5H2)(η6-C6H6)][PF6] 6 were also transformed to planar-chiral [Ru(η5-1-CO2Et-2-Me-4-R1C5H2)(CH3CN)3][X], which underwent ligand exchange reactions to afford carbonyl, phosphine, and π-arene complexes.
Planar-chiral cyclopentadienylruthenium complexes [Ru(η5-1-CO2R*-2-Me-4-R1C5H2)(η6-C6H6)][X] (4 and 8) (R* = (l)- or (d)-menthyl; R1 = Me, Ph, t-Bu, 2-Naphthyl, or 4-BrC6H4; X = PF6 or BPh4) were synthesized in a diastereomerically pure form. The absolute configuration of 8b and 4c (R1 = Ph, t-Bu) were determined by an X-ray crystallographic analysis and those of the others were assigned on the basis of their optical properties including their CD spectra. Enantiopure complexes (SC1)-[Ru(η5-1-CONHBut-2-Me-4-R1C5H2)(η6-C6H6)][PF6] 9 and -[Ru(η5-1-CONHBut-2-Me-4-R1C5H2)(η6-C6H6)] [BPh4] 10, and (RC1)-9 and -10 were prepared from direct hydrolysis of diastereomeric complexes, followed by the reaction of amines. Replacement reactions of the bromo group in 9e (R1 = 4-BrC6H4) gave alkyl, phenyl, and ethynyl derivatives. Complexes [Ru(η5-1-CO2Et-2-Me-4-R1C5H2)(η6-C6H6)][PF6] 6 were also transformed to planar-chiral [Ru(η5-1-CO2Et-2-Me-4-R1C5H2)(CH3CN)3][X], which underwent ligand exchange reactions to afford carbonyl, phosphine, and π-arene complexes.
Author Takata, Yasuyuki
Onitsuka, Kiyotaka
Uno, Mitsunari
Matsushima, Yuji
Kikuchi, Hidetomo
Komatsuzaki, Nobuko
Dodo, Noriko
Takahashi, Shigetoshi
Yamamoto, Mari
Ajioka, Yoshiki
Author_xml – sequence: 1
  givenname: Yuji
  surname: Matsushima
  fullname: Matsushima, Yuji
  organization: 1 The Institute of Scientific and Industrial Research, Osaka University8-1 Mihogaoka, Ibaraki, Osaka 567-0047
– sequence: 2
  givenname: Nobuko
  surname: Komatsuzaki
  fullname: Komatsuzaki, Nobuko
  organization: 1 The Institute of Scientific and Industrial Research, Osaka University8-1 Mihogaoka, Ibaraki, Osaka 567-0047
– sequence: 3
  givenname: Yoshiki
  surname: Ajioka
  fullname: Ajioka, Yoshiki
  organization: 1 The Institute of Scientific and Industrial Research, Osaka University8-1 Mihogaoka, Ibaraki, Osaka 567-0047
– sequence: 4
  givenname: Mari
  surname: Yamamoto
  fullname: Yamamoto, Mari
  organization: 1 The Institute of Scientific and Industrial Research, Osaka University8-1 Mihogaoka, Ibaraki, Osaka 567-0047
– sequence: 5
  givenname: Hidetomo
  surname: Kikuchi
  fullname: Kikuchi, Hidetomo
  organization: 1 The Institute of Scientific and Industrial Research, Osaka University8-1 Mihogaoka, Ibaraki, Osaka 567-0047
– sequence: 6
  givenname: Yasuyuki
  surname: Takata
  fullname: Takata, Yasuyuki
  organization: 1 The Institute of Scientific and Industrial Research, Osaka University8-1 Mihogaoka, Ibaraki, Osaka 567-0047
– sequence: 7
  givenname: Noriko
  surname: Dodo
  fullname: Dodo, Noriko
  organization: 1 The Institute of Scientific and Industrial Research, Osaka University8-1 Mihogaoka, Ibaraki, Osaka 567-0047
– sequence: 8
  givenname: Kiyotaka
  surname: Onitsuka
  fullname: Onitsuka, Kiyotaka
  organization: 1 The Institute of Scientific and Industrial Research, Osaka University8-1 Mihogaoka, Ibaraki, Osaka 567-0047
– sequence: 9
  givenname: Mitsunari
  surname: Uno
  fullname: Uno, Mitsunari
  organization: 1 The Institute of Scientific and Industrial Research, Osaka University8-1 Mihogaoka, Ibaraki, Osaka 567-0047
– sequence: 10
  givenname: Shigetoshi
  surname: Takahashi
  fullname: Takahashi, Shigetoshi
  organization: 1 The Institute of Scientific and Industrial Research, Osaka University8-1 Mihogaoka, Ibaraki, Osaka 567-0047
BookMark eNptkM9q3DAQh0VJoZukp76AoJcsxRtL1t9juzTtQiALTc5m7B2zWmzJlWyoe-hr9S36TNWSHHroafjBN98wv0ty4YNHQt6xcsO4ULdNm04bLTaS61dkxSphilJV4oKsyrK0BVe6ekMuUzrlaKSwK_Lr2-KnIyaXKPgD3ccwYpwcJho6uu_BQyy2Rxehpzd_fqviE_qf6HGdgyzape0z7yc4OPRLv45zdnk3Dze73ZpuwzD2-CO7nM92-jBOroW-X-h-jkjvQhyuyesO-oRvX-YVebr7_Lj9Wtw_fNltP94XbSXNVDBdlZ3qJDRcW11aVh2sabRgiBYaVA1KbkBraDqhDXDFhakEVyCFkd0Bqivy_tk7xvB9xjTVpzBHn0_WTEgrFLOWZ-rDM9XGkFLErh6jGyAuNSvrc8H1ueBaizoXnGnzQh9xOD-WQutwWk4wgv_H_5_VvzZPhfQ
CitedBy_id crossref_primary_10_1016_j_apcata_2015_05_039
crossref_primary_10_1007_s11164_020_04263_z
crossref_primary_10_1039_B314859A
crossref_primary_10_1039_C6PY01946C
crossref_primary_10_1021_om0102246
crossref_primary_10_1039_B109666B
crossref_primary_10_1039_C6PY00484A
crossref_primary_10_1039_D3CS00325F
crossref_primary_10_1002_ejic_200300934
crossref_primary_10_1016_j_jorganchem_2005_11_010
crossref_primary_10_1021_ja016334l
crossref_primary_10_1021_acs_macromol_5b02067
crossref_primary_10_1039_c2cc18137a
crossref_primary_10_1002_ange_201300485
crossref_primary_10_1039_D0PY01073A
crossref_primary_10_1016_j_ica_2014_08_057
crossref_primary_10_1039_C5CC02414E
crossref_primary_10_1002_chem_201000011
crossref_primary_10_1021_ja411310w
crossref_primary_10_1002_anie_202113827
crossref_primary_10_1002_ange_202113827
crossref_primary_10_1021_om030688z
crossref_primary_10_1039_b910977c
crossref_primary_10_1002_anie_201300485
crossref_primary_10_1021_ma5008623
crossref_primary_10_1021_ja411869r
crossref_primary_10_1039_b107051g
Cites_doi 10.1016/S0040-4039(98)02603-3
10.1021/om990533k
10.1016/S0040-4039(01)99425-0
10.1021/om9810347
10.1002/anie.199705501
10.1021/cr00080a005
10.1246/bcsj.69.17
10.1021/cr00013a011
10.1021/om00063a014
10.1002/(SICI)1521-3765(19990301)5:3<1055::AID-CHEM1055>3.0.CO;2-K
10.1021/ja981061o
10.1002/anie.199511431
10.1002/cber.19961291102
10.1021/cr00039a007
10.1016/0022-328X(95)05492-8
10.1039/a801291a
10.1021/cr9403695
10.1021/jo951404q
10.1002/(SICI)1521-3765(19991203)5:12<3509::AID-CHEM3509>3.0.CO;2-2
10.1021/om00027a011
10.1016/0022-328X(92)80107-9
10.1021/om990800m
10.1016/S0040-4039(00)91094-3
10.1016/0022-328X(85)80050-4
10.1016/0040-4020(96)00246-3
10.1351/pac198557121749
10.1021/ol991139l
10.1021/om00030a050
10.1002/anie.199612621
ContentType Journal Article
Copyright The Chemical Society of Japan
Copyright Japan Science and Technology Agency 2001
Copyright_xml – notice: The Chemical Society of Japan
– notice: Copyright Japan Science and Technology Agency 2001
DBID AAYXX
CITATION
7SR
8BQ
8FD
JG9
DOI 10.1246/bcsj.74.527
DatabaseName CrossRef
Engineered Materials Abstracts
METADEX
Technology Research Database
Materials Research Database
DatabaseTitle CrossRef
Materials Research Database
Engineered Materials Abstracts
Technology Research Database
METADEX
DatabaseTitleList CrossRef

Materials Research Database
DeliveryMethod fulltext_linktorsrc
Discipline Chemistry
EISSN 1348-0634
EndPage 537
ExternalDocumentID 3130523831
10_1246_bcsj_74_527
FullText_t_NoSnippeting true
GroupedDBID 02
08R
23N
2WC
3O-
41
53G
5GY
ABDEX
ABEFU
ABFLS
ABZEH
ACCUC
ACIWK
ACNCT
ADACO
ADBCX
ADKFC
AENEX
AETEA
AFFNX
AFMIJ
AIDUJ
ALMA_UNASSIGNED_HOLDINGS
CS3
DU5
EBS
EJD
F20
F5P
G8K
GX1
H~9
JSI
JSP
MVM
MYA
OHT
OK1
P0W
P2P
RAD
RJT
RZJ
SC5
TKC
TN5
TWZ
UPT
VH1
VQP
WH7
X
X7J
XPZ
ZCG
ZE2
ZY4
-~X
0R~
6J9
6TJ
AAPXW
AAUAY
AAYXX
ABTAH
ABXVV
ACGFO
ADIPN
AI.
BCRHZ
CITATION
KOP
OJZSN
OWPYF
ROX
~02
7SR
8BQ
8FD
JG9
ID FETCH-LOGICAL-c358t-1730f6f5ab27970913d98b741ee9abe6be528a77abf478a262483426a5485fda3
ISSN 0009-2673
IngestDate Tue Sep 24 21:39:07 EDT 2024
Thu Sep 12 17:51:58 EDT 2024
Tue Jan 05 20:24:28 EST 2021
IsPeerReviewed true
IsScholarly true
Issue 3
Language English
LinkModel OpenURL
MergedId FETCHMERGED-LOGICAL-c358t-1730f6f5ab27970913d98b741ee9abe6be528a77abf478a262483426a5485fda3
PQID 1459461992
PQPubID 1996365
PageCount 11
ParticipantIDs proquest_journals_1459461992
crossref_primary_10_1246_bcsj_74_527
chemicalsocietyjapan_journals_10_1246_bcsj_74_527
ProviderPackageCode RAD
PublicationCentury 2000
PublicationDate 2001-03-00
PublicationDateYYYYMMDD 2001-03-01
PublicationDate_xml – month: 03
  year: 2001
  text: 2001-03-00
PublicationDecade 2000
PublicationPlace Tokyo
PublicationPlace_xml – name: Tokyo
PublicationTitle Bulletin of the Chemical Society of Japan
PublicationTitleAlternate Bulletin of the Chemical Society of Japan
PublicationYear 2001
Publisher The Chemical Society of Japan
Chemical Society of Japan
Publisher_xml – name: The Chemical Society of Japan
– name: Chemical Society of Japan
References c) N. Komatsuzaki, M. Uno, K. Shirai, Y. Takai, T. Tanaka, M. Sawada, and S. Takahashi,Bull. Chem. Soc. Jpn., 69, 17 (1996).
18) a) A. Suzuki,Pure Appl. Chem., 57, 1749 (1985).
17) I. Klement, M. Rottländer, C. E. Tucker, T. N. Majid, and P. Knochel,Tetrahedron, 52, 7201 (1996).
b) D. Enders, R. Peters, J. Runsink, and J. W. Bats,Org. Lett., 1, 1863 (1999).
c) E. Cesarotti, A. Chiesa, G. F. Ciani, and A. Sironi,J. Chem. Soc., Dalton Trans., 1984, 653.
b) E. Sesarotti, M. Angoletta, N. P. C. Walker, M. B. Hursthouse, R. Vefghi, P. A. Schofield, and C. White,J. Organomet. Chem., 286, 343 (1985).
b) Y. Morimoto, K. Ando, M. Uno, and S. Takahashi,Chem. Commun., 1997, 1795.
5) a) H. H. Brintzinger, D. Fischer, R. Mülhaupt, B. Rieger, and R. M. Waymouth,Angew. Chem., Int. Ed. Engl., 34, 1143 (1995).
8) a) Y. Morimoto, K. Ando, M. Uno, and S. Takahashi,Chem. Lett., 1996, 887.
b) R. L. Halterman,Chem. Rev., 92, 965 (1992).
b) N. Miyaura and A. Suzuki,Chem. Rev., 95, 2457 (1995).
14) N. Komatsuzaki, M. Uno, H. Kikuchi, and S. Takahashi,Chem. Lett., 1996, 677.
b) T. Watanabe and M. Uemura,Chem. Commun., 1998, 871.
12) a) T. Naota, H. Takaya, and S. Murahashi,Chem. Rev., 98, 2599 (1998).
b) N. Komatsuzaki, M. Uno, K. Shirai, T. Tanaka, M. Sawada, and S. Takahashi,J. Organomet. Chem., 498, 53 (1995).
19) K. Sonogashira, Y. Tohda, and N. Hagihara,Tetrahedron Lett., 16, 4467 (1975).
c) Y. Ie and G. C. Fu,Chem. Commun., 2000, 119.
3) a) C. Bolm and K. Muñiz,Chem. Soc. Rev., 28, 51 (1999).
16) D. T. Gltzhofer, Y. Liang, and M. A. Khan,Organometallics, 12, 624 (1993).
b) S. E. Kegley, K. A. Walter, D. T. Bergstrom, D. K. MacFarland, B. C. Young, and A. L. Rheingold,Organometallics, 12, 2339 (1993).
1) a) G. Consiglio and F. Morandini,Chem. Rev., 87, 761 (1987).
13) a) A. Mezzetti and G. Consiglio,J. Organomet. Chem., 430, C15 (1992).
c) R. Kuwano, T. Uemura, M. Saitoh, and Y. Ito,Tetrahedron Lett., 40, 1327 (1999).
7) C. E. Garrett and G. C. Fu,J. Am. Chem. Soc., 120, 7479 (1998).
15) M. Hatanaka, Y. Himeda, and I. Ueda,J. Chem. Soc., Perkin Trans. 1, 1993, 2269.
c) J. A. Gladysz and B. J. Boone,Angew. Chem., Int. Ed. Engl., 36, 550 (1997).
b) B. M. Trost,Chem. Ber., 129, 1313 (1996).
6) a) J. B. Thomson,Tetrahedron Lett., 6, 26 (1959).
11) T. P. Gill and K. R. Mann,Organometallics, 1, 485 (1982).
c) Y. Morisaki, T. Kondo, and T. Mitsudo,Organometallics, 18, 4742 (1999).
2) a) B. M. Trost, B. Vidal, and M. Thommen,Chem. Eur. J., 5, 1055 (1999).
c) K. Kamikawa, T. Watanabe, and M. Uemura,J. Org. Chem., 61, 1375 (1996).
9) a) M. Uno, K. Shirai, K. Ando, N. Komatsuzaki, T. Tanaka, M. Sawada, and S. Takahashi,Chem. Lett., 1995, 7.
10) M. Uno, K. Ando, N. Komatsuzaki, and S. Takahashi,J. Chem. Soc., Chem. Commun., 1992, 964.
4) a) H. Nishiyama, T. Naitoh, Y. Motoyama, and K. Aoki,Chem. Eur. J., 5, 3509 (1999).
b) Y. Kataoka, Y. Iwato, T. Yamagata, and K. Tani,Organometallics, 18, 5423 (1999).
b) A. H. Hoveyda and J. P. Morken,Angew. Chem., Int. Ed. Engl., 35, 1262 (1996).
c) T. Katayama, Y. Morimoto, M. Yuge, M. Uno, and S. Takahashi,Organometallics, 18, 3087 (1999).
2024012006084797500_r1
2024012006084797500_r26
2024012006084797500_r27
2024012006084797500_r24
2024012006084797500_r25
2024012006084797500_r22
2024012006084797500_r23
2024012006084797500_r20
2024012006084797500_r21
2024012006084797500_r9
2024012006084797500_r8
2024012006084797500_r7
2024012006084797500_r6
2024012006084797500_r5
2024012006084797500_r4
2024012006084797500_r3
2024012006084797500_r2
2024012006084797500_r19
2024012006084797500_r17
2024012006084797500_r18
2024012006084797500_r15
2024012006084797500_r37
2024012006084797500_r16
2024012006084797500_r38
2024012006084797500_r13
2024012006084797500_r35
2024012006084797500_r14
2024012006084797500_r36
2024012006084797500_r11
2024012006084797500_r33
2024012006084797500_r12
2024012006084797500_r34
2024012006084797500_r31
2024012006084797500_r10
2024012006084797500_r32
2024012006084797500_r30
2024012006084797500_r28
2024012006084797500_r29
References_xml – ident: 2024012006084797500_r6
  doi: 10.1016/S0040-4039(98)02603-3
– ident: 2024012006084797500_r28
  doi: 10.1021/om990533k
– ident: 2024012006084797500_r21
– ident: 2024012006084797500_r14
  doi: 10.1016/S0040-4039(01)99425-0
– ident: 2024012006084797500_r20
  doi: 10.1021/om9810347
– ident: 2024012006084797500_r3
  doi: 10.1002/anie.199705501
– ident: 2024012006084797500_r1
  doi: 10.1021/cr00080a005
– ident: 2024012006084797500_r8
– ident: 2024012006084797500_r23
  doi: 10.1246/bcsj.69.17
– ident: 2024012006084797500_r2
  doi: 10.1021/cr00013a011
– ident: 2024012006084797500_r25
  doi: 10.1021/om00063a014
– ident: 2024012006084797500_r4
  doi: 10.1002/(SICI)1521-3765(19990301)5:3<1055::AID-CHEM1055>3.0.CO;2-K
– ident: 2024012006084797500_r17
  doi: 10.1021/ja981061o
– ident: 2024012006084797500_r32
– ident: 2024012006084797500_r12
  doi: 10.1002/anie.199511431
– ident: 2024012006084797500_r19
– ident: 2024012006084797500_r27
  doi: 10.1002/cber.19961291102
– ident: 2024012006084797500_r24
– ident: 2024012006084797500_r37
  doi: 10.1021/cr00039a007
– ident: 2024012006084797500_r22
  doi: 10.1016/0022-328X(95)05492-8
– ident: 2024012006084797500_r7
  doi: 10.1039/a801291a
– ident: 2024012006084797500_r26
  doi: 10.1021/cr9403695
– ident: 2024012006084797500_r9
  doi: 10.1021/jo951404q
– ident: 2024012006084797500_r10
  doi: 10.1002/(SICI)1521-3765(19991203)5:12<3509::AID-CHEM3509>3.0.CO;2-2
– ident: 2024012006084797500_r34
  doi: 10.1021/om00027a011
– ident: 2024012006084797500_r29
  doi: 10.1016/0022-328X(92)80107-9
– ident: 2024012006084797500_r5
  doi: 10.1021/om990800m
– ident: 2024012006084797500_r38
  doi: 10.1016/S0040-4039(00)91094-3
– ident: 2024012006084797500_r30
  doi: 10.1016/0022-328X(85)80050-4
– ident: 2024012006084797500_r35
  doi: 10.1016/0040-4020(96)00246-3
– ident: 2024012006084797500_r36
  doi: 10.1351/pac198557121749
– ident: 2024012006084797500_r15
  doi: 10.1021/ol991139l
– ident: 2024012006084797500_r18
– ident: 2024012006084797500_r16
– ident: 2024012006084797500_r11
  doi: 10.1021/om00030a050
– ident: 2024012006084797500_r31
– ident: 2024012006084797500_r33
– ident: 2024012006084797500_r13
  doi: 10.1002/anie.199612621
SSID ssj0008549
Score 1.7660803
Snippet Planar-chiral cyclopentadienylruthenium complexes [Ru(η5-1-CO2R*-2-Me-4-R1C5H2)(η6-C6H6)][X] (4 and 8) (R* = (l)- or (d)-menthyl; R1 = Me, Ph, t-Bu,...
Abstract Planar-chiral cyclopentadienylruthenium complexes [Ru(η5-1-CO2R*-2-Me-4-R1C5H2)(η6-C6H6)][X] (4 and 8) (R* = (l)- or (d)-menthyl; R1 = Me, Ph, t-Bu,...
SourceID proquest
crossref
chemicalsocietyjapan
SourceType Aggregation Database
Publisher
StartPage 527
Title Synthesis and Properties of Planar-Chiral (η6-Benzene)(η5-cyclopentadienyl)ruthenium(II) Complexes in an Optically Pure Form
URI http://dx.doi.org/10.1246/bcsj.74.527
https://www.proquest.com/docview/1459461992/abstract/
Volume 74
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3dbtMwFLbKuAAuEDDQBgP5YpNWTSltaufnklUb66QNJDZpu4rsxNHSn6RqU4n2gtfiLXgH3oRz4sRttArBbqLWsZ3E54t9jnPOdwjZjxwViQ4yXEZKWiz0mCVdl1vKDz3b9du-G6OheHHpnF2z8xt-02j8XvNamueyFS43xpU8RKpQBnLFKNn_kKzpFArgN8gXjiBhOP6TjL8tUtDfkFKk9PmfoJe0ppHFbERiavXuEgzBBz3yoHdycOw61rFKl6pgFzWF3AoX4QgTaeWFB9hiBGen6PueJpgH2ev3cfcA546R-l64cMEVj75Mio3w0eLoK36GOAX1t_aNuGT2rtwQDDdB5SkK5eewVht4Xoh8Np_dJeNCob2dDxKzHGRjPLcUOsn2ZSbnw8xgdZBkQ90kg9ZD0-pWjAUgMStjkpLaDseai1eripH7-x1Wc7tv2Y5OjNJSejrvMs8CJYytz_c6K1CJ6-7a5M01S0GpB3BNRnNvibELbmUZzgYtl7VMmxpnN1pWUC_AWoHLAqj1iDwG7HPcH_h8s_JC8nhloembL0NIofHHtUs8I9thOQIzPQADfPi6LlVXJQr96OoFeV4aNvSTRulL0lDpK_KkV-UT3CY_DFopoJWu0EqzmNbQSg9__TQ4bcKf-_hsGnQe9vtNapBJkxR6pwaZFJFJEZmvyfXpyVXvzCqzf1hhl3u51YG1J3ZiLiSMm4v0tZHvSVCAlfKFVI5U3PaE6woZM9cTtmPjvrjtCLDBeRyJ7huylWap2iEUbRiv7UdR6LcZs9uiE0q_K6ESD31uq13S2TS8Qfmqz4IN8twl-9XYBxNNDLO52l4ll7XuGPeZg47fbx9w5Xfk6eot2SNb-XSu3oNmnMsPBbb-ABNtwCc
link.rule.ids 315,786,790,27957,27958
linkProvider Geneva Foundation for Medical Education and Research
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Synthesis+and+Properties+of+Planar-Chiral+%28%CE%B76-Benzene%29%28%CE%B75-cyclopentadienyl%29ruthenium%28II%29+Complexes+in+an+Optically+Pure+Form&rft.jtitle=Bulletin+of+the+Chemical+Society+of+Japan&rft.au=Matsushima%2C+Yuji&rft.au=Komatsuzaki%2C+Nobuko&rft.au=Ajioka%2C+Yoshiki&rft.au=Yamamoto%2C+Mari&rft.date=2001-03-01&rft.pub=The+Chemical+Society+of+Japan&rft.issn=0009-2673&rft.eissn=1348-0634&rft.volume=74&rft.issue=3&rft.spage=527&rft.epage=537&rft_id=info:doi/10.1246%2Fbcsj.74.527&rft.externalDocID=10_1246_bcsj_74_527
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0009-2673&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0009-2673&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0009-2673&client=summon