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Extract from the Register of European Patents

EP About this file: EP1820790

EP1820790 - 3-alkylated-5,5',6,6',7,7',8,8'-octahydro-2,2'-binaphthols and 3,3'-dialkylated-5,5',6,6',7,7',8,8'-octahydro-2,2'-binaphthols and processes for making them [Right-click to bookmark this link]
Former [2007/34]3-Alkylated-5,5',6,6',7,7',8,8'-octahydro-2,2'binaphthols and 3,3'-dialkylated-5,5',6,6',7,7',8,8'-octahydro-2,2'-binaphthols and process for making them
[2009/49]
StatusNo opposition filed within time limit
Status updated on  16.03.2012
Database last updated on 11.09.2024
Most recent event   Tooltip27.09.2013Lapse of the patent in a contracting state
New state(s): TR
published on 30.10.2013  [2013/44]
Applicant(s)For all designated states
INVISTA Technologies S.à.r.l.
Talstrasse 80
8001 Zürich / CH
[2007/49]
Former [2007/34]For all designated states
E.I. du Pont de Nemours and Company
1007 Market Street
Wilmington, DE 19898 / US
Inventor(s)01 / Lu, Helen S.M.
209 Knoll Road
Wallingford, PA 19086 / US
02 / Qiu, Weiming
303 Charleston Drive
Wilmington DE 19808 / US
03 / Shapiro, Rafael
1415 Fresno Road
Wilmington DE 19803 / US
 [2010/50]
Former [2007/34]01 / Lu, Helen S.M.
209 Knoll Road
Wallingford, PA 19086 / US
02 / Qiu, Weiming
303 Charleton Drive
Wilmington DE 19808 / US
03 / Shapiro, Rafael
1415 Fresno Road
Wilmington DE 19803 / US
Representative(s)Cockerton, Bruce Roger, et al
Carpmaels & Ransford LLP
One Southampton Row
London WC1B 5HA / GB
[N/P]
Former [2009/30]Cockerton, Bruce Roger, et al
Carpmaels & Ransford 43-45 Bloomsbury Square London
WC1A 2RA / GB
Former [2007/34]Cockerton, Bruce Roger, et al
Carpmaels & Ransford, 43 Bloomsbury Square
London WC1A 2RA / GB
Application number, filing date07010025.020.11.2002
[2007/34]
Priority number, dateUS2001099409926.11.2001         Original published format: US 994099
[2007/34]
Filing languageEN
Procedural languageEN
PublicationType: A2 Application without search report 
No.:EP1820790
Date:22.08.2007
Language:EN
[2007/34]
Type: A3 Search report 
No.:EP1820790
Date:25.11.2009
[2009/48]
Type: B1 Patent specification 
No.:EP1820790
Date:11.05.2011
Language:EN
[2011/19]
Search report(s)(Supplementary) European search report - dispatched on:EP26.10.2009
ClassificationIPC:C07C39/17, C07C37/14, C07C37/18, C07C37/11, C07C37/16
[2009/48]
CPC:
C07C39/17 (EP,KR,US); C07C37/11 (EP,US); C07C37/14 (EP,US);
C07C37/16 (EP,US); C07C37/18 (EP,US); C07C2601/10 (EP,US);
C07C2602/10 (EP,US) (-)
C-Set:
C07C37/11, C07C39/17 (US,EP);
C07C37/14, C07C39/17 (EP,US);
C07C37/16, C07C39/17 (US,EP);
C07C37/18, C07C39/17 (US,EP)
Former IPC [2007/34]C07C39/17
Designated contracting statesAT,   BE,   BG,   CH,   CY,   CZ,   DE,   DK,   EE,   ES,   FI,   FR,   GB,   GR,   IE,   IT,   LI,   LU,   MC,   NL,   PT,   SE,   SK,   TR [2007/34]
TitleGerman:3-alkylierte 5,5',6,6',7,7',8,8'-octahydro-2,2'Binaphthole und 3,3'-dialkylierte 5,5',6,6',7,7',8,8'-octahydro-2,2'-Binaphthole sowie Herstellungsverfahren dafür[2007/34]
English:3-alkylated-5,5',6,6',7,7',8,8'-octahydro-2,2'-binaphthols and 3,3'-dialkylated-5,5',6,6',7,7',8,8'-octahydro-2,2'-binaphthols and processes for making them[2009/49]
French:Binaphtholes 2,2 d'alkylat 3-octoahydro-3-5,5',6,6',7,7', et binaphtholes 2,2- d'alkylat 3,3-octoahydro-3-5,5',6,6',7,7'8,8' et leur processus de fabrication[2009/49]
Former [2007/34]3-Alkylated-5,5',6,6',7,7',8,8'-octahydro-2,2'binaphthols and 3,3'-dialkylated-5,5',6,6',7,7',8,8'-octahydro-2,2'-binaphthols and process for making them
Former [2007/34]Binaphtholes2,2 d'alkylat 3-octoahydro-3-5,5',6,6',7,7', et binaphtholes2,2- d'alkylat 3,3-octoahydro-3-5,5',6,6',7,7'8,8' et leur processus de fabrication
Examination procedure19.04.2010Amendment by applicant (claims and/or description)
29.04.2010Examination requested  [2010/23]
18.11.2010Communication of intention to grant the patent
17.03.2011Fee for grant paid
17.03.2011Fee for publishing/printing paid
Parent application(s)   TooltipEP02789788.3  / EP1465851
Divisional application(s)EP10179048.3  / EP2275397
EP10179062.4  / EP2279994
Opposition(s)14.02.2012No opposition filed within time limit [2012/16]
Fees paidRenewal fee
21.05.2007Renewal fee patent year 03
21.05.2007Renewal fee patent year 04
21.05.2007Renewal fee patent year 05
21.05.2007Renewal fee patent year 06
31.03.2008Renewal fee patent year 07
12.11.2009Renewal fee patent year 08
12.11.2010Renewal fee patent year 09
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Responsibility for the accuracy, completeness or quality of the data displayed under the link provided lies entirely with the Unified Patent Court.
Lapses during opposition  TooltipAT11.05.2011
CY11.05.2011
CZ11.05.2011
DK11.05.2011
EE11.05.2011
FI11.05.2011
SE11.05.2011
SK11.05.2011
TR11.05.2011
BG11.08.2011
GR12.08.2011
PT12.09.2011
IE20.11.2011
LU20.11.2011
CH30.11.2011
LI30.11.2011
MC30.11.2011
[2013/44]
Former [2013/29]AT11.05.2011
CY11.05.2011
CZ11.05.2011
DK11.05.2011
EE11.05.2011
FI11.05.2011
SE11.05.2011
SK11.05.2011
BG11.08.2011
GR12.08.2011
PT12.09.2011
IE20.11.2011
LU20.11.2011
CH30.11.2011
LI30.11.2011
MC30.11.2011
Former [2013/25]AT11.05.2011
CY11.05.2011
CZ11.05.2011
DK11.05.2011
EE11.05.2011
FI11.05.2011
SE11.05.2011
SK11.05.2011
GR12.08.2011
PT12.09.2011
IE20.11.2011
LU20.11.2011
CH30.11.2011
LI30.11.2011
MC30.11.2011
Former [2012/47]AT11.05.2011
CY11.05.2011
CZ11.05.2011
DK11.05.2011
EE11.05.2011
FI11.05.2011
SE11.05.2011
SK11.05.2011
GR12.08.2011
PT12.09.2011
IE20.11.2011
CH30.11.2011
LI30.11.2011
MC30.11.2011
Former [2012/33]AT11.05.2011
CY11.05.2011
CZ11.05.2011
DK11.05.2011
EE11.05.2011
FI11.05.2011
SE11.05.2011
SK11.05.2011
GR12.08.2011
PT12.09.2011
CH30.11.2011
LI30.11.2011
MC30.11.2011
Former [2012/29]AT11.05.2011
CY11.05.2011
CZ11.05.2011
DK11.05.2011
EE11.05.2011
FI11.05.2011
SE11.05.2011
SK11.05.2011
GR12.08.2011
PT12.09.2011
MC30.11.2011
Former [2012/11]AT11.05.2011
CY11.05.2011
CZ11.05.2011
DK11.05.2011
EE11.05.2011
FI11.05.2011
SE11.05.2011
SK11.05.2011
GR12.08.2011
PT12.09.2011
Former [2012/09]AT11.05.2011
CY11.05.2011
CZ11.05.2011
EE11.05.2011
FI11.05.2011
SE11.05.2011
GR12.08.2011
PT12.09.2011
Former [2012/01]AT11.05.2011
CY11.05.2011
FI11.05.2011
SE11.05.2011
GR12.08.2011
PT12.09.2011
Former [2011/49]CY11.05.2011
FI11.05.2011
SE11.05.2011
GR12.08.2011
PT12.09.2011
Former [2011/47]PT12.09.2011
Documents cited:Search[PA]  - R. R. SCHROCK ET AL, "New Chiral Molybdenum Catalysts for Asymmetric Olefin Metathesis that Contain 3,3'-Disubstituted Octahydrobinaphtholate or 2,6-Dichlorophenylimido Ligands", ORGANOMETALLICS., ACS, COLUMBUS, OH., US, (20020121), vol. 21, no. 2, ISSN 0276-7333, pages 409 - 417, XP002232516 [PA] 1-3 * page 410, column R *

DOI:   http://dx.doi.org/10.1021/om0107441
 [A]  - S. L. AEILTS ET AL, "A Readily Available and User-Friendly Chiral Catalyst for Efficient Enantioselective Olefin Metathesis", ANGEWANDTE CHEMIE. INTERNATIONAL EDITION, VERLAG CHEMIE. WEINHEIM, DE, (20010417), vol. 40, no. 8, ISSN 0570-0833, pages 1452 - 1456, XP001004954 [A] 1-6 * page 1455, column R *

DOI:   http://dx.doi.org/10.1002/1521-3773(20010417)40:8<1452::AID-ANIE1452>3.0.CO;2-G
by applicantUS5235113
 WO9906146
 WO9962855
    - AEILTS, S. L. ET AL., Angewandte Chemie International Edition, VERLAG CHEMIE, (20010417), vol. 40, pages 1452 - 1456
    - TETRAHEDRON LETT., (1997), page 5273
The EPO accepts no responsibility for the accuracy of data originating from other authorities; in particular, it does not guarantee that it is complete, up to date or fit for specific purposes.