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Explored Reactions containing Reaction Structure in CASREACT.
Input structure:
OHOHOHOHOHProductOH
13 Reactions
Copyrights:
CAPLUS: Copyright 2009 American Chemical Society. All Rights Reserved. (The UK patent
material in this product/service is UK Crown copyright and is made available with
permission. Crown Copyright. The French (FR) patent material in this product/service is made available from Institut National de la Propriete Industrielle (INPI).)
MEDLINE: Produced by the U.S. National Library of Medicine
REGISTRY: Copyright 2009 American Chemical Society. All Rights Reserved. (Some records
contain information from GenBank(R). See also: Benson D.A., Karsch-Mizrachi I., Lipman D.J., Ostell J., Rapp B.A., Wheeler D.L. Genbank. Nucl. Acids Res. 28(1):15-18 (2000). Property values tagged with IC are from the ZIC/VINITI data file provided by InfoChem.) CAS Registry is a service mark of the American Chemical Society.
CASREACT: Copyright 2009 American Chemical Society. All Rights Reserved. CASREACT
contains reactions from CAS and from: ZIC/VINITI database (1974-1999) provided by InfoChem; INPI data prior to 1986; Biotransformations database compiled under the
direction of Professor Dr. Klaus Kieslich; organic reactions, portions copyright 1996-2006 John Wiley & Sons, Ltd., John Wiley and Sons, Inc., Organic Reactions Inc., and Organic Syntheses Inc. Reproduced under license. All Rights Reserved.
CHEMLIST, CHEMCATS: Copyright 2009 American Chemical Society. All Rights Reserved.
MeHCHO+HOCMe1.1 R:NaOH, S:H2O, S:Xylene, 2.5 h, rt reflux; 4.5 h, reflux; reflux rt2.1 R:BBr3, S:CH2Cl2, rt 3.5C; 3.5C; 15 h, rtOMe2.2 R:H2O, 40 min, rtOHOHOHOHMeMeCMeHOCMeMeHOCMeMeCMeOHHOOHMeCMeMeCOHMeMeCOHMeMeCOHMeOHOHOHOH
Faming Zhuanli Shenqing Gongkai Shuomingshu, 101367713, 18 Feb 2009 CASREACT
(Copyright (C) 2011 ACS. In addition to reactions indexed by CAS, CASREACT contains reactions derived from the following sources: ZIC/VINITI database (1974-1999) provided by
InfoChem, INPI data prior to 1986, and Biotransformations database compiled under the direction of Professor Dr. Klaus Kieslich.)
NOTE: 1) paraformaldehyde used, 2) optimization study, Reactants: 2, Reagents: 3, Solvents: 3, Steps: 2, Stages: 3, Most stages in any one step: 2OMeOMeOMeOMeMeCMeMeCMeOHMeCMeOHMeCMeOHHOOHMeCMeMeCOHMeMeCOHMeMeCOHMeOMeOMeOMeOMe1.1 R:BBr3, S:CH2Cl2, rt 3.5C; 3.5C; 15 h, rt1.2 R:H2O, 40 min, rt
OHOHOHOHMeMeCMeHOCMeMeHOCMeMeCMeOHHOOHMeCMeMeCOHMeMeCOHMeMeCOHMeOHOH92%OHOHNOTE: optimization study, Reactants: 1, Reagents: 2, Solvents: 1, Steps: 1, Stages: 2
Faming Zhuanli Shenqing Gongkai Shuomingshu, 101367713, 18 Feb 2009 CASREACT
(Copyright (C) 2011 ACS. In addition to reactions indexed by CAS, CASREACT contains reactions derived from the following sources: ZIC/VINITI database (1974-1999) provided by
InfoChem, INPI data prior to 1986, and Biotransformations database compiled under the direction of Professor Dr. Klaus Kieslich.)
HOt-BuSiMe2Cl+MeCMeOH+HCHO(Step 2.1)1.1 R:1H-Imidazole, S:DMF1.2 S:H2O2.1 R:KOH, S:H2O, S:Xylene3.1 R:Bu4N+ F-, 3.2 R:HCl, S:H2OS:MeOH, S:THFOHOHOHOHMeMeCMeHOCMeMeHOCMeMeCMeOHHOOHMeCMeMeCOHMeMeCOHMeMeCOHMeOHOHOHOHNOTE: 2) paraformaldehyde used, Reactants: 3, Reagents: 4, Solvents: 5, Steps: 3, Stages: 5, Most stages in any one step: 2
Bulletin of the Korean Chemical Society, 21(8), 813-816; 2000 CASREACT
(Copyright (C) 2011 ACS. In addition to reactions indexed by CAS, CASREACT contains reactions derived from the following sources: ZIC/VINITI database (1974-1999) provided by
InfoChem, INPI data prior to 1986, and Biotransformations database compiled under the direction of Professor Dr. Klaus Kieslich.)
HOt-BuSiMe2Cl+MeCMeOH+HCHO(Step 2.1)1.1 R:1H-Imidazole, S:DMF1.2 S:H2O2.1 R:KOH, S:H2O, S:Xylene3.1 R:Bu4N+ F-, 3.2 R:HCl, S:H2OS:MeOH, S:THFOHOHOHMeCMeMeCMeMeCMeOHOHHOHOOHMeCMeOHOHRHOMeCMeOHMeCMeOHRMeCMeOHNOTE: 2) paraformaldehyde used, Reactants: 3, Reagents: 4, Solvents: 5, Steps: 3, Stages: 5, Most stages in any one step: 2
Bulletin of the Korean Chemical Society, 21(8), 813-816; 2000 CASREACT
(Copyright (C) 2011 ACS. In addition to reactions indexed by CAS, CASREACT contains reactions derived from the following sources: ZIC/VINITI database (1974-1999) provided by
InfoChem, INPI data prior to 1986, and Biotransformations database compiled under the direction of Professor Dr. Klaus Kieslich.)
HOt-BuSiMe2Cl+MeCMeOH+HCHO(Step 2.1)1.1 R:1H-Imidazole, S:DMF1.2 S:H2O2.1 R:KOH, S:H2O, S:Xylene3.1 R:Bu4N+ F-, 3.2 R:HCl, S:H2OS:MeOH, S:THFOHOHMeCMeMeCMeHOMeHOCHOMeOHHOOHOHMeCMeOHMeCMeMeCMeOHOH
Bulletin of the Korean Chemical Society, 21(8), 813-816; 2000 CASREACT
(Copyright (C) 2011 ACS. In addition to reactions indexed by CAS, CASREACT contains reactions derived from the following sources: ZIC/VINITI database (1974-1999) provided by
InfoChem, INPI data prior to 1986, and Biotransformations database compiled under the direction of Professor Dr. Klaus Kieslich.)
NOTE: 2) paraformaldehyde used, Reactants: 3, Reagents: 4, Solvents: 5, Steps: 3, Stages: 5, Most stages in any one step: 2MeCHCHO+HOMeOSiMeBu-t1.1 R:KOH, S:H2O, S:Xylene2.1 R:Bu4N+ F-, S:MeOH, S:THF2.2 R:HCl, S:H2OMeOHOHOHOHMeMeCMeHOCMeMeHOCMeMeCMeOHHOOHMeCMeMeCOHMeMeCOHMeMeCOHMeOHOHOHOH
Bulletin of the Korean Chemical Society, 21(8), 813-816; 2000 CASREACT
(Copyright (C) 2011 ACS. In addition to reactions indexed by CAS, CASREACT contains reactions derived from the following sources: ZIC/VINITI database (1974-1999) provided by
InfoChem, INPI data prior to 1986, and Biotransformations database compiled under the direction of Professor Dr. Klaus Kieslich.)
NOTE: 1) paraformaldehyde used, Reactants: 2, Reagents: 3, Solvents: 4, Steps: 2, Stages: 3, Most stages in any one step: 2MeCHCHO+HOMeOSiMeBu-t1.1 R:KOH, S:H2O, S:Xylene2.1 R:Bu4N+ F-, S:MeOH, S:THF2.2 R:HCl, S:H2OMeOHOHOHMeCMeMeCMeMeCMeOHOHHOHOOHMeCMeOHOHRHOMeCMeOHMeCMeOHRMeCMeOHNOTE: 1) paraformaldehyde used, Reactants: 2, Reagents: 3, Solvents: 4, Steps: 2, Stages: 3, Most stages in any one step: 2
Bulletin of the Korean Chemical Society, 21(8), 813-816; 2000 CASREACT
(Copyright (C) 2011 ACS. In addition to reactions indexed by CAS, CASREACT contains reactions derived from the following sources: ZIC/VINITI database (1974-1999) provided by
InfoChem, INPI data prior to 1986, and Biotransformations database compiled under the direction of Professor Dr. Klaus Kieslich.)
MeCHCHO+HOMeOSiMeBu-t1.1 R:KOH, S:H2O, S:Xylene2.1 R:Bu4N+ F-, S:MeOH, S:THF2.2 R:HCl, S:H2OMeOHOHMeCMeMeCMeHOMeHOCHOMeOHHOOHOHMeCMeOHMeCMeMeCMeOHOH
Bulletin of the Korean Chemical Society, 21(8), 813-816; 2000 CASREACT
(Copyright (C) 2011 ACS. In addition to reactions indexed by CAS, CASREACT contains reactions derived from the following sources: ZIC/VINITI database (1974-1999) provided by
InfoChem, INPI data prior to 1986, and Biotransformations database compiled under the direction of Professor Dr. Klaus Kieslich.)
NOTE: 1) paraformaldehyde used, Reactants: 2, Reagents: 3, Solvents: 4, Steps: 2, Stages: 3, Most stages in any one step: 2OHOHOHOHMeMeCMeHOCMeMeHOCMeMeCMeMULTIPAGEIMAGE307529-71-11.1 R:Bu4N+ F-, 1.2 R:HCl, S:H2OS:MeOH, S:THFOHHOOHMeCMeMeCOHMeMeCOHMeMeCOHMeOHOH84%OHOH
Bulletin of the Korean Chemical Society, 21(8), 813-816; 2000 CASREACT
(Copyright (C) 2011 ACS. In addition to reactions indexed by CAS, CASREACT contains reactions derived from the following sources: ZIC/VINITI database (1974-1999) provided by
InfoChem, INPI data prior to 1986, and Biotransformations database compiled under the direction of Professor Dr. Klaus Kieslich.)
Met-BuSiMeOt-BuMeSiMeOt-BuMeSiMeONOTE: Reactants: 1, Reagents: 2, Solvents: 3, Steps: 1, Stages: 2MeCMeMeCMeMeCMeMet-BuSiMeOMeCMeOHOHOHOHHOMeCMeOMeSiMeBu-tMeMeCOHMeOHMeCMeMet-BuSiMeOOSiMeBu-t1.1 R:Bu4N+ F-, 1.2 R:HCl, S:H2OS:MeOH, S:THF
OHOHOHMeCMeMeCMeMeCMeOHOHHOHOOHMeCMeOHOHRHOMeCMeOHMeCMeOHRMeCMeOH92%
Bulletin of the Korean Chemical Society, 21(8), 813-816; 2000 CASREACT
(Copyright (C) 2011 ACS. In addition to reactions indexed by CAS, CASREACT contains reactions derived from the following sources: ZIC/VINITI database (1974-1999) provided by
InfoChem, INPI data prior to 1986, and Biotransformations database compiled under the direction of Professor Dr. Klaus Kieslich.)
NOTE: Reactants: 1, Reagents: 2, Solvents: 3, Steps: 1, Stages: 2Met-BuSiMeOOMeSiMeBu-tMeCMeMeCMeMet-BuSiMeOMeHOCHOMeOHHOOHMeOHCMeOMeSiMeBu-tMeCMeMeCMeMet-BuSiMeOOMeSiMeBu-t1.1 R:Bu4N+ F-, S:MeOH, S:THF1.2 R:HCl, S:H2O
OHOHMeCMeMeCMeHOMeHOCHOMeOHHOOHOHMeCMeOHMeCMeMeCMeOH91%OHNOTE: Reactants: 1, Reagents: 2, Solvents: 3, Steps: 1, Stages: 2
Bulletin of the Korean Chemical Society, 21(8), 813-816; 2000 CASREACT
(Copyright (C) 2011 ACS. In addition to reactions indexed by CAS, CASREACT contains reactions derived from the following sources: ZIC/VINITI database (1974-1999) provided by
InfoChem, INPI data prior to 1986, and Biotransformations database compiled under the direction of Professor Dr. Klaus Kieslich.)
MeHCHO+HOCMe1.1 R:KOH, S:PhMe, S:H2O2.1 R:BBr3, S:CH2Cl22.2 R:H2OOMeOHOHOHOHMeMeCMeHOCMeMeHOCMeMeCMeOHHOOHMeCMeMeCOHMeMeCOHMeMeCOHMeOHOHOHOHNOTE: 1) no other calixarene was detected, Reactants: 2, Reagents: 3, Solvents: 3, Steps: 2, Stages: 3, Most stages in any one step: 2
Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry, (2), 185-188; 1997 CASREACT
(Copyright (C) 2011 ACS. In addition to reactions indexed by CAS, CASREACT contains reactions derived from the following sources: ZIC/VINITI database (1974-1999) provided by
InfoChem, INPI data prior to 1986, and Biotransformations database compiled under the direction of Professor Dr. Klaus Kieslich.)
OMeOMeOMeOMeMeMeCMeCMeOHMeCMeOHMeCMe1.1 R:BBr3, S:CH2Cl2OHHO1.2 R:H2OOHMeCMeMeCOHMeMeCOHMeMeCOHMeOMeOMeOMeOMeOHOHOHOHMeCMeMeHOCMeMeHOCMeMeCMeOHHOOHMeCMeMeCOHMeMeCOHMeMeCOHMeOHOH79%OHOH
NOTE: Reactants: 1, Reagents: 2, Solvents: 1, Steps: 1, Stages: 2
Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry, (2), 185-188; 1997 CASREACT
(Copyright (C) 2011 ACS. In addition to reactions indexed by CAS, CASREACT contains reactions derived from the following sources: ZIC/VINITI database (1974-1999) provided by
InfoChem, INPI data prior to 1986, and Biotransformations database compiled under the direction
of Professor Dr. Klaus Kieslich.)
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