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1
(1- 13C)Alditols: elimination of magnetic equivalence in 1H-and 13C-n.m.r. spectra of symmetric compounds through ( 13C)-substitution
(1- 13C)Alditols: elimination of magnetic equivalence in 1H-and 13C-n.m.r. spectra of symmetric compounds through ( 13C)-substitution
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(1- 13C)Alditols: elimination of magnetic equivalence in 1H-and 13C-n.m.r. spectra of symmetric compounds through ( 13C)-substitution

Carbohydrate research, 1990-12, Vol.208, p.23-35 [Peer Reviewed Journal]

1990 ;1993 INIST-CNRS ;ISSN: 0008-6215 ;EISSN: 1873-426X ;DOI: 10.1016/0008-6215(90)80082-E ;PMID: 1964871 ;CODEN: CRBRAT

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2
1:1 and 2:1 Charge-Transfer Complexes between Aromatic Hydrocarbons and Dry Titanium Dioxide
1:1 and 2:1 Charge-Transfer Complexes between Aromatic Hydrocarbons and Dry Titanium Dioxide
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1:1 and 2:1 Charge-Transfer Complexes between Aromatic Hydrocarbons and Dry Titanium Dioxide

Angewandte Chemie (International ed.), 2005-01, Vol.44 (6), p.910-913 [Peer Reviewed Journal]

Copyright © 2005 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;ISSN: 1433-7851 ;EISSN: 1521-3773 ;DOI: 10.1002/anie.200461972 ;PMID: 15624219

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3
1,1'-Carbonylbis(3-methylimidazolium) triflate: an efficient reagent for aminoacylations
1,1'-Carbonylbis(3-methylimidazolium) triflate: an efficient reagent for aminoacylations
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1,1'-Carbonylbis(3-methylimidazolium) triflate: an efficient reagent for aminoacylations

Journal of the American Chemical Society, 1989-06, Vol.111 (13), p.4856-4859 [Peer Reviewed Journal]

1990 INIST-CNRS ;ISSN: 0002-7863 ;EISSN: 1520-5126 ;DOI: 10.1021/ja00195a043 ;CODEN: JACSAT

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4
1,1'-Thiocarbonyldi-2,2'-pyridone. A new useful reagent for functional group conversions under essentially neutral conditions
1,1'-Thiocarbonyldi-2,2'-pyridone. A new useful reagent for functional group conversions under essentially neutral conditions
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1,1'-Thiocarbonyldi-2,2'-pyridone. A new useful reagent for functional group conversions under essentially neutral conditions

Journal of organic chemistry, 1986-06, Vol.51 (13), p.2613-2615 [Peer Reviewed Journal]

1986 INIST-CNRS ;ISSN: 0022-3263 ;EISSN: 1520-6904 ;DOI: 10.1021/jo00363a046 ;CODEN: JOCEAH

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5
1:10-Phenanthroline and mono-, di-, tri- and tetra-methyl-1:10-phenanthrolines as chelated copper complex cations
1:10-Phenanthroline and mono-, di-, tri- and tetra-methyl-1:10-phenanthrolines as chelated copper complex cations
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1:10-Phenanthroline and mono-, di-, tri- and tetra-methyl-1:10-phenanthrolines as chelated copper complex cations

Analyst (London), 1952, Vol.77 (921), p.846 [Peer Reviewed Journal]

ISSN: 0003-2654 ;EISSN: 1364-5528 ;DOI: 10.1039/an9527700846

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6
1,1,1,3,3,3-Hexafluoropropan-2-ol as a solvent for the generation of highly persistent radical cations
1,1,1,3,3,3-Hexafluoropropan-2-ol as a solvent for the generation of highly persistent radical cations
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1,1,1,3,3,3-Hexafluoropropan-2-ol as a solvent for the generation of highly persistent radical cations

Journal of the Chemical Society, Perkin Transactions 2, 1995 (9), p.1735 [Peer Reviewed Journal]

ISSN: 0300-9580 ;EISSN: 1364-5471 ;DOI: 10.1039/p29950001735

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7
1,1,2,2-Tetrafluoroethyl- N, N-dimethylamine: a new selective fluorinating agent
1,1,2,2-Tetrafluoroethyl- N, N-dimethylamine: a new selective fluorinating agent
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1,1,2,2-Tetrafluoroethyl- N, N-dimethylamine: a new selective fluorinating agent

Journal of Fluorine Chemistry, 2001-06, Vol.109 (1), p.25-31 [Peer Reviewed Journal]

2001 Elsevier Science B.V. ;ISSN: 0022-1139 ;EISSN: 1873-3328 ;DOI: 10.1016/S0022-1139(01)00372-4

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8
1,1′-Biadamantane-3,3′-diol: a two-dimensional network supported by a `hexameric alcohol cluster' supramolecular synthon
1,1′-Biadamantane-3,3′-diol: a two-dimensional network supported by a `hexameric alcohol cluster' supramolecular synthon
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1,1′-Biadamantane-3,3′-diol: a two-dimensional network supported by a `hexameric alcohol cluster' supramolecular synthon

Acta crystallographica. Section C, Crystal structure communications, 2013-02, Vol.69 (2), p.175-178 [Peer Reviewed Journal]

International Union of Crystallography, 2013 ;ISSN: 0108-2701 ;EISSN: 1600-5759 ;DOI: 10.1107/S0108270112051785 ;PMID: 23377686

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9
1,1′‐Binaphthyldiamine‐Based Lewis Bases as Readily Available and Efficient Organocatalysts for the Reduction of N‐Aryl and N‐Alkyl Ketimines
1,1′‐Binaphthyldiamine‐Based Lewis Bases as Readily Available and Efficient Organocatalysts for the Reduction of N‐Aryl and N‐Alkyl Ketimines
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1,1′‐Binaphthyldiamine‐Based Lewis Bases as Readily Available and Efficient Organocatalysts for the Reduction of N‐Aryl and N‐Alkyl Ketimines

European Journal of Organic Chemistry, 2009-08, Vol.2009 (22), p.3683-3687 [Peer Reviewed Journal]

Copyright © 2009 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;2009 INIST-CNRS ;ISSN: 1434-193X ;EISSN: 1099-0690 ;DOI: 10.1002/ejoc.200900524

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10
1,1′-Bis(2-pyridylthio)ferrocene: a new ligand in gold and silver chemistry
1,1′-Bis(2-pyridylthio)ferrocene: a new ligand in gold and silver chemistry
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1,1′-Bis(2-pyridylthio)ferrocene: a new ligand in gold and silver chemistry

Dalton : an international journal of inorganic chemistry, 2001 (17), p.2523-2529

ISSN: 1472-7773 ;EISSN: 1364-5447 ;DOI: 10.1039/b102636b

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11
1,1′-Bi(trishomobarrelenyl) - Synthesis and Chiroptic Properties
1,1′-Bi(trishomobarrelenyl) - Synthesis and Chiroptic Properties
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1,1′-Bi(trishomobarrelenyl) - Synthesis and Chiroptic Properties

European Journal of Organic Chemistry, 2009-03, Vol.2009 (7), p.1048-1052 [Peer Reviewed Journal]

Copyright © 2009 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;2009 INIST-CNRS ;ISSN: 1434-193X ;EISSN: 1099-0690 ;DOI: 10.1002/ejoc.200801111

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12
1,1′-OXALYLDIIMIDAZOLE, A NEW REAGENT FOR ACTIVATION OF CARBOXYLIC ACID
1,1′-OXALYLDIIMIDAZOLE, A NEW REAGENT FOR ACTIVATION OF CARBOXYLIC ACID
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1,1′-OXALYLDIIMIDAZOLE, A NEW REAGENT FOR ACTIVATION OF CARBOXYLIC ACID

Chemistry letters, , Vol.12 (12), p.1819-1820 [Peer Reviewed Journal]

The Chemical Society of Japan ;1984 INIST-CNRS ;ISSN: 0366-7022 ;EISSN: 1348-0715 ;DOI: 10.1246/cl.1983.1819 ;CODEN: CMLTAG

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13
1,2-Addition of Alkyl- and Alkenylzirconocene Chlorides to Aldehydes Accelerated by Catalytic Amounts of ZnBr2 as a Method of Synthesizing Secondary Alcohols, Secondary Allylic Alcohols, and in-Situ Oppenauer-Type Oxidation of the Alcohols to Ketones
1,2-Addition of Alkyl- and Alkenylzirconocene Chlorides to Aldehydes Accelerated by Catalytic Amounts of ZnBr2 as a Method of Synthesizing Secondary Alcohols, Secondary Allylic Alcohols, and in-Situ Oppenauer-Type Oxidation of the Alcohols to Ketones
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1,2-Addition of Alkyl- and Alkenylzirconocene Chlorides to Aldehydes Accelerated by Catalytic Amounts of ZnBr2 as a Method of Synthesizing Secondary Alcohols, Secondary Allylic Alcohols, and in-Situ Oppenauer-Type Oxidation of the Alcohols to Ketones

Journal of organic chemistry, 1995-06, Vol.60 (11), p.3278-3279 [Peer Reviewed Journal]

ISSN: 0022-3263 ;EISSN: 1520-6904 ;DOI: 10.1021/jo00116a007

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14
1,2-Addition Reaction of Monosubstituted Disilenes:  An Ab Initio Study
1,2-Addition Reaction of Monosubstituted Disilenes:  An Ab Initio Study
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1,2-Addition Reaction of Monosubstituted Disilenes:  An Ab Initio Study

Organometallics, 2004-11, Vol.23 (24), p.5768-5778 [Peer Reviewed Journal]

Copyright © 2004 American Chemical Society ;ISSN: 0276-7333 ;EISSN: 1520-6041 ;DOI: 10.1021/om049418m

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15
1,2-bis(diphenylphosphino)ethane tetrahalide: A convenient reagent for the conversion of alcohols to the corresponding halides
1,2-bis(diphenylphosphino)ethane tetrahalide: A convenient reagent for the conversion of alcohols to the corresponding halides
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1,2-bis(diphenylphosphino)ethane tetrahalide: A convenient reagent for the conversion of alcohols to the corresponding halides

Tetrahedron letters, 1987, Vol.28 (7), p.767-768 [Peer Reviewed Journal]

1987 ;1987 INIST-CNRS ;ISSN: 0040-4039 ;EISSN: 1873-3581 ;DOI: 10.1016/S0040-4039(01)80984-9 ;CODEN: TELEAY

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16
1,2-CARBONYL TRANSPOSITION IN SOME KETONES
1,2-CARBONYL TRANSPOSITION IN SOME KETONES
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1,2-CARBONYL TRANSPOSITION IN SOME KETONES

Chemistry letters, 1976-12, Vol.5 (12), p.1319-1322 [Peer Reviewed Journal]

The Chemical Society of Japan ;ISSN: 0366-7022 ;EISSN: 1348-0715 ;DOI: 10.1246/cl.1976.1319

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17
1,2-CARBONYL TRANSPOSITION OF CIS-BICYCLO[3.3.O]OCTAN-2-ONE TO ITS 3-ONE SKELETON: APPLICATION TO SYNTHESES OF dl-HIRSUTIC ACID AND dl-9(0)-METHANOPROSTACYCLIN
1,2-CARBONYL TRANSPOSITION OF CIS-BICYCLO[3.3.O]OCTAN-2-ONE TO ITS 3-ONE SKELETON: APPLICATION TO SYNTHESES OF dl-HIRSUTIC ACID AND dl-9(0)-METHANOPROSTACYCLIN
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1,2-CARBONYL TRANSPOSITION OF CIS-BICYCLO[3.3.O]OCTAN-2-ONE TO ITS 3-ONE SKELETON: APPLICATION TO SYNTHESES OF dl-HIRSUTIC ACID AND dl-9(0)-METHANOPROSTACYCLIN

Chemistry letters, 1981-09, Vol.10 (9), p.1245-1248 [Peer Reviewed Journal]

The Chemical Society of Japan ;ISSN: 0366-7022 ;EISSN: 1348-0715 ;DOI: 10.1246/cl.1981.1245

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18
1,2-cis-C-glycoside synthesis by samarium diiodide-promoted radical cyclizations
1,2-cis-C-glycoside synthesis by samarium diiodide-promoted radical cyclizations
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1,2-cis-C-glycoside synthesis by samarium diiodide-promoted radical cyclizations

Chemistry : a European journal, 1997-08, Vol.3 (8), p.1342-1356 [Peer Reviewed Journal]

Copyright © 1997 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;ISSN: 0947-6539 ;EISSN: 1521-3765 ;DOI: 10.1002/chem.19970030822

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19
1,2-Diacyl-Phosphatidylcholine Flip-Flop Measured Directly by Sum-Frequency Vibrational Spectroscopy
1,2-Diacyl-Phosphatidylcholine Flip-Flop Measured Directly by Sum-Frequency Vibrational Spectroscopy
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1,2-Diacyl-Phosphatidylcholine Flip-Flop Measured Directly by Sum-Frequency Vibrational Spectroscopy

Biophysical journal, 2005-10, Vol.89 (4), p.2522-2532 [Peer Reviewed Journal]

2005 The Biophysical Society ;Copyright Biophysical Society Oct 2005 ;Copyright © 2005, Biophysical Society 2005 ;ISSN: 0006-3495 ;EISSN: 1542-0086 ;DOI: 10.1529/biophysj.105.065672 ;PMID: 16085770

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20
1,2‐Diarylethanols by Alternative Regioselective Reductive Ring‐Opening of 2,3‐Diaryloxiranes
1,2‐Diarylethanols by Alternative Regioselective Reductive Ring‐Opening of 2,3‐Diaryloxiranes
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1,2‐Diarylethanols by Alternative Regioselective Reductive Ring‐Opening of 2,3‐Diaryloxiranes

European Journal of Organic Chemistry, 2009-02, Vol.2009 (6), p.938-944 [Peer Reviewed Journal]

Copyright © 2009 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;ISSN: 1434-193X ;EISSN: 1099-0690 ;DOI: 10.1002/ejoc.200800992

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