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The Resource Designed molecular space in material science and catalysis, Seiji Shirakawa, editor

Designed molecular space in material science and catalysis, Seiji Shirakawa, editor

Label
Designed molecular space in material science and catalysis
Title
Designed molecular space in material science and catalysis
Statement of responsibility
Seiji Shirakawa, editor
Contributor
Editor
Subject
Language
eng
Member of
Cataloging source
N$T
Dewey number
541.395
Illustrations
illustrations
Index
no index present
LC call number
QD505
Literary form
non fiction
Nature of contents
  • dictionaries
  • bibliography
http://library.link/vocab/relatedWorkOrContributorName
Shirakawa, Seiji
http://library.link/vocab/subjectName
  • Materials science
  • Catalysis
  • Chemistry, Physical and theoretical
Label
Designed molecular space in material science and catalysis, Seiji Shirakawa, editor
Instantiates
Publication
Antecedent source
unknown
Bibliography note
Includes bibliographical references
Carrier category
online resource
Carrier category code
cr
Carrier MARC source
rdacarrier
Color
multicolored
Content category
text
Content type code
txt
Content type MARC source
rdacontent
Contents
  • Chapter 3: Inherently Chiral Calix[4]arenes as Supramolecular Catalysts3.1 Introduction; 3.2 Inherently Chiral Calix[4]arenes with ABCC Substitution Pattern; 3.2.1 Aminophenol-Type Inherently Chiral Calix[4]arenes; 3.2.2 Inherently Chiral Calix[4]arene Amino Acid and its Derivatives; 3.3 Inherently Chiral Calix[4]arenes with ABCD Substitution Pattern; 3.4 Conclusions; References; Chapter 4: Synthesis of the Longest Carbohelicene by Multiple Oxidative Photocyclizations of Arylene-Vinylene Oligomers; 4.1 Introduction; 4.2 History of Longer Carbohelicenes
  • 4.3 Helicene Synthesis by Oxidative Photocyclization4.4 Synthetic Guideline for Precursor Stilbenes Toward Longer Helicenes; 4.5 [9]Helicene; 4.6 [16]Helicene; 4.6.1 TIPSO-[2]+[1]+[1]+[2]+[1]+[1]+[2]-OTIPS Precursor; 4.6.2 Sextuple Photocyclization; 4.6.3 X-Ray Crystal Structure; 4.6.4 Conversion to Unsubstituted [16]Helicene; 4.7 Conclusion; References; Chapter 5: Design of the Chiral Environment for Asymmetric Acid-Base Catalysis; 5.1 Introduction; 5.2 Conformationally Flexible Guanidine/Bisthiourea Organocatalysts; 5.2.1 Enantiodivergent Mannich-Type Reactions
Dimensions
unknown
Extent
1 online resource
File format
unknown
Form of item
online
Isbn
9789811312564
Level of compression
unknown
Media category
computer
Media MARC source
rdamedia
Media type code
c
Other physical details
illustrations (some color)
Quality assurance targets
not applicable
Reformatting quality
unknown
Sound
unknown sound
Specific material designation
remote
Label
Designed molecular space in material science and catalysis, Seiji Shirakawa, editor
Publication
Antecedent source
unknown
Bibliography note
Includes bibliographical references
Carrier category
online resource
Carrier category code
cr
Carrier MARC source
rdacarrier
Color
multicolored
Content category
text
Content type code
txt
Content type MARC source
rdacontent
Contents
  • Chapter 3: Inherently Chiral Calix[4]arenes as Supramolecular Catalysts3.1 Introduction; 3.2 Inherently Chiral Calix[4]arenes with ABCC Substitution Pattern; 3.2.1 Aminophenol-Type Inherently Chiral Calix[4]arenes; 3.2.2 Inherently Chiral Calix[4]arene Amino Acid and its Derivatives; 3.3 Inherently Chiral Calix[4]arenes with ABCD Substitution Pattern; 3.4 Conclusions; References; Chapter 4: Synthesis of the Longest Carbohelicene by Multiple Oxidative Photocyclizations of Arylene-Vinylene Oligomers; 4.1 Introduction; 4.2 History of Longer Carbohelicenes
  • 4.3 Helicene Synthesis by Oxidative Photocyclization4.4 Synthetic Guideline for Precursor Stilbenes Toward Longer Helicenes; 4.5 [9]Helicene; 4.6 [16]Helicene; 4.6.1 TIPSO-[2]+[1]+[1]+[2]+[1]+[1]+[2]-OTIPS Precursor; 4.6.2 Sextuple Photocyclization; 4.6.3 X-Ray Crystal Structure; 4.6.4 Conversion to Unsubstituted [16]Helicene; 4.7 Conclusion; References; Chapter 5: Design of the Chiral Environment for Asymmetric Acid-Base Catalysis; 5.1 Introduction; 5.2 Conformationally Flexible Guanidine/Bisthiourea Organocatalysts; 5.2.1 Enantiodivergent Mannich-Type Reactions
Dimensions
unknown
Extent
1 online resource
File format
unknown
Form of item
online
Isbn
9789811312564
Level of compression
unknown
Media category
computer
Media MARC source
rdamedia
Media type code
c
Other physical details
illustrations (some color)
Quality assurance targets
not applicable
Reformatting quality
unknown
Sound
unknown sound
Specific material designation
remote

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