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Steric and Stereoelectronic Effects in Organic Chemistry

Steric and Stereoelectronic Effects in Organic Chemistry (Hardcover, 2, 2021)

Veejendra K. Yadav (지은이)
  |  
Springer
2021-07-02
  |  
319,480원

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Steric and Stereoelectronic Effects in Organic Chemistry

책 정보

· 제목 : Steric and Stereoelectronic Effects in Organic Chemistry (Hardcover, 2, 2021) 
· 분류 : 외국도서 > 과학/수학/생태 > 과학 > 화학 > 유기화학
· ISBN : 9783030756215
· 쪽수 : 262쪽

목차

Chapter-I: Steric and stereoelectronic control of molecular structures and organic reactions

1.       Influence of steric effects on structures

2.       Influence of stereoelectronic effects on reactions

3.       Evaluation of the numerical value of anomeric effect

4.       Influence of anomeric effect on conformational preferences

5.       Influence of anomeric effect on conformational Reactivities

6.       Conformations of mono and dithioacetals

7.       Conformations of mono and diazaacetals

8.       Antiperiplanar effects arising from C-Si, C-Ge and C-Sn bonds
Chapter-II. Reactions at saturated and unsaturated carbons

1.       Inter and intramolecular reactions at saturated carbons

2.       Intermolecular reactions of epoxides

3.       Intramolecular reactions of epoxides

4.       Baldwin’s rules for ring closure at saturated and unsaturated Carbons

5.       SN2’ reaction (reaction at unsaturated carbon)

6.       SN2 reactions of cyclopropanes activated by two geminal carbonyl groups

7.       Reactions involving consecutive intramolecular SN2 reactions leading to rearrangement

8.       Dual activation for skeletal rearrangement

9.       Solvolysis with neighbouring group participation

10.   Rearrangement originating from oxiranes under Lewis acid conditions

11.   Rearrangement via classical vs non-classical carbocations

12.   Tandem skeletal changes and polyene cyclization

13.   Application of Baldwin’s 5-exo-trig cyclization

14.   Stereocontrol in multi-cyclisation

15.   Reaction at sp carbon

16.   Beckman rearrangement


17. Curtius rearrangement

Chapter-III: Diastereoselectivity in organic reactions

1.       Cram’s model for asymmetric synthesis

2.       Anh-Felkin modification of Cram’s model for asymmetric synthesis

3.       Cieplak’s model for diastereoselectivity

4.       Houk’s transition state and electrostatic models for diastereoselectivity

5.       Cation coordination model for diastereoselectivity

Chapter-IV: A(1,2) and A(1,3) strains

1.       Introduction

2.       A(1,2) strain

3.       Stereocontrol in reactions on account of A(1,2) strain

4.       A(1,3) strain

5.       Stereocontrol in reactions on account of A(1,3) strain

6.       A(1,3) strain in amides and its consequences on diastereoselectivity

Chapter-V: The conservation of orbital symmetry (Woodward-Hoffmann rules)

1.       Introduction

2.       Orbitals and symmetry considerations

0.    ?2 + ?2 reaction

3.       Electrocyclic ring closure and ring opening reactions

1.    ?4 + ?2 reaction (Diels-Alder cycloaddition reaction)

Chapter-VI: The overlap component of the stereoelectronic factor vis-a-vis the conservation of orbital symmetry rules

1.       Introduction

2.       Steric effects in the thermal fragmentation of cis-3,6-dimethyl-3,6-dihydropyridazine

3.       Orbital overlap effects in the thermal fragmentation of cyclopropanated and cyclobutanated cis-3,6-dimethyl-3,6-dihydropyridazine

4.       Orbital overlap effects in [1,5]-sigmatropic shifts

5.       Difficulties experienced with the [1,5]-sigmatropic shift in cyclobutanated species

Chapter VII: Torquoselectivity of conrotatory ring opening in 3-substituted cyclobutenes

1. Activation Barrier Approach to Torquoselectivity


2.       TS-NBO Approach to Torquoselectivity

3.       Conformational effects on Torquoselectivity

Chapter-VIII: Hammett Substituent Constants

1.   Hammett substituent constants for benzoic acids (?m and ?p)

2.   Hammett substituent constants for phenylacetic and 3-arylpropionic acids

3. Hammett substituent constants and free energy relationship

4. Hammett substituent constants and reaction pathway assessment

5. Hammett substituent constants ?+ and ?-

6. Hammett substituent constants and ester hydrolysis mechanism

Chapter-IX. Relative aromaticity of pyrrole, furan, thiophene and selenophene, and their Diels-Alder stereoselectivity

1.       Introduction

2.       Heteroatom lone pair interaction with the ring p bonds in the ground state

3.       DA reactions of pyrrole, furan, thiophene and selenophene with maleic anhydride

4.       4.1. DA reactions of cyclopentadiene, silole and germole with maleic anhydride

4.2 DA reactions of cyclopentadiene, silole and germole with acetylene-1,2-bisnitrile and

acetylene

5.1. DA reactions of 1,3-cyclohexadiene and 1,3-cycloheptadiene with maleic anhydride

5.2. DA reactions of 1,3-cyclohexadiene and 1,3-cycloheptadiene with acetylene-1,2-bisnitrile and

acetylene

6.   DA reactions of 1,3-cyclohexadiene and 1,3-cyclooctadiene-6-yne with acetylene-1,2-bisnitrile
and acetylene

7.   Evaluation of the allylic interaction in the DA reactions of acyclic dienes

8. DA reactions of 6-oxa-, 6-aza-, 6-thia- and 6-selena-1,3-cycloheptadiene with maleic anhydride

9. DA reactions of 2,3-cyclopropano-, 2,3-cyclobutano- and 2,3-cyclopentano-6-oxa-1,3-cycloheptadienes with maleic anhydride

10. DA reactions of benzene, pyridine and 1,4-diazine with acetylene-1,2-bisnitrile and acetylene

11. DA reactions of naphthalene, 1-azanaphthalene and 1,4-diazanaphthalene with cyclopropene

12. DA reactions of anthracene, 9-azaanthracene and 9,10-diazaanthracene with cyclopropene

13. DA reactions of benzene, naphthalene, and anthracene with acetylene-1,2-bisnitrile

14. Deformation energy considerations in the DA reactions of five-membered heterocycles with acetylene-1,2-bisnitrile

15. DA reactions of thiophene 1,1-dioxide with maleic anhydride


16. Reaction profile and solvent effects on the diastereoselectivity of DA reactions of five-membered heterocycles with maleic anhydride

Chapter-X: Miscellaneous

1.       Spiroconjugation

2.       Periselectivity

3.       Ambident nucleophiles

4.       Ambident electrophiles

0.    ?-Effect

5.       Carbenes

6.       Hammond postulate

7.       Curtin-Hammett principle

8.       Diastereotopic, homotopic, and enantiotopic substituents

9.       Captodative effect


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