Stereoelectronic Effects: A Bridge Between Structure and Reactivity

Acknowledgement ix

Supplementory Material x

1 Introduction 1

1.1 Stereoelectronic effects – orbital interactions in control of structure and reactivity 1

1.2 Orbital interactions in theoretical chemistry 3

1.3 The birth of stereoelectronic concepts in organic chemistry 4

References 6

2 Direct Effects of Orbital Overlap on Reactivity 8

2.1 Bond formation without bond breaking: types of overlap in two -orbital interactions 9

2.1.1 Factors controlling σ -bond overlap 12

2.2 Bond formation coupled with bond breaking 25

2.2.1 Three -orbital interactions: stereoelectronic reasons for the preferred trajectories of intermolecular attack at a chemical bond 25

2.3 Stereoelectronics of supramolecular interactions 29

2.3.1 FMO interactions in intermolecular complexes 29

2.3.2 Expanding the palette of supramolecular interactions: from H -bonding to Li -, halogen, pnictogen, chalcogen and tetrel binding 30

References 36

3 Beyond Orbital Overlap: Additional Factors Important for Orbital Interactions. Classifying Delocalizing Interactions 42

3.1 Electronic count: two ]electron, one ]electron and three ]electron bonds 43

3.2 Isovalent vs. sacrificial conjugation 48

3.3 Neutral, negative, and positive hyperconjugation 49

References 52

4 Computational and Theoretical Approaches for Studies of Stereoelectronic Effects 54

4.1 Quantifying orbital interactions 54

4.2 Localized orbitals from delocalized wavefunctions 56

References 60

5 General Stereoelectronic Trends – Donors, Acceptors, and Chameleons 62

5.1 Three types of delocalization: conjugation, hyperconjugation, and σ -conjugation 62

5.2 Geminal and vicinal interactions 63

5.3 Stereoelectronic main rule: antiperiplanarity 64

5.3.1 Effects of bond polarity 65

5.3.2 Polarity -induced acceptor anisotropy 68

5.4 Scales of donor and acceptor ability of orbitals: polarization, hybridization, and orbital energy effects 68

5.4.1 Donors 68

5.4.2 Acceptors 81

5.4.3 Stereoelectronic chameleons: donors masquerading as acceptors 84

5.5 Cooperativity of stereoelectronic effects and antiperiplanar lone pair hypothesis (ALPH) theory – several donors working together 91

5.6 Summary 92

References 92

6 Stereoelectronic Effects with Donor and Acceptor Separated by a Single Bond Bridge: The Broad Spectrum  of Orbital Contributions to Conformational Analysis 97

6.1 σ/σ -Interactions 99

6.1.1 Rotational barrier in ethane 99

6.1.2 Axial/equatorial equilibrium in methylcyclohexane 105

6.1.3 The gauche effect 110

6.2 σ/π -Interactions 113

6.2.1 “Eclipsed” and “staggered” conformations of alkenes – stereoelectronic misnomers 114

6.2.2 Carbonyls 117

6.2.3 Strained bonds 121

6.3 p/σ -Interactions 122

6.3.1 Primary, secondary, tertiary carbocation stabilization 122

6.3.2 Hyperconjomers of cyclohexyl cations 124

6.3.3 β -Silicon effect and related β -effects 124

6.4 n/σ -Interactions 126

6.4.1 Anomeric effects 129

6.4.2 Reverse anomeric effect 142

6.4.3 “Anomeric effects without lone pairs”: beyond the n→σ* interactions 143

6.5 n/π -Interactions 147

6.5.1 Esters and related carboxylic acid derivatives 147

6.5.2 Vinyl ethers and enamines 157

6.6 π/π -Interactions 167

6.6.1 Hyperconjugation in alkynes and its relation to the “absence” of conjugation between two triple bonds in 1,3 -diynes 168

References 170

7 Stereoelectronic Effects with Donor and Acceptor Separated by a Vinyl Bridge 183

7.1 σ/σ* interactions 184

7.1.1 Cis -effect: the case of two σ -acceptors 184

7.2 σ/π interactions: allenes vs. alkenes 185

7.2.1 Neutral systems 185

7.2.2 Anions 186

7.2.3 Positive conjugation and hyperconjugation in vinyl systems 187

7.2.4 σ→π* delocalization in allenes: allenyl silanes in reactions with electrophiles 188

7.3 Vinyl halides and their carbanions (transition from σC -H→σ*C ]Hal to nC→σ*C -Hal interactions) 192

7.3.1 Heteroatom -containing systems 195

7.4 Diazenes and the isomerization of azo compounds 196

7.5 Antiperiplanarity in coordinated bond -breaking and bond -forming processes: eliminations, fragmentations and additions 199

7.6 Syn -periplanarity: the second best choice 207

References 208

8 Remote Stereoelectronic Effects 214

8.1 Extended through space interactions: homoconjugation and homohyperconjugation 215

8.1.1 Homoconjugation 215

8.1.2 Homoanomeric effects 217

8.1.3 Cross -hyperconjugation 223

8.2 Double hyperconjugation and through -bond interactions 223

8.3 Combined through -bond and through -space interactions 228

8.4 Symmetry and cooperativity effects in cyclic structures 229

8.4.1 Hyperaromaticity 229

8.4.2 σ -Aromaticity 230

8.4.3 Double aromaticity 231

References 231

9 Transition State Stabilization with Stereoelectronic Effects: Stereoelectronic Control of Reaction Bottlenecks 236

9.1 Torquoselectivity 240

9.2 Diastereoselection in nucleophilic addition to carbonyl compounds and other π -systems 243

9.3 Electrophilic addition to enamines 245

9.4 Hyperconjugative assistance to alkyne bending and alkyne cycloadditions 246

9.5 Negative conjugation – donation from oxygen lone pairs to breaking bonds 248

9.6 Remote lone pairs in radical reactions: fragmentations 251

References 254

10 Stereoelectronic Effects in Reaction Design 257

10.1 Static stereoelectronics 257

10.2 Dynamic stereoelectronics 259

References 273

11 Stereoelectronic Effects in Action: The Many Doors Opened by Orbital Interactions 275

11.1 Gauche effect (σ→σ* interactions) 275

11.2 Trans -effect – the cousin of gauche effect in organometallic chemistry 283

11.3 Anomeric effects (n→σ* interactions) 284

11.3.1 Cooperativity and anticooperativity in anomeric systems 288

11.3.2 Spectrum of armed and disarmed glycosides 289

11.3.3 Restoring exo -anomeric effect in carbasugars 294

11.4 Bioorganic chemistry and enzyme reactions 311

References 316

12 Probing Stereoelectronic Effects with Spectroscopic Methods 322

12.1 Infrared spectroscopy 323

12.1.1 Bohlmann effect 323

12.1.2 Red -shifting hydrogen bonds – an intermolecular version of the Bohlmann effect 331

12.2 Nuclear magnetic resonance spectroscopy 335

12.2.1 Stereoelectronic effects on chemical shifts 335

12.2.2 Diamagnetic effects in 1 H NMR 336

12.2.3 Paramagnetic effects in 13C NMR 338

12.2.4 Through -space interactions – γ ]substituent effects 340

12.2.5 Stereoelectronic effects on coupling constants 342

12.3 Conclusion 368

References 368

Index 376