https://pubs.rsc.org/en/content/articlepdf/2019/NP/C8NP00092A

Marine natural products.

s, or keywords if they used Heck-type chemistry in their syntheses, because it became one of basic tools of organic preparations, a natural way to

http://aether.cmi.ua.ac.be/artikels/Artikels%20Gitte/Artikels/Reviews/Heck%20reactie%20Beletskaya%20%20Chem.%20Rev.%20003009.pdf

The heck reaction as a sharpening stone of palladium catalysis.

Catalytic dehydrogenative cross-coupling: forming carbon-carbon bonds by oxidizing two carbon-hydrogen bonds

Small-molecule H-bond donors in asymmetric catalysis.

4.2.8. Reductive Coupling 3109 5. Reaction of Aromatic Compounds 3110 5.1. Electrophilic Substitutions 3110 5.2. Radical Substitution 3111 5.3. Oxidative Coupling 3111 5.4. Photochemical Reactions 3111 6. Reaction of Carbonyl Compounds 3111 6.1. Nucleophilic Additions 3111 6.1.1. Allylation 3111 6.1.2. Propargylation 3120 6.1.3. Benzylation 3121 6.1.4. Arylation/Vinylation 3121 6.1.5. Alkynylation 3121 6.1.6. Alkylation 3121 6.1.7. Reformatsky-Type Reaction 3122 6.1.8. Direct Aldol Reaction 3122 6.1.9. Mukaiyama Aldol Reaction 3124 6.1.10. Hydrogen Cyanide Addition 3125 6.2. Pinacol Coupling 3126 6.3. Wittig Reactions 3126 7. Reaction of R,â-Unsaturated Carbonyl Compounds 3127

Organic Reactions in Aqueous Media with a Focus on Carbon−Carbon Bond Formations: A Decade Update

Homochiral trans-2-arylcyclohexan-1-ols were synthesized via crude chicken liver esterase (CCLE) mediated enantioselective hydrolysis of the corresponding racemic acetates.

Enzymatic resolution of trans-2-arylcyclohexan-1-ols using crude chicken liver esterase (CCLE) as biocatalyst☆

Application of nitroxy substituent as diastereoface discriminating group in a cyclohexyl based chiral auxiliary has been described.

(1R, 2R)-2-nitroxycyclohexan-1-ol : First example of a cyclohexyl based chiral auxiliary with nitroxy function as diastereoface discriminating group

Enantioselective hydrolysis of racemic acetates of homoallyl alcohols by crude pig liver acetone powder (PLAP)

A simple protocol for the synthesis of a piperidine-2,6-dione framework from Baylis―Hillman adducts

Introduction 8002 1.1. Definition 8003 1.2. Activated alkenes--Michael-type self-dimerization 8005 Intramolecular Baylis-Hillman Reaction 8007 Mechanistic Aspects 8008 3.1. Rate enhancement 8009 3.1.1. Hydrogen bonding 8009 3.1.2. Substrate structure 8010 3.1.3. Pressure, temperature, ultrasound and microwave irradiation 8012 Asymmetric Baylis-Hillman Reaction 8013 4.1. Chiral activated alkenes 8013 4.2. Chiral electrophiles 8016 4.3. Chiral catalysts 8018 4.4. Chiral solvents 8020 4.5. Optical resolution of Baylis-Hillman adducts 8020 4.6. Masked acrylate approach to chiral Baylis-Hillman adducts 8022 Synthetic Applications 8023 5.1. Synthesis of stereodefined alkenes 8023 5.1.1. Stereoselective synthesis of [E]/[Z]-allyl halides and sulphides 8024 5.1.2. Reactions of allylic acetates, halides and sulphides 8026 5.1.2.1. Carbon nucleophiles 8026 5.1.2.2. Hydride as nucleophile 8028 5.1.2.3. Heteroatom-based nucleophiles 8029

Deevi Basavaiah

Papers

Enzymatic resolution of trans-2-arylcyclohexan-1-ols using crude chicken liver esterase (CCLE) as biocatalyst☆

(1R, 2R)-2-nitroxycyclohexan-1-ol : First example of a cyclohexyl based chiral auxiliary with nitroxy function as diastereoface discriminating group

Enantioselective hydrolysis of racemic acetates of homoallyl alcohols by crude pig liver acetone powder (PLAP)

A simple protocol for the synthesis of a piperidine-2,6-dione framework from Baylis―Hillman adducts

The Baylis-Hillman Reaction: A Novel Carbon-Carbon Bond Forming Reaction