| January |
| 04 |
The Williams Synthesis of (-)-4-Hydroxydictyolactone |
Douglass F. Taber |
| 11 |
Advances in Alkene
Metathesis: The Hoveyda Synthesis of (+)-Quebrachamine |
Douglass F. Taber |
| 18 |
Alkene and Alkyne
Metathesis: Navenone B (Cossy), (+)-Asperpentyn (Daesung Lee), (-)-Amphidinolide
K (Eun Lee), Norhalichondrin B (Phillips) |
Douglass F. Taber |
| 25 |
Enantioselective
Preparation of Alcohols and Amines: The Suh Synthesis of (-)-Macrosphelide J |
Douglass F. Taber |
| February |
| 01 |
The Nakada Synthesis
of (-)-FR182877 |
Douglass F. Taber |
| 08 |
Enantioselective
Construction of Alkylated Centers: The Maier Synthesis of Platencin |
Douglass F. Taber |
| 15 |
Construction of
Arrays of Stereogenic Centers: The Zhang Synthesis of (+)-Podophyllotoxin |
Douglass F. Taber |
| 22 |
Best Synthetic
Methods: Reduction |
Douglass F. Taber |
| March |
| 01 |
The Trost Synthesis of
(-)-Pseudolaric Acid B |
Douglass F. Taber |
| 08 |
Best Synthetic Methods:
Oxidation |
Douglass F. Taber |
| 15 |
Organic Functional Group
Protection |
Douglass F. Taber |
| 22 |
New Methods for
Carbon-Carbon Bond Construction |
Douglass F. Taber |
| 29 |
Best Synthetic Methods:
Reactions of Alkenes |
Douglass F. Taber |
| April |
| 05 |
The Corey Synthesis of
(+)-Lupeol |
Douglass F. Taber |
| 12 |
Stereoselective C-O Ring
Construction: The Jamison Synthesis of (-)-Gloeosporone |
Douglass F. Taber |
| 19 |
Synthesis of
Naturally-Occurring Cyclic Ethers: Boivivianin B (Murakami), SC-Δ13-9-IsoF
(Taber), Brevisamide (Panek, Lindsley, Ghosh), Gambierol (Mori) |
Douglass F. Taber |
| 26 |
Stereocontrolled C-N
Ring Construction: The Takayama Synthesis of Lycoposerramine-C |
Douglass F. Taber |
| May |
| 03 |
The Dixon Synthesis of (-)-Nakadomarin
A |
Douglass F. Taber |
| 10 |
Alkaloid Synthesis: (S)-Nicotine
(Helmchen), (+)-CP-99,994 (Shi), (-)-Adaline (Yu), (-)-Securinine (Bayón/Figueredo),
Alkaloid 223A (Aubé), (-)-Huperzine A (Fukuyama) |
Douglass F. Taber |
| 17 |
Best Synthetic Methods:
Functional Group Transformations |
Douglass F. Taber |
| 24 |
Best Synthetic Methods:
Oxidation and Reduction |
Douglass F. Taber |
| 31 |
Best Synthetic Methods:
C-C Bond Construction |
Douglass F. Taber |
| June |
| 07 |
The Magnus Synthesis of
(±)-Codeine |
Douglass F. Taber |
| 14 |
Benzene Derivatives: The
Tanino-Miyashita Synthesis of Zoanthenol |
Douglass F. Taber |
| 21 |
Heteroaromatic
Construction: The Jia Synthesis of (-)-cis-Clavicipitic Acid |
Douglass F. Taber |
| 28 |
Progress in Alkene and
Alkyne Metathesis: (+)-5-epi-Citreoviral (Funk) and (±)-Poitediol
(Vanderwal) |
Douglass F. Taber |
| July |
| 05 |
The Nicolaou Synthesis of
(+)-Hirsutellone B |
Douglass F. Taber |
| 12 |
Enantioselective
Preparation of Alcohols and Amines |
Douglass F. Taber |
| 19 |
Enantioselective
Construction of Alkylated Stereogenic Centers |
Douglass F. Taber |
| 26 |
Enantioselective
Construction of Arrays of Stereogenic Centers: The Breit Synthesis of (+)-Bourgeanic
Acid |
Douglass F. Taber |
| August |
| 02 |
The Nicolaou Synthesis
of (+)-Vannusal |
Douglass F. Taber |
| 09 |
Metal-Mediated Carbocyclic Construction:
The Kobayashi Synthesis of (+)-Fomitellic Acid B |
Douglass F. Taber |
| 16 |
Organocatalytic
Carbocyclic Construction: The Christmann Synthesis of (+)-Rotundial |
Douglass F. Taber |
| 23 |
Carbocyclic
Construction: The Deng Synthesis of (-)-Plicatic Acid |
Douglass F. Taber |
| 30 |
Tethered Diels-Alder
Cycloaddition: (±)-Neovibsanin B (Imagawa, Nishizawa), Valerenic Acid (Mulzer),
(-)-Himandrine (Movassaghi), (±)-Pallavicinolide A (Wong), (+)-Phomopsidin (Nakada) |
Douglass F. Taber |
| September |
| 06 |
The Baran Synthesis
of Vinigrol |
Douglass F. Taber |
| 13 |
Functional Group
Protection: The Kraus Synthesis of Bauhinoxepin J |
Douglass F. Taber |
| 20 |
Alkene Reactions:
The Dabdoub/Baroni Synthesis of (±)-Dihydroactinidiolide |
Douglass F. Taber |
| 27 |
C-H
Functionalization: The White Synthesis of 6-Deoxyerythronolide B |
Douglass F. Taber |
| October |
| 04 |
The Overman Synthesis
of Briarellin F |
Douglass F. Taber |
| 11 |
Substituted Benzenes:
The Saikawa/Nakata Synthesis of Kendomycin |
Douglass F. Taber |
| 18 |
Heteroaromatics: The
Mal Synthesis of Clausevatine D |
Douglass F. Taber |
| 25 |
Functional Group
Transformation: The Castle Synthesis of Celogentin C |
Douglass F. Taber |
| November |
| 01 |
The Shair
Synthesis of Cephalostatin 1 |
Douglass F. Taber |
| 08 |
Functional Group
Protection |
Douglass F. Taber |
| 15 |
Stereocontrolled C-N
Ring Construction: The Pyne Synthesis of Hyacinthacine B3 |
Douglass F. Taber |
| 22 |
Synthesis of C-N
Natural Products: (-)-α-Kainic Acid (Helmchen), (+)-Tylophorine (Opatz), (-)-Lycoperine
A (Rychnovsky), Fluvirucidine A2 (Suh), Complanidine A (Sarpong) |
Douglass F. Taber |
| 29 |
Stereocontrolled
Construction of C-O Rings: The Seeberger/Hilvert Synthesis of KDN |
Douglass F. Taber |
| December |
| 06 |
The Chen Synthesis of
(-)-Nakiterpiosin |
Douglass F. Taber |
| 13 |
Transition-Metal
Catalyzed Ring Construction: The Yu Synthesis of α-Agorafuran |
Douglass F. Taber |
| 20 |
Enantioselective
Organocatalytic C-C Ring Construction |
Douglass F. Taber |
| 27 |
New Methods for
Carbocyclic Construction: The Kim Synthesis of Pentalenene |
Douglass F. Taber |
