January |
02 |
The Siegel Synthesis
of Eupalinilide E |
Douglass F. Taber |
09 |
Carbon-Carbon Bond
Formation: The Rhagavan Synthesis of Nupharamine |
Douglass F. Taber |
16 |
C-H Bond
Functionalization: The Vanderwal/Alexanian Synthesis of Chlorolissoclimide |
Douglass F. Taber |
23 |
Flow Methods in
Organic Synthesis |
Douglass F. Taber |
30 |
Organic Functional
Group Interchange: The Wang/Tian/Li Synthesis of Ubiquitin |
Douglass F. Taber |
February |
06 |
The Overman Synthesis
of (-)-Chromodorolide B |
Douglass F. Taber |
13 |
Enantioselective
Synthesis of Alcohols and Amines: The Yakura Synthesis of (+)-Tanikolide |
Douglass F. Taber |
20 |
Alkylated Stereogenic
Centers: The Ceroni/Cozzi Synthesis of (-)-Isodehydroxypodophyllotoxin |
Douglass F. Taber |
27 |
Arrays of Stereogenic
Centers: The Kobayashi/Kogen Synthesis of (-)-L-755,807 |
Douglass F. Taber |
March |
06 |
The Shen/Yang/Hao
Synthesis of Perforanoid A |
Douglass F. Taber |
13 |
Oxidation: The Baran
Synthesis of Nookatone |
Douglass F. Taber |
20 |
Reduction of Organic
Functional Groups |
Douglass F. Taber |
27 |
Functional Group
Protection: The Hudlicky Synthesis of Pleiogenone A |
Douglass F. Taber |
April |
03 |
The Li Synthesis of
Sespenine |
Douglass F. Taber |
10 |
C-O Ring Construction:
The Reber Synthesis of Clerobungin A |
Douglass F. Taber |
17 |
C-O Ring Construction:
Vibralactone (Brown), Obtusallene X (Braddock), Polyrhacitide A (Subba Reddy),
α-Levantenolide (Waymouth/Dai), Macrocidin A (Schobert), Paecilomycin F (Banwell) |
Douglass F. Taber |
24 |
C-N Ring Construction:
The Yang Synthesis of (-)-Alstoscholarisine A |
Douglass F. Taber |
May |
01 |
The Boeckmann Synthesis of
(-)-Nakadomarin A |
Douglass F. Taber |
08 |
Alkaloid Synthesis: (-)-Tashiromine
(Jacobsen), (+)-Neostenine (Sato/Chida), (-)-Sclerotiamide (Sun/Li),
(+)-Minfiensine (Jiao), (+)-Conolidine (Fujii/Ohno), (+)-Peganumine A (Zhu) |
Douglass F. Taber |
15 |
Reduction of Organic
Functional Groups |
Douglass F. Taber |
22 |
Oxidation of Organic
Functional Groups: The Metz Synthesis of (+)-Orientalol F |
Douglass F. Taber |
29 |
Interconversion of Organic
Functional Groups |
Douglass F. Taber |
June |
05 |
The Du Bois Synthesis of
Batrachotoxin |
Douglass F. Taber |
12 |
Functional Group
Protecting: The Li/Wang Synthesis of Ganocin B |
Douglass F. Taber |
19 |
Benzene Derivatives: The
Mohr Synthesis of Ilicicolinic Acid |
Douglass F. Taber |
26 |
Heteroaromatics: The
Cheon Synthesis of Rutaecarpine |
Douglass F. Taber |
July |
03 |
The Zhai Synthesis of
(+)-Harringtonolide |
Douglass F. Taber |
10 |
Enantioselective
Preparation of Alcohols and Amines: The Kalesse Synthesis of Aetheramide A |
Douglass F. Taber |
17 |
Preparation of Alkylated
Stereogenic Centers: The Takayama Synthesis of Kopsiyunnanie K |
Douglass F. Taber |
24 |
Preparation of Arrays of
Stereogenic Centers: The Sudalai Synthesis of (-)-Epiquinamide |
Douglass F. Taber |
31 |
Organocatalyzed C-C Ring
Construction: The Reisman Synthesis of (+)-Psiguadial B |
Douglass F. Taber |
August |
07 |
The Reisman Synthesis
of (+)-Ryanodine |
Douglass F. Taber |
14 |
Metal-mediated
Carbocyclic Construction: The Maimone Synthesis of Berkeleyone A |
Douglass F. Taber |
21 |
Diels-Alder
Cycloaddition: Yaoshanenolide B (Stratakis), 1-Tuberculosinyl Adenosine (Minaard),
penicillone B (Liao), (-)-Neocosmosin A (Cho), Salvinorin (Forsyth),
Dihydroajaconine (Liu/Qin) |
Douglass F. Taber |
28 |
Other Methods for
Carbocyclic Construction: Nigramide R (Donohoe), Aplydactone (Trauner),
Huperzine A (White), Podophyllotoxin (Czarnocki), Strophasterol A (Heretsch),
Jungermannenone B (Lei) |
Douglass F. Taber |
September |
04 |
The Raghavan
Synthesis of Brefeldin A |
Douglass F. Taber |
11 |
Reactions of
Alkenes: The Li Synthesis of Aflavazole |
Douglass F. Taber |
18 |
Carbon-Carbon Bond
Formation: The She Synthesis of Lycopodine |
Douglass F. Taber |
25 |
C-H
Functionalization: The Poulsen Synthesis of Strongylophorine-2 |
Douglass F. Taber |
October |
02 |
The Fukuyama
Synthesis of Morphine |
Douglass F. Taber |
09 |
Substituted Benzenes: The
Reddy Synthesis of Fregenedadiol |
Douglass F. Taber |
16 |
Heterocycle
Construction: The Luo Synthesis of (+)-Lysergol |
Douglass F. Taber |
23 |
Carbon-Carbon Bond
Formation: The Lee Synthesis of Erinacerin A |
Douglass F. Taber |
30 |
Alkene
Functionalization: The Evans Synthesis of Thapsigargin |
Douglass F. Taber |
November |
06 |
The Fan Synthesis of
Palhinine A |
Douglass F. Taber |
13 |
C-N Ring
Construction: The Makabe Synthesis of Isosolenopsin |
Douglass F. Taber |
20 |
Alkaloid Synthesis:
Strictamine (Gaich), Strictamine (Snyder), Corymine (Sun/Li), Lycodoline
(Fan), Mitomycin K (Yang), Lasubine I (Takayama) |
Douglass F. Taber |
27 |
Flow Methods: The
Collins Synthesis of Neomarchantin A |
Douglass F. Taber |
December |
04 |
The Ding Synthesis of
Pharicin A |
Douglass F. Taber |
11 |
Metal-mediated Ring
Construction: The Herzon Synthesis of Pleuromutilin |
Douglass F. Taber |
18 |
Organocatalyzed Ring
Construction: The Lin/Wei Synthesis of δ-Lycorane |
Douglass F. Taber |
25 |
Diels-Alder
Cycloaddition: Sterpuren-4-one (Singh), Kidamycinone (Collet), Magellanine (Barriault),
Cycloclavine (Wipf), Andranginine (Takayama), Illudinine (Dudley) |
Douglass F. Taber |