| January |
| 01 |
The Fan Synthesis of
Trachinol |
Douglass F. Taber |
| 08 |
C-O Ring Construction:
The Menche Synthesis of Pentamycin |
Douglass F. Taber |
| 15 |
C-O Ring Construction:
Petromyroxol (Fernandes), Hedyosumin A (Chen/Yang), Cephalosporolide J (Ota/Miyaoka),
Malettenin C (Yokoshima), xyloketal B (Narayan), Lucidumone (Kawamoto/Ito) |
Douglass F. Taber |
| 22 |
Reduction: The Tadpetch
Synthesis of Pestalotioprolide B |
Douglass F. Taber |
| 29 |
Oxidation: The Frantz
Route to Artemisinin |
Douglass F. Taber |
| February |
| 05 |
The Suzuki/Tanino
Synthesis of Kamebanin |
Douglass F. Taber |
| 12 |
Enantioselective
Synthesis of Alcohols and Amines: The Lin/Liu Route to Haliclamide |
Douglass F. Taber |
| 19 |
Alkylated Stereogenic
Centers: The Tambar Synthesis of Enterolactone |
Douglass F. Taber |
| 26 |
Arrays of Stereogenic
Centers: The Wei/Yang Synthesis of Cephalotaxine |
Douglass F. Taber |
| March |
|
|
| 04 |
The Baran Synthesis of
Cyclopamine |
Douglass F. Taber |
| 11 |
Functional Group
Interconversion: The Nagasawa/Iwabuchi Synthesis of Rumphellclovane E |
Douglass F. Taber |
| 18 |
Functional Group
Protection: The White Synthesis of Usaramine |
Douglass F. Taber |
| 25 |
Reactions of Alkenes: The
Wood Synthesis of Alterbrassicicene C |
Douglass F. Taber |
| April |
| 01 |
The White/Banwell/Lan
Synthesis of Codeine |
Douglass F. Taber |
| 08 |
C-N Ring Construction: The
Wang/Huo/Zong Synthesis of Flustramine B |
Douglass F. Taber |
| 15 |
Alkaloid Synthesis:
Hinckdentine A (Rawal), Isolycoricidine (Canesi), Normacusine B (Qi),
Silicine (Ishikawa), Cephalocyclidin A (Zhang/Tu), Alstolucine B (Lan/Zhang) |
Douglass F. Taber |
| 22 |
C-H Functionalization: The
Wei/Yang Synthesis of Cephalotine A |
Douglass F. Taber |
| 29 |
Carbon-Carbon Bond
Formation: The Aggarwal Synthesis of 10-Deoxymethynolide |
Douglass F. Taber |
| May |
| 06 |
The Inoue Synthesis of
Batrachotoxin |
Douglass F. Taber |
| 13 |
C-O Ring Construction: The
Feng/Liu Synthesis of Goniochelienactone |
Douglass F. Taber |
| 20 |
C-O Ring Construction:
Cephalasporolide F (Sartillo-Piscil), Hedycoropyran A (Kim/Lee),
Applanatumol A (Ito), Lycibarbarine C (Liu/Du), Goniofufurone (Makabe),
Angustatin A (Alcarazo) |
Douglass F. Taber |
| 27 |
Reactions of Alkenes: The
Shenvi Synthesis of Eugenial C |
Douglass F. Taber |
| June |
| 03 |
The Baran Synthesis of
Portimine B |
Douglass F. Taber |
| 10 |
Benzene Derivatives: The
Guo Synthesis of Fumimycin |
Douglass F. Taber |
| 17 |
Heteroaromatics: The Šačus/Opatz
Synthesis of Lamellarin G Trimethyl Ether |
Douglass F. Taber |
| 24 |
Functional Group
Interconversion: The Maier Synthesis of Berkeylactone A |
Douglass F. Taber |
| July |
| 01 |
The Ding Synthesis of
Vulgarisin A |
Douglass F. Taber |
| 08 |
Enantioselective Synthesis
of Alcohols and Amines: The Fernandes Synthesis of Diosniponol A |
Douglass F. Taber |
| 15 |
Alkylated Stereogenic
Centers: The Romiti Synthesis of Eburnamenine |
Douglass F. Taber |
| 22 |
Arrays of Stereogenic
Centers: The Hajra Synthesis of Podophyllotoxin |
Douglass F. Taber |
| 29 |
Organocatalyzed C-C Ring
Construction: The Xiang Synthesis of Isoagatholactone |
Douglass F. Taber |
| August |
| 05 |
The Yang Synthesis of
Illisimonin A |
Douglass F. Taber |
| 12 |
Metal-Mediated C-C Ring
Construction: The Ota/Miyaoka Synthesis of Saniculamoid D |
Douglass F. Taber |
| 19 |
Diels-Alder
Cycloaddition: Fawcettimine (Yokoshima), Teucvin (Cai), Phleghenrine A
(Dai), 1-Deacetylcaesalmin C (Carreira), Pedrolide (Carreira), Orientanoid A
(Ai/Fan/Yue) |
Douglass F. Taber |
| 26 |
Other Methods for
Carbocyclic Construction: Agelastatin A (Afonso/Siopa), Sculponin U (Fu/Liu),
Artatrovirenol A (Zhu), Methyl Phomopsenoate (Shi/Hou/Tu), Euphol (Micalizio) |
Douglass F. Taber |
| September |
| 02 |
The Shenvi Synthesis
of Cotylenol |
Douglass F. Taber |
| 09 |
Functional Group
Protection: The Meepowan Synthesis of Protoconstipatic Acid Methyl Ester |
Douglass F. Taber |
| 16 |
Functional Group
Oxidation: The Liu/Du Synthesis of Varioxiranol B |
Douglass F. Taber |
| 23 |
Reduction: The
Barriault Synthesis of Salvinorin A |
Douglass F. Taber |
| 30 |
The Logothetis
Reaction: Solenopsin B (Taber), Swaisonine (Cha), Indolizidine 223AB (Taber),
Quinolizidine 217A (Pearson), FR66979 (Ciufolini) |
Douglass F. Taber |
| October |
| 07 |
The Huang/Yang
Synthesis of Penicibilaene A |
Douglass F. Taber |
| 14 |
Substituted Benzenes:
The Tsukano Synthesis of Lancilactone C |
Douglass F. Taber |
| 21 |
Heteroaromatics: The
Scheerer Synthesis of Rupestine M |
Douglass F. Taber |
| 28 |
C-C Bond Formation: The
Ichikawa/Hosokawa Synthesis of Halichonadin B |
Douglass F. Taber |
| November |
| 04 |
The Liu/Qin Synthesis of
Cyclopamine |
Douglass F. Taber |
| 11 |
C-N Ring Construction:
The Song/Qin Synthesis of Mitragynine |
Douglass F. Taber |
| 18 |
Alkaloid Synthesis:
Allokainic acid (Tilve), Preussin (Ryu), Toussaintine C (Hayakawa),
Powelline (Tang), Arborduridine (Ma), Securine A (Herzon) |
Douglass F. Taber |
| 25 |
C-H Functionalization:
The Li/She Synthesis of Pepluacetal |
Douglass F. Taber |
| December |
| 02 |
The Qi Synthesis of
Tetrodotoxin |
Douglass F. Taber |
| 09 |
Metal-Mediated C-C Ring
Construction: The Liu/Qin Synthesis of Garryine |
Douglass F. Taber |
