| January |
| 02 |
The Li Synthesis of
Albolic Acid |
Douglass F. Taber |
| 09 |
C-O Ring Construction:
The Fuwa Synthesis of Exiguolide |
Douglass F. Taber |
| 16 |
C-O Ring Construction:
Ophiofuranone A (Schobert), Galanthamine (Brown), Spirooliganone A (Morita),
Microansamycin H (Sittihan), Gymnothelignan N (Lee), 3(11)-Epoxyhypoestenone
(Wang/Chen) |
Douglass F. Taber |
| 23 |
Reactions of Alkenes:
The Chida Synthesis of Paclitaxel (TaxolŽ) |
Douglass F. Taber |
| 30 |
Functional Group
Interconversion: The Salom-Roig Synthesis of α-Conhydrine |
Douglass F. Taber |
| February |
| 06 |
The Ding Synthesis of
Crinipellin F |
Douglass F. Taber |
| 13 |
Enantioselective
Synthesis of Alcohols and Amines: The Huang/Chen Synthesis of α-Tocopherol |
Douglass F. Taber |
| 20 |
Enantioselective
Construction of Alkylated Stereogenic Centers: The Bisai Synthesis of
Lycoramine |
Douglass F. Taber |
| 27 |
Arrays of Stereogenic
Centers: The Liu Synthesis of Shizukaol J |
Douglass F. Taber |
| March |
|
|
| 06 |
The Luo Synthesis of
Triptonide |
Douglass F. Taber |
| 13 |
Oxidation: The Vanderwal
Synthesis of 7,20-Diisocyanoadociane |
Douglass F. Taber |
| 20 |
Reduction: The Odagi/Nagasawa
Synthesis of Cepharatine A |
Douglass F. Taber |
| 27 |
Functional Group
Protection: The Pronin Synthesis of Quassin |
Douglass F. Taber |
| April |
| 03 |
The Dai Synthesis of
Peyssonnoside A |
Douglass F. Taber |
| 10 |
C-N Ring Construction: The
Louie Synthesis of Septicine |
Douglass F. Taber |
| 17 |
Alkaloid Synthesis:
Tabertinggine (She), Kopisinine (Ruijter), Sieboldine A (Yao), Rhazinicine
(Miranda), Brevianamide A (Gagosz), Daphlongamine E (Xu) |
Douglass F. Taber |
| 24 |
C-H Functionalization: The
Zhu Synthesis of β-Cuparenone |
Douglass F. Taber |
| May |
| 01 |
The Zhao/Ma Synthesis of
Napelline |
Douglass F. Taber |
| 08 |
C-O Ring Construction: The
Liu/Wang Synthesis of Miharimycin B |
Douglass F. Taber |
| 15 |
C-O Ring Construction:
Spiroapplanatumine O (Jahn), Alcyonolide (Hosokawa), Wentilactone A (Xu/Yu),
Aquilanol A (Stathakis), Thallusin (Arndt), Neobraclactone C (Cheng/Liu) |
Douglass F. Taber |
| 22 |
Reactions of Alkenes: The
Tanino Synthesis of 2-Isocyanoallopupukeanane |
Douglass F. Taber |
| 29 |
C-C Bond Construction: The
Li/She Synthesis of Pharbilinic Acid |
Douglass F. Taber |
| June |
| 05 |
The Trauner Synthesis of
Tetrodotoxin |
Douglass F. Taber |
| 12 |
Benzene Derivatives: The
Dudley Synthesis of Coprinol |
Douglass F. Taber |
| 19 |
Heteroaromatics: The Wei/Zu
Synthesis of Gilbertine |
Douglass F. Taber |
| 26 |
Functional Group
Interconversion: The Hirose/Sunazuka Synthesis of Luminamicin |
Douglass F. Taber |
| July |
| 03 |
The Carreira Synthesis of
Aberrarone |
Douglass F. Taber |
| 10 |
Enantioselective Synthesis
of Alcohols and Amines: The Zhang/Tu Synthesis of Eupomatilone-6 |
Douglass F. Taber |
| 17 |
Alkylated Stereogenic
Centers: The Zakarian Synthesis of Goniomitine |
Douglass F. Taber |
| 24 |
Arrays of Stereogenic
Centers: The Tanaka/Kitamura Synthesis of Pancratistatin |
Douglass F. Taber |
| 31 |
Organocatalyzed C-C Ring
Construction: The Takao Synthesis of Puraquinonic Acid |
Douglass F. Taber |
| August |
| 07 |
The Barriault Synthesis
of Ginkgolide C |
Douglass F. Taber |
| 14 |
Metal-mediated C-C Ring
Construction: The Sarpong Synthesis of 15-Hydroxypatchoulol |
Douglass F. Taber |
| 21 |
Diels-Alder
Cycloaddition: Rameswaralide (Romo), Lucidumone (de la Torre), Anthracimycin
(Qian/Tong), Alstonlarsine A (Ferjancic/Bihelovic), Ophiorrine A (Vincent),
Daphgraciline (Sun/Li) |
Douglass F. Taber |
| 28 |
Other Methods for
Carbocyclic Construction: 6,11-Epoxyisodaucane (Tanino), Magellanine (Yao),
Nemorosonol (Ohyoshi/Kigoshi), Antroalbocin (Kalesse), Cochlearol B
(Schindler), Emerione A (Miller) |
Douglass F. Taber |
| September |
| 04 |
The Renata Synthesis
of Gedunin |
Douglass F. Taber |
| 11 |
Oxidation: The Hong/Gui
Synthesis of Bufospirostenin A |
Douglass F. Taber |
| 18 |
Reduction: The
Ichikawa/Hosokawa Synthesis of Axisonitrile-3 |
Douglass F. Taber |
| 25 |
Functional Group
Protection: The Carreira/Piel Synthesis of Janustatin A |
Douglass F. Taber |
| October |
| 02 |
The Garg Synthesis of
Lissodendoric Acid A |
Douglass F. Taber |
| 09 |
Substituted Benzenes:
The Newhouse Synthesis of Shearilicine |
Douglass F. Taber |
| 16 |
Heteroaromatics: The Zhu
Synthesis of Anibamine B |
Douglass F. Taber |
| 23 |
Carbon-Carbon Bond
Formation: The Kalesse Synthesis of Illisimonin A |
Douglass F. Taber |
| 30 |
C-H Functionalization:
The Gui Synthesis of Phomarol |
Douglass F. Taber |
| November |
| 06 |
The Jia Synthesis of
Aberrarone |
Douglass F. Taber |
| 13 |
C-N Ring Construction:
The Hayashi Synthesis of Quinine |
Douglass F. Taber |
| 20 |
Alkaloid Synthesis:
Indolizidine 209D (Qiu/He/Zhang), Kopsone (Yokoshima), Quinocarcin (Zheng/Huang),
Daphnillonin B (Li), Daphnezomine B (Zhai), Vilmoraconitine (Liu/Qin) |
Douglass F. Taber |
| 27 |
Organocatalyzed C-C
Ring Construction: The Ikeuchi/Tanino Synthesis of Coriamytrin |
Douglass F. Taber |
| December |
| 04 |
The Chen/Wang
Synthesis of Retigeranic Acid |
Douglass F. Taber |
| 11 |
Metal-Mediated C-C Ring
Construction: The Li Synthesis of Bufogargarizin A |
Douglass F. Taber |
| 18 |
Diels-Alder
Cycloaddition: δ-Cadinol (Schulz), KB343 (Baran), Penostatin C (Chen),
Senopodine E (Ishikawa), Vermisporin (Lei), Kibdelomycin (Schobert) |
Douglass F. Taber |
| 25 |
Other Methods for C-C
Ring Construction: Scabrolide A (Sarlah), Clovan-2,9-dione (Newhouse),
Gibberellin A18 (Dai), Isoneoamphilectane (Vanderwal), Stelletin E (Jiao/Xie),
Puberuline C (Inoue) |
Douglass F. Taber |
