January |
01 |
The Tokuyama Synthesis
of (-)-Histrionicotoxin |
Douglass F. Taber |
08 |
C-O Ring Construction:
The Uchiro Synthesis of GKK1032A2 |
Douglass F. Taber |
15 |
C-O Ring Construction:
Ramariolide B (Sieber), (-)-Hedycoropyran A (Tong), (+)-Colomitide A (Jiao/Xie),
(+)-Laurencin (West), (+)-Laurencin (Widenhoefer/Hong), Chivosazole F
(Paterson) |
Douglass F. Taber |
22 |
C-H Functionalization:
The Inoue Synthesis of Zaragozic Acid C |
Douglass F. Taber |
29 |
Functional Group
Protecting: The Maimone Synthesis of (+)-Mikanokryptin |
Douglass F. Taber |
February |
05 |
The Sato/Chida
Synthesis of Madangamine A |
Douglass F. Taber |
12 |
Enantioselective
Synthesis of Alcohols and Amines: The Hayashi Oxylipin Synthesis |
Douglass F. Taber |
19 |
Enantioselective
Construction of Alkylated Stereogenic Centers: The Nanda Synthesis of
α-Cuparenone |
Douglass F. Taber |
26 |
Arrays of Stereogenic
Centers: The Ellman Synthesis of (+)-Pancratistatin |
Douglass F. Taber |
March |
05 |
The Ma Synthesis of
Lungshengenin D |
Douglass F. Taber |
12 |
Functional Group
Interconversion: The Simpkins Synthesis of Concavine |
Douglass F. Taber |
19 |
Functional Group
Oxidation: The Xie Synthesis of Tochuinyl Acetate |
Douglass F. Taber |
26 |
Functional Group
Reduction |
Douglass F. Taber |
April |
02 |
The Gong/Yang Synthesis
of Pavidolide B |
Douglass F. Taber |
09 |
C-O Ring Construction:
The Carreira Synthesis of (+)-Broussonetine H |
Douglass F. Taber |
16 |
C-O Natural Products:
Leupyrrin B1 (Menche), Polycavernoside A (Sasaki), Intricenyne (Suh),
Toxicodenane A (Ito), Orientalol F (Gong/Yang), Phorbaketal A (Tong) |
Douglass F. Taber |
23 |
C-N Ring Construction:
The Robinson and Morimoto Syntheses of Lepadiformine A |
Douglass F. Taber |
30 |
Alkaloid Synthesis:
Crinine (Tang), Codonopsinine (Jung), Gephyrotoxin 287C (Amat), Kopsone
(Huang/Yu/Hong), Dendrobine (Chen), Actinophyllic Acid (Chen) |
Douglass F. Taber |
May |
07 |
The Fukuyama Synthesis of
Tetrodotoxin |
Douglass F. Taber |
14 |
Reduction: The Beller
Synthesis of Peronatin B |
Douglass F. Taber |
21 |
Oxidation: The Maimone
Synthesis of Majucin |
Douglass F. Taber |
28 |
Organic Functional Group
Conversion: The Gleason Synthesis of Virosaine A |
Douglass F. Taber |
June |
04 |
The Shenvi Synthesis of
(-)-11-O-Debenzoyltashironin |
Douglass F. Taber |
11 |
Functional Group
Protecting: The Rawal Synthesis of (-)-N-Methylwelwitindolinone
B Isothiocyanate |
Douglass F. Taber |
18 |
Substituted Benzene
Derivatives: The Barrett Synthesis of Grifolic Acid |
Douglass F. Taber |
25 |
Heteroaromatics: The Shao/Zhao
Synthesis of Cermizine B |
Douglass F. Taber |
July |
02 |
The Inoue Synthesis of
Resiniferatoxin |
Douglass F. Taber |
09 |
Enantioselective
Synthesis of Alcohols and Amines: The Lindel Synthesis of Hemiasterlin |
Douglass F. Taber |
16 |
Alkylated Stereogenic
Centers: The Cao Synthesis of Chanoclavine I |
Douglass F. Taber |
23 |
Arrays of Stereogenic
Centers: The Wu Synthesis of Neomaclafungin A |
Douglass F. Taber |
30 |
Organocatalyzed C-C Ring
Construction: The Scheidt Synthesis of Armillaridin |
Douglass F. Taber |
August |
06 |
The Dixon Synthesis of
Himalensine A |
Douglass F. Taber |
13 |
Metal-Mediated
Carbocyclic Construction: The Nakada Synthesis of Paclitaxel (Taxol®) |
Douglass F. Taber |
20 |
Diels-Alder
Cycloaddition: Kalihinol C (Shenvi), Lepadin B (Chen), Stachyflin (Magauer),
Antrocin (Su/Yang), Wickerol A (Trauner), Morphine (Chen) |
Douglass F. Taber |
27 |
Carbocyclic
Construction: Lysergine (Luo), Muscone (Yeung), Aplykurodinone-1 (Qiu),
Dendrowardol C (Carreira), Wortmannin (Luo), Aphanamal (Morken) |
Douglass F. Taber |
September |
03 |
The Smith Synthesis
of Nahuoic Acid Ci(Bii) |
Douglass F. Taber |
10 |
Alkene
Functionalization: The Weinreb Synthesis of Alstoscholarisine C |
Douglass F. Taber |
17 |
C-C Bond Formation:
The Hoveyda Synthesis of Prostaglandin E2 |
Douglass F. Taber |
24 |
C-H
Functionalization: The Snyder Synthesis of Scaparvin B |
Douglass F. Taber |
October |
01 |
The Nagorny Synthesis
of Cannogenol and Cannogenol-3-O-α-L-rhamnoside |
Douglass F. Taber |
08 |
Benzene Derivatives:
The Schmidt Synthesis of (+)-Duocarmycin SA |
Douglass F. Taber |
15 |
Heteroaromatic
Construction: The Newhouse Synthesis of (-)-Xylogranatopyridine B |
Dougass F. Taber |
22 |
C-C Bond Construction:
The Mori Synthesis of the Pheromone of the Red-Necked Longhorn Beetle |
Douglass F. Taber |
29 |
Reactions of Alkenes:
The Li Synthesis of Daphenylline |
Douglass F. Taber |
November |
05 |
The Reisman Synthesis
of (+)-Pleuromutilin |
Douglass F. Taber |
12 |
C-N Ring
Construction: The Topczewski Synthesis of Hasubanan |
Douglass F. Taber |
19 |
Alkaloid Synthesis:
Lentiginosine (Orthaber/Samec), Sparteine (Breuning), Pancracine (Cossío),
Akuammiline (Garg), Parvineostemonine (Gaich), Huperzine R (Yokoshima/Fukuyama) |
Douglass F. Taber |
26 |
C-H Functionalization:
The Renata Synthesis of Manzacidin C |
Douglass F. Taber |
December |
03 |
The Shindo Synthesis
of Stemonamine |
Douglass F. Taber |
10 |
Metal-Mediated
Carbocyclic Construction: The Xu Synthesis of Astellatol |
Douglass F. Taber |
17 |
Organocatalyzed
Carbocyclic Construction: The Eichhorn Synthesis of (-)-Ambrox |
Douglass F. Taber |
24 |
Diels-Alder
Cycloaddition: Maoecrystal P (Luo), Sculponin R (Dong), Jerantinine C
(Jiang), Phomoidride D (Wood), Azitine (Ma), Sarcophytin (Carreira) |
Douglass F. Taber |
31 |
Other Methods for
Carbocyclic Construction: Grandisol (Bach), Gracilioether F (Enders/Tang),
Conosilane A (She), ent-Progesterone (Jahn), Spirasine IV (Zhang),
Cyclotrinol (Li) |
Douglass F. Taber |