January |
06 |
The Sarpong Synthesis of Ambiguine P |
Douglass F. Taber |
13 |
C-O Ring Construction:
The Jeong/Shin Syntheses of Giffonin H |
Douglass F. Taber |
20 |
C-O Ring Construction:
Vancosamine (Gademann), Scleropentaside A (Schützenmeister), Monocerin (Ghosh),
Obolactone (Fernandes), Caseabalansin A (Sugita), Rhizoxin D (Fürstner) |
Douglass F. Taber |
27 |
Functional Group
Interconversion: The Raghavan synthesis of Solandelactone F |
Douglass F. Taber |
February |
03 |
The Carreira
Synthesis of Merochlorin A |
Douglass F. Taber |
10 |
Enantioselective
Synthesis of Alcohols and Amines: The You Synthesis of Chelonin A |
Douglass F. Taber |
17 |
Construction of
Alkylated Centers: The Zu Synthesis of Aflatoxin B2 |
Douglass F. Taber |
24 |
Arrays of Stereogenic
Centers: The Hu Synthesis of Ileabethoxazole |
Douglass F. Taber |
March |
02 |
The Christmann Synthesis
of Darwinolide |
Douglass F. Taber |
09 |
Oxidation: The Micalizio
Route to the Corialactones |
Douglass F. Taber |
16 |
Reduction: The Xu
Synthesis of Himalensine A |
Douglass F. Taber |
23 |
Functional Group
Protecting: The Newhouse Synthesis of Principinol D |
Douglass F. Taber |
30 |
Preparative Enzymatic
Synthesis of Carbocycles: Cembranolide (Taber), Quassin (Shing), Wickerol A
(Gui), Cattyleyene (Dickschat), Englerin A (Liu/Christmann), Artemisinic
Acid (Paddon/Newman), Etoposide Aglycone (Satteley) |
Douglass F. Taber |
April |
06 |
The Sarlah Synthesis
of Stelletin E |
Douglass F. Taber |
13 |
C-N Ring Construction:
Septicine (Kleij) and Gelsemolenine A (Takayama) |
Douglass F. Taber |
20 |
Alkaloid Synthesis:
Lentiginosine (Repo/Samec), (+)-Quinine (Ishikawa), Lasubine II (Pansare),
Naucleofficine I (Tu), Vindorosine (Ohno), Taberdivarine H (Poupon/Vincent/Evanno) |
Douglass F. Taber |
27 |
Carbon-Carbon Bond
Formation: The Burtoloso Synthesis of Brussonol |
Douglass F. Taber |
May |
04 |
The Inoue Synthesis of
1-Hydroxytaxinine |
Douglass F. Taber |
11 |
C-O Ring Construction: The
Silipo/Yu Synthesis of Forsythenethoside A |
Douglass F. Taber |
18 |
C-O Ring Construction:
Coriolide (Fernandes), Monocillin VII (Mohapatra), Diplobifuranylone B
(Zhang), Diocolletines A (Kuwahara), Griseusin A (Thorson/She), Galanthamine
(Zhang/Tu) |
Douglass F. Taber |
25 |
Reactions of Alkenes: The
Breit Synthesis of Vermiculine |
Douglass F. Taber |
June |
01 |
The Snyder Synthesis of
Conidiogenone |
Douglass F. Taber |
08 |
Benzene Derivatives: The
Chen Synthesis of Glabralide B |
Douglass F. Taber |
15 |
Heteroaromatics: The
Zhang Synthesis of Suaveoline |
Douglass F. Taber |
22 |
C-H Functionalization:
The Borhan Synthesis of Salinosporamide A |
Douglass F. Taber |
29 |
Functional Group
Interconversion: The Cordero-Vargas Synthesis of Aspergillide A |
Douglass F. Taber |
July |
06 |
The Li Synthesis of
Vinigrol |
Douglass F. Taber |
13 |
Enantioselective
Synthesis of Alcohols and Amines: The Menche Synthesis of Tuscoron D |
Douglass F. Taber |
20 |
Alkylated Stereogenic
Centers: The Lei/Kong Synthesis of Esermethole |
Douglass F. Taber |
27 |
Arrays of Stereogenic
Centers: The Ishikawa Synthesis of Secologanin |
Douglass F. Taber |
August |
03 |
The Reisman Synthesis
of Perseanol |
Douglass F. Taber |
10 |
Metal-Mediated C-C Ring
Construction: The Harada/Nemoto Synthesis of Catharanthine |
Douglass F. Taber |
17 |
Organocatalyzed C-C
Ring Construction: The Takakawa Synthesis of Salinipostin A |
Douglass F. Taber |
24 |
Diels-Alder
Cycloaddition: Pericoannosin A (Lindsley), Arborone (Corey),
Furoerioaustralasine (George), Liangshanin G (Ma), Arcutinidine (Sarpong),
Mitrephorone A (Magauer) |
Douglass F. Taber |
31 |
Other Methods for
Carbocyclic Construction: Pentalenonelactone A Methyl Ester (Chuang),
Atlanticone C (Bach), Aquatolide (Takao), Incarviatone A (Sarpong), Oridonin
(Luo), Illisimonin A (Rychnovsky) |
Douglass F. Taber |
September |
07 |
The Ohtawa/Shenvi
Synthesis of Bilobalide |
Douglass F. Taber |
14 |
Oxidation: The Khan
Synthesis of Iridomyrmecin |
Douglass F. Taber |
21 |
Reduction: The
Kobayashi Synthesis of Bromlaurenidificin |
Douglass F. Taber |
28 |
Functional Group
Protection: The Renaud Synthesis of Brefeldin C |
Douglass F. Taber |
October |
05 |
The Luo Synthesis of
Batrachotoxinin A |
Douglass F. Taber |
12 |
Substituted Benzenes:
The Fujiwara Synthesis of Selaginellin A |
Douglass F. Taber |
19 |
Heteroaromatics: The
Pritchard/Kimber Synthesis of 11D5(F6) |
Douglass F. Taber |
26 |
C-H Functionalization:
The Yang Synthesis of Fennebricin A |
Douglass F. Taber |
November |
02 |
The Baran
Synthesis of Paclitaxel (Taxol®) |
Douglass F. Taber |
09 |
C-N Ring
Construction: The Kürti Synthesis of N-Methyl Euphococcine |
Douglass F. Taber |
16 |
Alkaloid Synthesis:
Julifloridine (Huang), γ-Lycorane (Wang/Huang), Lycojaponicumin A
(Zhang/Tu), Isatindigotindoline C (Siitonen/Kürti), Curvulamine (Maimone),
Kopsifoline D (Peng) |
Douglass F. Taber |
23 |
Reactions of Alkenes:
The Christmann Synthesis of Spongidine A |
Douglass F. Taber |
30 |
Diels-Alder Cycloaddition:
Prostaglandin E2 (Kagan), Pseudopterosin (-)-G-J aglycone (Vanderwal),
Lyconadin D (Yang), Spruceanol (Xue), Scabrolide A (Stoltz) |
Douglass F. Taber |
December |
07 |
The Yokoshima
Synthesis of Tetrodotoxin |
Douglass F. Taber |
14 |
Metal-Mediated C-C
Ring Construction: The Trost Synthesis of Conocenolide C |
Douglass F. Taber |
21 |
Organocatalyzed Carbocyclic Ring
Construction: The Appayee Synthesis of 9β-11-Hydroxyhexahydrocannabinol |
Douglass F. Taber |
28 |
Other Methods for
Carbocyclic Construction: Aspidodispermine (Heretsch), Lepadiformine A (Tokuyama),
Farnesin (Gao), Ganocin B (Zhao), Dankasterone B (Heretsch),
Canataxpropellane (Gaich) |
Douglass F. Taber |