:Staudinger synthesis

The reaction was discovered in 1907 by the German chemist Hermann Staudinger.{{cite journal | author = H. Staudinger | journal = Justus Liebigs Ann. Chem. | year = 1907 | volume = 356 | issue = 1–2 | pages = 51–123 | doi = 10.1002/jlac.19073560106 | title = Zur Kenntniss der Ketene. Diphenylketen| url = https://zenodo.org/record/1427571 }} The reaction did not attract interest until the 1940s, when the structure of penicillin was elucidated. The β-lactam moiety of the first synthetic penicillin was constructed using this cycloaddition,{{cite journal | author = J.C. Sheehan, E.L. Buhle, E.J. Corey, G.D. Laubach, J.J. Ryan | journal = J. Am. Chem. Soc. | year = 1950 | volume = 72 | pages = 3828–9 | doi = 10.1021/ja01164a534 | issue = 8 | title = The Total Synthesis of a 5-Phenyl Penicillin: Methyl 5-Phenyl-(2-Carbomethoxyethyl)-Penicillinate}} and it remains a valuable tool in synthetic organic chemistry.

The first step is a nucleophilic attack by the imine nitrogen on the carbonyl carbon to generate a zwitterionic intermediate. Electron-donating groups on the imine facilitate this step, while electron-withdrawing groups impede the attack.{{cite book|editor1-last=Li|editor2-last=Jie Jack|title=Name Reactions for Carbocyclic Ring Formations|year=2010|publisher=Wiley|location=Hoboken, N.J.|isbn=9780470872208|page=47}} The second step is either an intramolecular nucleophilic ring closure or a conrotatory electrocyclic ring closure.{{cite journal |last1=Qi |first1=Hengzhen |last2=Li |first2=Xinyao |last3=Xu |first3=Jiaxi |date=December 2010 |title= Stereoselective control in the Staudinger reactions involving monosubstituted ketenes with electron acceptor substituents: experimental investigation and theoretical rationalization |journal=Organic and Biomolecular Chemistry |volume=9 |issue= 8|pages=2702–2714 |doi=10.1039/C0OB00783H|pmid=21359284 |s2cid=37085450 }} The second step is different from typical electrocyclic ring closures as predicted by the Woodward–Hoffmann rules. Under photochemical and microwave conditions the intermediate's 4π-electron system cannot undergo a disrotatory ring closure to form the β-lactam, possibly because the two double bonds are not coplanar.{{cite journal |last1=Liang |first1=Yong |last2=Jiao |first2=Lei |last3=Zhang |first3=Shiwei |last4=Xu |first4= Jiaxi |date=2005 |title= Microwave- and Photoirradiation-Induced Staudinger Reactions of Cyclic Imines and Ketenes Generated from α-Diazoketones. A Further Investigation into the Stereochemical Process |journal=Journal of Organic Chemistry |volume=70 |issue=1 |pages=334–337 |doi=10.1021/jo048328o|pmid=15624943 }} Some products of the Staudinger synthesis differ from those predicted by the torquoelectronic model.{{cite journal |last1=Jiao |first1=Lei |last2=Liang |first2=Yong |last3=Xu |first3= Jiaxi |date=2006 |title=Origin of the Relative Stereoselectivity of the β-Lactam Formation in the Staudinger Reaction |journal=Journal of the American Chemical Society |volume=128 |issue=18 |pages=6060–6069 |doi=10.1021/ja056711k|pmid=16669675 }} In addition, the electronic structure of the transition state differs from that of other conrotary ring closures.

There is evidence from computational studies on model systems that in the gas phase the mechanism is concerted.

File:Staudinger-Synthese_RM2.svg

The stereochemistry of the Staudinger synthesis can be difficult to predict because either step can be rate-determining.{{cite journal |last1=Liang |first1=Yong |last2=Jiao |first2=Lei |last3=Zhang |first3= Shiwei |last4=Yu |first4= Zhi-Xiang |last5= Xu |first5= Jiaxi |date=2009 |title=New Insights into the Torquoselectivity of the Staudinger Reaction |journal=Journal of the American Chemical Society |volume=131 |issue=4 |pages=1542–1549 |doi=10.1021/ja808046e|pmid=19132931 }} If the ring closure step is rate-determining, stereochemical predictions based on torquoselectivity are reliable. Other factors that affect the stereochemistry include the initial regiochemistry of the imine. Generally, (E)-imines form cis β-lactams while (Z)-imines form trans β-lactams. Other substituents affect the stereochemistry as well. Ketenes with strong electron-donating substituents mainly produce cis β-lactams, while ketenes with strong electron-withdrawing substituents generally produce trans β-lactams. The ketene substituent affects the transition state by either speeding up or slowing down the progress towards the β-lactam. A slower reaction allows for the isomerization of the imine, which generally results in a trans product.

File:Staudinger-Synthese_Stereochemie_V3.svg

Reviews on asymmetric induction of the Staudinger synthesis, including the use of organic and organometallic catalysts, have been published.{{cite journal |last1=Palomo |first1=Claudio |last2= Aizpurua |first2=Jesus M. |last3=Ganboa |first3=Iñaki |last4=Oiarbide |first4=Mikel |date=1999 |title=Asymmetric Synthesis of β-Lactams by Staudinger Ketene-Imine Cycloaddition Reaction |journal=European Journal of Organic Chemistry |volume=1999 |issue=12 |pages=3223–3235 |doi=10.1002/(SICI)1099-0690(199912)1999:12<3223::AID-EJOC3223>3.0.CO;2-1 }}

The imine can be replaced by adding olefin to produce a cyclobutanone, carbonyl to produce a β-lactone, or carbodiimides to produce 4-imino β-lactams. The Staudinger synthesis and variations are all ketene cycloadditions.

File:Staudinger-Synthese_Variationen_V3.svg

In 2014, Doyle and coworkers reported a one-pot, multicomponent Staudinger synthesis of β-lactams from azides and two diazo compounds. The reaction occurs by a rhodium acetate-catalyzed reaction between the aryldiazoacetate (red) and the organic azide (blue) to form an imine. A Wolff rearrangement of the diazoacetoacetate enone (black) forms a stable ketene, which reacts with the imine to form a stable β-lactam compound. The solvent used for this reaction is dichloromethane (DCM) and the solution needs to rest for 3 hours at room temperature. The yield of the reaction is about 99%.{{cite journal |last1=Mandler |first1=Michael D. |last2= Truong |first2=Phong M. |last3=Zavalij |first3=Peter Y. |last4=Doyle |first4=Michael P. |date=2014 |title=Catalytic Conversion of Diazocarbonyl Compounds to Imines |journal=Organic Letters |volume=16 |issue=3 |pages=740–743 |doi=10.1021/ol403427s|pmid=24423056 }}

File:Staudinger-Synthese Eintopfreaktion V8.svg

The reaction with sulfenes instead of ketenes leading to β-sultams is called Sulfa-Staudinger cycloaddition. The following illustration shows an example of the Sulfa-Staudinger cycloaddition. Benzylidenemethylamine reacts with ethanesulfonyl chloride to a β-sultam. For this reaction was tetrahydrofuran (THF) used as a solvent and the solution needed to rest for 24 hours.{{cite journal|last1=Yang|first1=Zhanhui|last2=Chen|first2=Ning|last3=Xu|first3=Jiaxi|title=Substituent-Controlled Annuloselectivity and Stereoselectivity in the Sulfa-Staudinger Cycloadditions|journal=The Journal of Organic Chemistry|volume=80|issue=7|year=2015|pages=3611–3620|issn=0022-3263|doi=10.1021/acs.joc.5b00312|pmid=25756543}}

File:Sulfa-Staudinger-Synthese V4.svg

Category:Name reactions

Category:Cycloadditions