Highly regio- and stereoselective phosphinylphosphination of terminal alkynes with tetraphenyldiphosphine monoxide under radical conditions

• Dat Phuc Tran,
• Yuki Sato,
• Yuki Yamamoto,
• Shin-ichi Kawaguchi,
• Shintaro Kodama,
• Akihiro Nomoto and
• Akiya Ogawa

Beilstein J. Org. Chem. 2021, 17, 866–872, doi:10.3762/bjoc.17.72

• reactivities. The method using V-40 as an initiator is successfully investigated for the regio- and stereoselective phosphinylphosphination of terminal alkynes giving the corresponding trans-isomers of 1-diphenylphosphinyl-2-diphenylthiophosphinyl-1-alkenes in good yields. The protocol can be applied to a wide

• variety of terminal alkynes including both alkyl- and arylalkynes. Keywords: (E)-1,2-bis(diphenylphosphino)ethylene derivative; radical addition; stereoselective phosphinylphosphination; terminal alkyne; tetraphenyldiphosphine monoxide; Introduction Organophosphorus compounds are an essential class of

• A1. Radical A1 is captured by Ph2P(O)PPh2 to provide A2, regio- and stereoselectively [62]. Conclusion In conclusion, a highly regio- and stereoselective phosphinylphosphination of alkynes with Ph2P(O)PPh2 has been successfully developed. The radical initiator V-40 can be used to selectively generate

Stereoselective syntheses of 3-aminocyclooctanetriols and halocyclooctanetriols

• Emine Salamci and
• Yunus Zozik

Beilstein J. Org. Chem. 2021, 17, 705–710, doi:10.3762/bjoc.17.59

The synthesis of chiral β-naphthyl-β-sulfanyl ketones via enantioselective sulfa-Michael reaction in the presence of a bifunctional cinchona/sulfonamide organocatalyst

• Deniz Tözendemir and
• Cihangir Tanyeli

Beilstein J. Org. Chem. 2021, 17, 494–503, doi:10.3762/bjoc.17.43

• naturally occurring cinchona alkaloids have shown remarkable performance as organocatalysts for stereoselective synthesis in the past decade [1][2][3][4][5][6]. Among them, quinine-derived organocatalysts make a noteworthy appearance in the formation of new stereogenic centres, which can serve as valuable

Synthetic strategies of phosphonodepsipeptides

• Jiaxi Xu

Beilstein J. Org. Chem. 2021, 17, 461–484, doi:10.3762/bjoc.17.41

• phosphonodepsipeptides in the future. However, highly stereoselective asymmetric synthetic methods of phosphonodepsipeptides are of high demand and need to be developed in the near future. Phosphonopeptides, phosphonodepsipeptides, peptides, and depsipeptides. The diverse strategies for phosphonodepsipeptide synthesis

Synthesis of legonmycins A and B, C(7a)-hydroxylated bacterial pyrrolizidines

• Wilfred J. M. Lewis,
• David M. Shaw and
• Jeremy Robertson

Beilstein J. Org. Chem. 2021, 17, 334–342, doi:10.3762/bjoc.17.31

• might be thought to be theoretically possible [18][19], via a late-stage addition to an intact pyrrolizidine core. The molecules are isolated as their racemates and, by analogy to the clazamycins, even if the LgnC-mediated hydroxylation is fully stereoselective, the C(7a) center is expected to be

Diels–Alder reaction of β-fluoro-β-nitrostyrenes with cyclic dienes

• Savva A. Ponomarev,
• Roman V. Larkovich,
• Alexander S. Aldoshin,
• Andrey A. Tabolin,
• Sema L. Ioffe,
• Jonathan Groß,
• Till Opatz and
• Valentine G. Nenajdenko

Beilstein J. Org. Chem. 2021, 17, 283–292, doi:10.3762/bjoc.17.27

• one of the most widely used fluorine-containing building blocks [48][49]. Recently, we have developed an efficient stereoselective synthesis of β-fluoro-β-nitrostyrenes 1 based on the radical nitration of 2-bromo-2-fluorostyrenes [50]. This process takes place with simultaneous elimination of bromine

The preparation and properties of 1,1-difluorocyclopropane derivatives

• Kymbat S. Adekenova,
• Peter B. Wyatt and
• Sergazy M. Adekenov

Beilstein J. Org. Chem. 2021, 17, 245–272, doi:10.3762/bjoc.17.25

• stereoselective methods for the synthesis and transformations of cyclopropane derivatives. These investigations gained a significant interest, because cyclopropane and cyclopropene fragments are present in the structures of many biologically active substances, such as antibiotics, anticancer, and antimycotic

• intermediate allylic cation which was the electrophile in a Friedel–Crafts reaction with 159. The subsequent desilylation of the Friedel–Crafts product gave an α-fluorinated ketone intermediate which then reacted with a second equivalent of 159 in a (Z)-stereoselective, chelation-controlled process. Fu et al

A sustainable strategy for the straightforward preparation of 2H-azirines and highly functionalized NH-aziridines from vinyl azides using a single solvent flow-batch approach

• Michael Andresini,
• Leonardo Degannaro and
• Renzo Luisi

Beilstein J. Org. Chem. 2021, 17, 203–209, doi:10.3762/bjoc.17.20

• preparation of 2H-azirines and their stereoselective transformation into highly functionalized NH-aziridines, starting from vinyl azides and organolithium compounds. The protocol has been developed using cyclopentyl methyl ether (CPME) as an environmentally benign solvent, resulting into a sustainable, safe

Au(III) complexes with tetradentate-cyclam-based ligands

• Ann Christin Reiersølmoen,
• Thomas N. Solvi and
• Anne Fiksdahl

Beilstein J. Org. Chem. 2021, 17, 186–192, doi:10.3762/bjoc.17.18

• trans product. Thus, the proper choice of the gold catalyst allows highly stereoselective formation of either cis or trans cyclopropanation products and facilitates the isolation of pure isomers. Despite the chiral nature of these ligands, no enantioselectivity was observed in the test reactions

Progress in the total synthesis of inthomycins

• Bidyut Kumar Senapati

Beilstein J. Org. Chem. 2021, 17, 58–82, doi:10.3762/bjoc.17.7

• . Therefore, the synthesis of inthomycin A was advanced in the racemic form. Treatment of compound (rac)-17 with aqueous ammonia gave the corresponding amide (rac)-18 in 96% yield. Heck coupling between (rac)-18 and vinylboronate pinacol ester [31] using Pd(PPh3)4/Et3N conditions provided stereoselective

• (rac)-13 in a stereoselective manner, attention was then focused on the development of an analogous strategy towards the (Z,Z,E)- and (Z,E,E)-triene systems present in oxazolomycin A (5a) and oxazolomycin C (5c), respectively. The key steps were i) synthesis of dienyl halides, ii) synthesis of the

• mixture of (Z,E)/(E,E)-36a, respectively). Aldehyde 35 was then converted into dibromide 37 using PPh3/CBr4 followed by stereoselective palladium-catalyzed monoreduction according to the literature available protocol [41] to give vinyl bromide 38 in 76% yield (Z/E as 99:1 mixture). Iodide 15a [42] was

Silver-catalyzed synthesis of β-fluorovinylphosphonates by phosphonofluorination of aromatic alkynes

• Yajing Zhang,
• Qingshan Tian,
• Guozhu Zhang and
• Dayong Zhang

Beilstein J. Org. Chem. 2020, 16, 3086–3092, doi:10.3762/bjoc.16.258

• stereoselective manner under mild reaction conditions. This reaction is operationally simple and offers an excellent functional group tolerance as well as a broad substrate scope that includes both terminal and internal alkynes. The reaction proceeded through the oxidative generation of a P-centered radical and

• others concerning the silver-catalyzed phosphonofluorination of alkenes [24][25][26], we herein present a general silver-catalyzed regio- and stereoselective phosphonofluorination of alkynes using Selectfluor® and phosphonates as reactants (Scheme 1). This new silver-catalyzed approach to fluorinated

All-carbon [3 + 2] cycloaddition in natural product synthesis

• Zhuo Wang and
• Junyang Liu

Beilstein J. Org. Chem. 2020, 16, 3015–3031, doi:10.3762/bjoc.16.251

• selectively attacked the C-8 ketone moiety of 47 to give alcohol 49 in β-configuration in 80% yield [32]. Chemoselective and stereoselective reduction of the C-9 ketone of 49 was accomplished by treatment with NaBH(OAc)3 [33] and produced 50 after a two-step synthesis. Removal of the sulfoximine group in 50

• ] cycloadditions, which are usually under substrate-control. Remarkable innovation of the stereoselective palladium-catalyzed trimethylenemethane cycloaddition reported by Trost’s group, which makes use of catalytic amounts of palladium and chiral phosphine ligand 74, was applied successfully in the

Vicinal difluorination as a C=C surrogate: an analog of piperine with enhanced solubility, photostability, and acetylcholinesterase inhibitory activity

• Yuvixza Lizarme-Salas,
• Alexandra Daryl Ariawan,
• Ranjala Ratnayake,
• Hendrik Luesch,
• Angela Finch and
• Luke Hunter

Beilstein J. Org. Chem. 2020, 16, 2663–2670, doi:10.3762/bjoc.16.216

• for E-alkenes in medicinal chemistry. Keywords: Alzheimer's disease; bioisostere; conformational analysis; gauche effect; stereoselective synthesis; Introduction Piperine (1, Figure 1) is a well-known natural product that is derived from peppercorns [1][2][3]. Many biological studies of 1 have been

• . Stereoselective fluorination is an emerging strategy for controlling the conformations of organic molecules. The highly polarized C–F bond tends to align in predictable ways with adjacent functional groups, due to a combination of hyperconjugative and/or dipolar interactions [18][19][20][21]. This knowledge led

Hierarchically assembled helicates as reaction platform – from stoichiometric Diels–Alder reactions to enamine catalysis

• David Van Craen,
• Jenny Begall,
• Johannes Großkurth,
• Leonard Himmel,
• Oliver Linnenberg,
• Elisabeth Isaak and
• Markus Albrecht

Beilstein J. Org. Chem. 2020, 16, 2338–2345, doi:10.3762/bjoc.16.195

• Fujita et al. [9][10][11] or stereoselective nucleophilic substitutions by Raymond et al. [12] are important examples in this context. Recently, we described the use of hierarchically assembled helicates as templates for stereoselective Diels–Alder reactions via a post-functionalization process [13

• off the stereoselectivity [13]. Herein we investigated the induction pathway and significantly optimized the stereoselectivity of the reaction. Furthermore, a catalytic approach was introduced which paves the way to the final goal of supramolecular stereoselective catalysis with hierarchical helicates

• as homogeneous catalysts. Results and Discussion Stereoselective Diels–Alder reactions in the periphery of hierarchically assembled helicates Elucidating the induction pathway of the Diels–Alder reaction is vital for the optimization of the system described above and for the development of future

Synthetic approaches to bowl-shaped π-conjugated sumanene and its congeners

• Shakeel Alvi and
• Rashid Ali

Beilstein J. Org. Chem. 2020, 16, 2212–2259, doi:10.3762/bjoc.16.186

• sumanene (2), it is not only gifted with three benzylic positions stapled between the benzene rings of the triphenylene system but also possess the bowl-curvature which enables stereoselective functionalization at these valuable positions. Taking the advantage of these benzylic positions, two years later

• the trideuteriosumanene 33 in a stereoselective manner from the same trianion 31 just by trapping it with CD3OD/CH3OD (Scheme 5). In the same paper, they have also reported the hexaallylated sumanene 34 as well as hexa-p-methoxybenzylsumanene 35 by reacting sumanene (2) with allyl bromide and 4

• mono-substituted sumanene derivatives 49b–d in a stereoselective manner as can be inspected from Scheme 10 [41][42]. In another event, Amaya, Ito, Katoh and Hirao reported a vital building block 53 to extend the π-conjugation bidirectionally through regioselective functionalization (Scheme 11) [43]. To

Reactions of 3-aryl-1-(trifluoromethyl)prop-2-yn-1-iminium salts with 1,3-dienes and styrenes

• Thomas Schneider,
• Michael Keim,
• Bianca Seitz and
• Gerhard Maas

Beilstein J. Org. Chem. 2020, 16, 2064–2072, doi:10.3762/bjoc.16.173

• -(1-phenylvinyl)indene 12 through an intramolecular iminium ion-induced 1,5-cyclization. The same cyclization type together with oxidative aromatization converts dihydronaphthalenes 16 into benzo[a]fluorenes 13. The stereochemistry of 12d can be explained by a stereoselective formation of trans-3,4

Syntheses of spliceostatins and thailanstatins: a review

• William A. Donaldson

Beilstein J. Org. Chem. 2020, 16, 1991–2006, doi:10.3762/bjoc.16.166

• strategies that rely on the generation of the C-14 stereocenter by stereoselective C–N bond formation. The Jacobsen group utilized an asymmetric Cr(III)-catalyzed cycloaddition reaction [27] between (2Z,4E)-3-(triethylsilyloxy)-2,4-hexadiene (40) and the aldehyde 41 to generate the 4-silyloxydihydropyran 43

• cleavage of the secondary triisopropylsilyl ether were prerequisites for a vanadium-catalyzed stereoselective epoxidation of the exocyclic double bond to give 90. The C-4 hydroxy group was eventually protected as a triethylsilyl ether. Through abortive attempts, Jacobsen found that the generation of the

• with a 6:1 diastereoselectivity. The Red-Al reduction of 94, protection of the 2° alcohol, and reduction of the enoate to an allylic alcohol were prerequisites for the stereoselective 2,3-sigmatropic selenoxide rearrangement to generate 95. Further protecting group manipulation and Johnson–Lemieux

Stereoselective Biginelli-like reaction catalyzed by a chiral phosphoric acid bearing two hydroxy groups

• Xiaoyun Hu,
• Jianxin Guo,
• Cui Wang,
• Rui Zhang and
• Victor Borovkov

Beilstein J. Org. Chem. 2020, 16, 1875–1880, doi:10.3762/bjoc.16.155

• To develop new efficient stereoselective catalysts for Biginelli-like reactions, a chiral phosphoric acid bearing two hydroxy groups derived from ʟ-tartaric acid was successfully synthesized via highly regioselective transformations of enantiopure 1,1,4,4-tetraphenylbutanetetraol. The obtained

• ) H bondings with the enolizable ketone, respectively. This rigid chiral transition-state structure favored the stereoselective attack of the enol on the imine. Once the two hydroxy groups were etherified, the loss of the rigid structure would lead to low enantioselectivity. Additionally, this

Synthesis of the tetrasaccharide repeating unit of the O-specific polysaccharide of Azospirillum doebereinerae type strain GSF71^T using linear and one-pot iterative glycosylations

• Arin Gucchait,
• Pradip Shit and
• Anup Kumar Misra

Beilstein J. Org. Chem. 2020, 16, 1700–1705, doi:10.3762/bjoc.16.141

• the O-specific polysaccharide of Azospirillum doebereinerae type strain GSF71T in a very good yield adopting sequential glycosylation followed by removal of the p-methoxybenzyl (PMB) group in the same pot. Further, the synthetic strategy was modified by carrying out three stereoselective iterative

• elongation C-3 hydroxy group in the ʟ-rhamnosyl thioglycoside donor 3 allowed carrying out the stereoselective glycosylation steps followed by the removal of the PMB group [25] in one pot. This was achieved by using a combination [26][27][28][29][30] of N-iodosuccinimide (NIS) and perchloric acid supported

• repeating unit of the polysaccharide (Figure 1). The stereoselective glycosylation of compound 2 with ʟ-rhamnosyl thioglycoside 3 in the presence of a combination of NIS and HClO4-SiO2 [26][27] followed by removal of the PMB group [25] from the product in the same pot by tuning of the reaction conditions

Pauson–Khand reaction of fluorinated compounds

• Jorge Escorihuela,
• Daniel M. Sedgwick,
• Alberto Llobat,
• Mercedes Medio-Simón,
• Pablo Barrio and
• Santos Fustero

Beilstein J. Org. Chem. 2020, 16, 1662–1682, doi:10.3762/bjoc.16.138

• quantities of cobalt present in the reaction mixture. The same group also studied the intramolecular PKR of chiral fluorine-containing N-tethered 1,7-enynes 48 for the stereoselective construction of enantioenriched bicyclic alkaloid analogues 49, containing a fluorine atom in the bridge position [61]. For

Azidophosphonium salt-directed chemoselective synthesis of (E)/(Z)-cinnamyl-1H-triazoles and regiospecific access to bromomethylcoumarins from Morita–Baylis–Hillman adducts

• Soundararajan Karthikeyan,
• Radha Krishnan Shobana,
• Kamarajapurathu Raju Subimol,
• J. Helen Ratna Monica and
• Ayyanoth Karthik Krishna Kumar

Beilstein J. Org. Chem. 2020, 16, 1579–1587, doi:10.3762/bjoc.16.130

• transformations employed quaternary phosphonium salts as favourable catalysts [36]. Their synthetic utility was not only confined to catalysis, but they were also used as intermediates for the synthesis of 1H-indazoles [37], as promoters for stereoselective rearrangements [38], and as temporary protectors of O,P

An overview on disulfide-catalyzed and -cocatalyzed photoreactions

• Yeersen Patehebieke

Beilstein J. Org. Chem. 2020, 16, 1418–1435, doi:10.3762/bjoc.16.118

• . In 1996, Burton and co-workers reported the stereoselective synthesis of cis-1,2-difluorotriethylsilyethylene and its conversion to a variety of cis-1,2-difluoroethylene synthons, which are important building blocks in the preparation of fluorine-containing pharmaceuticals, polymers, and bioactive

Recent synthesis of thietanes

• Jiaxi Xu

Beilstein J. Org. Chem. 2020, 16, 1357–1410, doi:10.3762/bjoc.16.116

• ) reacted with electron-poor olefins, such as acrylonitrile (187b), methyl acrylate (187c), and cis- and trans-1,2-dichloroethenes 188, under photochemical conditions, giving 2-silylthietanes 317 and 318 in a regio- and highly stereoselective manner. However, silyl thietanes without any regio- or

Distinctive reactivity of N-benzylidene-[1,1'-biphenyl]-2-amines under photoredox conditions

• Shrikant D. Tambe,
• Kwan Hong Min,
• Naeem Iqbal and
• Eun Jin Cho

Beilstein J. Org. Chem. 2020, 16, 1335–1342, doi:10.3762/bjoc.16.114

• . The developed method can be employed for the synthesis of various bulky vicinal diamines, which are potential ligands in stereoselective synthesis. Keywords: 1,2-diamine; diversity; imine; photocatalysis; visible light; Introduction The selective formation of distinct valuable compounds from the

• applications as core structures in a variety of natural products, pharmaceuticals, and agrochemicals [34][35][36][37][38] and are valuable ligands [39][40] in stereoselective organic synthesis. Despite the availability of a plethora of synthetic methods for 1,2-diamines [41][42][43][44][45], the reported

• electron density or position of the substituent on the benzylidene moiety. Interestingly, the homocoupling process was highly stereoselective, resulting in the formation of only one diastereomer, probably due to the bulky substitution pattern of the substrates. The structure of the homocoupled 1,2-diamine

Highly selective Diels–Alder and Heck arylation reactions in a divergent synthesis of isoindolo- and pyrrolo-fused polycyclic indoles from 2-formylpyrrole

• Carlos H. Escalante,
• Eder I. Martínez-Mora,
• Carlos Espinoza-Hicks,
• Alejandro A. Camacho-Dávila,
• Fernando R. Ramos-Morales,
• Francisco Delgado and
• Joaquín Tamariz

Beilstein J. Org. Chem. 2020, 16, 1320–1334, doi:10.3762/bjoc.16.113

• Chihuahua, Circuito Universitario S/N, 31125 Chihuahua, Chih., Mexico Unidad de Servicios de Apoyo en Resolución Analítica, Universidad Veracruzana, Luis Castelazo Ayala S/N, 91190 Xalapa, Ver., Mexico 10.3762/bjoc.16.113 Abstract A highly regio-, chemo- and stereoselective divergent synthesis of isoindolo

• aromatization of the polycyclic intermediates provides the corresponding polycyclic pyrrolo-isoindoles and isoindolo-pyrrolo-indoles. A theoretical study on the stereoselective Diels–Alder reactions, carried out by calculating the endo/exo transition states, revealed the assistance of non-covalent interactions

• (Supporting Information File 1, Table S1). Hence, the latter dienes should be more reactive than diene 8b, and consequently more stereoselective [54][55][56]. In contrast, the Gibbs energy for the diene/dienophile 8c/7b (88.8:11.2) did not completely match the experimental endo/exo (99:1) ratio, but the ZPE