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1
Published in 2017 at "Acta Informatica"
DOI: 10.1007/s00236-017-0294-5
Abstract: Formal synthesis is the process of generating a program satisfying a high-level formal specification. In recent times, effective formal synthesis methods have been proposed based on the use of inductive learning. We refer to this…
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Keywords:
inductive synthesis;
formal synthesis;
inductive learning;
formal inductive ... See more keywords
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0
Published in 2019 at "Acta Informatica"
DOI: 10.1007/s00236-019-00359-1
Abstract: We present a sound and automated approach to synthesizing safe, digital controllers for physical plants represented as time-invariant models. Models are linear differential equations with inputs, evolving over a continuous state space. The synthesis precisely…
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Keywords:
synthesis provably;
safe digital;
automated formal;
digital controllers ... See more keywords
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Published in 2021 at "Organic letters"
DOI: 10.1021/acs.orglett.1c03502
Abstract: An enantioselective formal synthesis of (-)-aflatoxin B2 from 4-methoxyphenylacetic acid has been achieved by an approach that produces a key carbon-carbon bond, a benzylic stereocenter, and two arene carbon-oxygen bonds in the course of three…
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Keywords:
formal synthesis;
synthesis;
synthesis aflatoxin;
enantioselective formal ... See more keywords
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1
Published in 2017 at "Organic letters"
DOI: 10.1021/acs.orglett.7b02428
Abstract: A divergent entry to the chiral bicyclo[5.3.0]decane skeletons relevant to sesqui- and higher terpenoids has been achieved. Its usefulness was demonstrated by formal synthesis of a guaiane sesquiterpenoid (-)-englerin A. The key reactions are (i)…
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Keywords:
bicyclo;
formal synthesis;
chiral bicyclo;
nazarov cyclization ... See more keywords
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Published in 2018 at "Organic letters"
DOI: 10.1021/acs.orglett.7b03972
Abstract: Desymmetrization of a p-quinone monoacetal by organocatalytic sulfa-Michael addition provided rapid access to a C-ring building block for a formal synthesis of (-)-codeine. By means of a diastereoselective 1,2-addition for A/C-ring union, an intramolecular nitrone…
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Keywords:
codeine;
formal synthesis;
codeine application;
synthesis codeine ... See more keywords
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Published in 2019 at "Organic letters"
DOI: 10.1021/acs.orglett.9b02015
Abstract: Starting from the commercially available 4-bromoindole, a concise and efficient enantioselective formal synthesis of (+)-cycloclavine (1) in 13 steps with 2.0% overall yield and a total synthesis of (+)-5-epi-cycloclavine (2) in 14 steps with 3.3%…
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Keywords:
enantioselective formal;
cycloclavine;
synthesis cycloclavine;
formal synthesis ... See more keywords
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Published in 2017 at "ACS Omega"
DOI: 10.1021/acsomega.7b00663
Abstract: Cyclopropanation using dimethylsulfoxonium methylide (Corey–Chaykovsky reaction) was examined with a series of linear α,β-unsaturated ketones, and the results showed that the major trajectory for the addition of the sulfur ylide to the enones is anti,…
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Keywords:
unsaturated ketones;
dimethylsulfoxonium methylide;
formal synthesis;
addition ... See more keywords
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2
Published in 2023 at "Chemical communications"
DOI: 10.1039/d3cc01935g
Abstract: A unified strategy for accessing the core structure of cyathane diterpenoids has been developed, enabling the formal synthesis of (-)-erinacine B. The key feature includes an organocatalyzed asymmetric intramolecular vinylogous aldol reaction for convergently building…
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Keywords:
synthesis erinacine;
erinacine enabled;
formal synthesis;
enabled asymmetric ... See more keywords
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2
Published in 2023 at "Chemical Science"
DOI: 10.1039/d3sc00595j
Abstract: A convergent total synthesis of bacterial gyrase B/topoisomerase IV inhibitor kibdelomycin (a.k.a. amycolamicin) (1) was devised starting from inexpensive d-mannose and l-rhamnose, which were converted in new efficient ways to an N-acylated amycolose and an…
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Keywords:
kibdelomycin derivatisation;
amycolose glycosides;
synthesis kibdelomycin;
synthesis ... See more keywords
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1
Published in 2018 at "Synlett"
DOI: 10.1055/s-0036-1591880
Abstract: An efficient total synthesis of luteoalbusin A was achieved in nine linear steps and in 17% overall yield from the known and easily accessible 3a-(3-indolyl)-hexahydropyrrolo[2,3-b]indole. A formal synthesis of (+)-T988 C through manipulation of the…
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Keywords:
synthesis t988;
formal synthesis;
total synthesis;
synthesis luteoalbusin ... See more keywords
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1
Published in 2021 at "Synlett"
DOI: 10.1055/s-0040-1720383
Abstract: An asymmetric formal synthesis of trichodermamides B and C was achieved in 15 steps based on a tyrosine ester chiral-pool approach. Key features of this synthesis include stereoselective construction of a cis-1,2-oxazadecaline core by an…
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Keywords:
asymmetric formal;
synthesis trichodermamides;
formal synthesis;