(Q44499187)

3 December 2017

Architectural self-construction in nature and chemical synthesis (English)

1 reference

3 December 2017

Erik J Sorensen

1

1 reference

PubMed ID

12837531

3 December 2017

language of work or name

English

0 references

publication date

1 July 2003

1 reference

Bioorganic & Medicinal Chemistry

3 December 2017

1 reference

3 December 2017

11

1 reference

3 December 2017

15

1 reference

3 December 2017

3225-3228

1 reference

Zur Kenntnis der Triterpene. 190. Mitteilung. Eine stereochemische Interpretation der biogenetischen Isoprenregel bei den Triterpenen

3 December 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2803%2900185-8

7 January 2021

The Stereochemistry of Polyene Cyclization

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2803%2900185-8

7 January 2021

2,3-Oxidosqualene, an Intermediate in the Biological Synthesis of Sterols from Squalene1

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2803%2900185-8

7 January 2021

Enzymic Conversion of Squalene 2,3-Oxide to Lanosterol and Cholesterol

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2803%2900185-8

7 January 2021

https://api.crossref.org/works/10.1016%2FS0968-0896%2803%2900185-8

1 reference

7 January 2021

Nonenzymic biogenetic-like olefinic cyclizations

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2803%2900185-8

7 January 2021

Biomimetic polyene cyclizations

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2803%2900185-8

7 January 2021

Nature knows best: an amazing reaction cascade is uncovered by design and discovery

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2803%2900185-8

7 January 2021

LXIII.—A synthesis of tropinone

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2803%2900185-8

7 January 2021

Die Synthese des Tropinons, Pseudopelletierins, Lobelanins und verwandter Alkaloide unter physiologischen Bedingungen

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2803%2900185-8

7 January 2021

Biomimetic synthesis of alkaloids

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2803%2900185-8

7 January 2021

Vitamin B12: Experiments Concerning the Origin of Its Molecular Structure

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2803%2900185-8

7 January 2021

A synthesis of (+)-FR182877, featuring tandem transannular Diels-Alder reactions inspired by a postulated biogenesis

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2803%2900185-8

7 January 2021

An Enantioselective Synthesis of FR182877 Provides a Chemical Rationalization of Its Structure and Affords Multigram Quantities of Its Direct Precursor

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2803%2900185-8

7 January 2021

A new antimitotic substance, FR182877. I. Taxonomy, fermentation, isolation, physico-chemical properties and biological activities.

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2803%2900185-8

7 January 2021

A new antimitotic substance, FR182877. II. The mechanism of action

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2803%2900185-8

7 January 2021

A new antimitotic substance, FR182877. III. Structure determination

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2803%2900185-8

7 January 2021

Biomimetic synthesis of (-)-longithorone A

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2803%2900185-8

7 January 2021

A cascade cycloaddition strategy leading to the total synthesis of (-)-FR182877

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2803%2900185-8

7 January 2021

Hexacyclinic acid, a Polyketide from Streptomyces with a Novel Carbon Skeleton We express our thanks to Hoechst AG (Frankfurt) for providing us with Streptomyces cellulosae (strain S 1013) and Mr. M. Decke for excellent technical assistance. We wish

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2803%2900185-8

7 January 2021

Harnessing the biosynthetic code: combinations, permutations, and mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2803%2900185-8

7 January 2021

Harnessing the Biosynthetic Potential of Modular Polyketide Synthases

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2803%2900185-8

7 January 2021

Utilization of alternate substrates by the first three modules of the epothilone synthetase assembly line

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2803%2900185-8

7 January 2021

Stereocontrolled synthesis of polyketide libraries: Boron-mediated aldol reactions with aldehydes on solid support

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2803%2900185-8

7 January 2021

A Combinatorial Approach to Polyketide-Type Libraries by Iterative Asymmetric Aldol Reactions Performed on Solid Support We thank the European Commission (TMR Network ERB-FMR XCT 96-0011 and IHP Network HPRN-CT-2000-00014), EPSRC, Pfizer, and Merck

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2803%2900185-8

7 January 2021

Building a small polypropionate library. Synthesis of all possible stereotetrads (building blocks for polyketide synthesis) from furan

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2803%2900185-8

7 January 2021

The synthesis of an exhaustively stereodiversified library of cis-1,5 enediols by silyl-tethered ring-closing metathesis

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2803%2900185-8

7 January 2021

High-affinity mu opioid receptor ligands discovered by the screening of an exhaustively stereodiversified library of 1,5-enediols

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2803%2900185-8

7 January 2021

Toward the combinatorial synthesis of polyketide libraries: asymmetric aldol reactions with alpha-chiral aldehydes on solid support

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2803%2900185-8

7 January 2021

10.1016/S0968-0896(03)00185-8

Identifiers

DOI

1 reference

3 December 2017

1 reference

PubMed ID

12837531