Conversion of substrate analogs suggests a Michael cyclization in iridoid biosynthesis (Q42095945)

16 October 2017

Conversion of substrate analogs suggests a Michael cyclization in iridoid biosynthesis (English)

1 reference

16 October 2017

2

Fernando Geu-Flores

0 references

Sarah E. O'Connor

series ordinal

5

object named as

Sarah E O'Connor

0 references

Stefan Bräse

series ordinal

3

object named as

Stefan Bräse

1 reference

16 October 2017

Stephanie Lindner

1

1 reference

PMC publication ID

4245709

16 October 2017

Nathaniel H Sherden

series ordinal

4

1 reference

16 October 2017

23 October 2014

1 reference

16 October 2017

Chemistry and Biology

1 reference

16 October 2017

21

1 reference

16 October 2017

11

1 reference

16 October 2017

1452-1456

1 reference

Vinylogous chain branching catalysed by a dedicated polyketide synthase module

16 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4245709

An alternative route to cyclic terpenes by reductive cyclization in iridoid biosynthesis

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4245709

Structure and function of ∆1-tetrahydrocannabinolic acid (THCA) synthase, the enzyme controlling the psychoactivity of Cannabis sativa

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4245709

Current developments and challenges in the search for a naturally selected Diels-Alderase

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4245709

Naturally occurring iridoids and secoiridoids. An updated review, part 4.

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4245709

The family of terpene synthases in plants: a mid-size family of genes for specialized metabolism that is highly diversified throughout the kingdom

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4245709

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4245709

Monoterpene and sesquiterpene synthases and the origin of terpene skeletal diversity in plants

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4245709

Biological and pharmacological activities of iridoids: recent developments

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4245709

The crystal structure of progesterone 5beta-reductase from Digitalis lanata defines a novel class of short chain dehydrogenases/reductases

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4245709

Truncation of N-terminal regions of Digitalis lanata progesterone 5β-reductase alters catalytic efficiency and substrate preference

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4245709

Highly conserved progesterone 5 beta-reductase genes (P5 beta R) from 5 beta-cardenolide-free and 5 beta-cardenolide-producing angiosperms.

17 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4245709

Polyketide-chain branching by an enzymatic Michael addition

17 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4245709

The hetero-Diels-Alder addition of sulfur dioxide to 1-fluorobuta-1,3-dienes: the sofa conformations preferred by 6-fluorosultines (6-fluoro-3,6-dihydro-1,2-oxathiin-2-oxides) enjoy enthalpic and conformational Anomeric effects

17 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4245709

Selective fluoroalkylation of organic compounds by tackling the "negative fluorine effect"

17 August 2018

1 reference

12 December 2020

Crossed intramolecular Rauhut-Currier-type reactions via dienamine activation

1 reference

12 December 2020

Reconstitution of a fungal meroterpenoid biosynthesis reveals the involvement of a novel family of terpene cyclases

1 reference

12 December 2020

Catalytic asymmetric reductive Michael cyclization

1 reference

12 December 2020

New Organic Chemistry of Sulfur Dioxide

1 reference

12 December 2020

Bacterial Synthesis of Diverse Indole Terpene Alkaloids by an Unparalleled Cyclization Sequence

1 reference

12 December 2020

Mechanism for iridane skeleton formation from acyclic monoterpenes in the biosynthesis of secologanin and vindoline in Catharanthus roseus and Lonicera morrowii.

1 reference

12 April 2024

https://opencitations.net/index/api/v1/citations/10.1248/CPB.32.1671

Mechanism of iridane skeleton formation in the biosynthesis of iridoid glucosides in Gardenia jasminoides cell cultures.

1 reference

12 April 2024

https://opencitations.net/index/api/v1/citations/10.1248/CPB.31.4185

Identifiers

DOI

10.1016/J.CHEMBIOL.2014.09.010

1 reference

16 October 2017

1 reference

PMC publication ID

4245709

16 October 2017

PubMed publication ID

25444551

1 reference

PMC publication ID

4245709