Daniel Martin Allwood

Dr. Daniel Martin Allwood

orcid

Research Focus & Metrics

Academic Career Length

15Years (2012-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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8 February 2016 in Nature Chemistry
Verified
Journal Article
Open access
CBClaudio Battilocchio
Claudio Battilocchio
FFFlorian Feist
Florian Feist
AHAndreas Hafner
Andreas Hafner
MSMeike Simon
Meike Simon
DTDuc N. Tran
Duc N. Tran
SLSteven V. Ley
Steven V. Ley
The ability to form multiple carbon–carbon bonds in a controlled sequence represents an important goal in modern chemical synthesis. Here, the in situ preparation of reactive allylic and benzylic boronic acids, obtained by reacting flow-generated diazo compounds with boronic acids, and their application in controlled iterative C–C bond forming reactions is described.

4 December 2013 in The Journal of Organic Chemistry
Verified
Journal Article
Closed access
DADaniel Martin Allwood
Daniel Martin Allwood
DBDavid C. Blakemore
David C. Blakemore
ABAlan D. Brown
Alan D. Brown
SLSteven V. Ley
Steven V. Ley

12 May 2014 in Organic Letters
Verified
Journal Article
Closed access
DADaniel Martin Allwood
Daniel Martin Allwood
DBDavid C. Blakemore
David C. Blakemore
SLSteven V. Ley
Steven V. Ley

ACAndrew J. Chappell
Andrew J. Chappell
DADaniel Martin Allwood
Daniel Martin Allwood
RJRebecca Johns
Rebecca Johns
SBSamantha Brown
Samantha Brown
KSKiran Sultana
Kiran Sultana
TSTrevor Simper
Trevor Simper
Use of supplements to aid performance is common practice amongst recreationally active individuals, including those without a sufficient evidence base. This investigation sought to assess whether acute supplementation with 8 g of citrulline malate (CM) (1.11: 1 ratio) would improve anaerobic performance. A randomised double blind placebo control trial was employed, using a counterbalanced design. We recruited recreationally active men and women to take part in an isokinetic chair protocol, based on German Volume Training (GVT) whereby participants attempted to perform 10 sets of 10 repetitions against a force representing 70% of their peak concentric force. The number of repetitions achieved over the course of the GVT was 94.0 ± 7.9 and 90.9 ± 13.9 for placebo and CM respectively. There was no significant difference between the placebo and CM treatment for number of repetitions (P = 0.33), isometric (P = 0.60), concentric (P = 0.38), or eccentric (P = 0.65) peak force following the GVT. Total muscle soreness was significantly higher in the CM compared to the placebo treatment following the GVT protocol over 72 h (P = 0.01); although this was not accompanied by a greater workload/number of repetitions in the CM group. We conclude that an acute dose of CM does not significantly affect anaerobic performance using an isokinetic chair in recreational active participants. Practical implications include precaution in recommending CM supplementation. Coaches and athletes should be aware of the disparity between the chemical analyses of the products reviewed in the present investigation versus the manufacturers’ claims.

27 January 2012 in ACS Medicinal Chemistry Letters
Verified
Journal Article
Closed access
TBThomas M. Beale
Thomas M. Beale
DADaniel Martin Allwood
Daniel Martin Allwood
ABAndreas Bender
Andreas Bender
PBPeter Bond
Peter Bond
JBJames D. Brenton
James D. Brenton
JXJian Xian
Jian Xian

22 August 2014 in The Journal of Organic Chemistry
Verified
Journal Article
Closed access
RMRohan R. Merchant
Rohan R. Merchant
DADaniel Martin Allwood
Daniel Martin Allwood
DBDavid C. Blakemore
David C. Blakemore
SLSteven V. Ley
Steven V. Ley