Curtis D. Pfeiffer - Midland MI Nile N. Frawley - Midland MI Thomas L. Peters - Midland MI Philip J. Savickas - Midland MI David R. Albers - Midland MI Steven J. Gluck - Lake Jackson TX Lawrence W. Nicholson - Freeland MI Jose B. Esquivel H. - Midland MI
A chemical analysis method for determining chemically related differences between subject biological material such as genetically modified plant material and control biological material such as genetically unmodified plant material, which method includes at least the following six steps. The first step is to contact the subject biological material with a fluid extractant, such as a mixture of water, isopropanol and potassium hydroxide, to produce a fluid extract of the subject biological material. The second step is to contact the control biological material with the fluid extractant to produce a fluid extract of the control biological material. The third step is to chromatograph the fluid extract of the subject biological material, for example, gas or fluid chromatography, to produce a chromatogram of the fluid extract of the subject biological material. The fourth step is to chromatograph the fluid extract of the control biological material to produce a chromatogram of the fluid extract of the control biological material. The fifth step is to determine the differences between the chromatograms, for example, by using the method of U. S. Pat. No.
Asymmetric Synthesis Of .Beta.-Amino Alcohols From Chiral Or Achiral Enamines
Bakthan Singaram - Santa Cruz CA Gary B. Fisher - Boulder Creek CA Christian T. Goralski - Midland MI Lawrence W. Nicholson - Midland MI
Assignee:
The Regents of the University of California - Oakland CA
International Classification:
C07C21300 C07C21508 C07C21338 C07D20712 C07D29508
US Classification:
544170
Abstract:
The present invention relates to a process for the synthesis of chiral enantiomerically pure. beta. -amino alcohols which are extraordinarily important as therapeutic agents for the treatment of a variety of human disorders and as chiral auxiliaries in organic synthesis. The hydroboration of enamines is a versatile and convenient method for the synthesis of both racemic and enantiomerically pure. beta. -amino alcohols in high yields. This methodology enables the synthesis of virtually any. beta. -amino alcohol. Hydroboration of these enamines with chiral organic borohydrides, e. g. either mono- or diisopinocampheylborane, followed by oxidation with aqueous or solid NaOH/30% H. sub. 2 O. sub. 2 or Me. sub. 3 NO, gives the corresponding chiral. beta. -amino alcohol.
Lawrence W. Nicholson - Midland MI Christian T. Goralski - Midland MI Curtis D. Pfeiffer - Midland MI
Assignee:
The Dow Chemical Company - Midland MI
International Classification:
B01D 1508
US Classification:
210635
Abstract:
A process for separating enantiomeric mixtures by liquid chromatography using a stationary phase that includes cellulose or amylose derivative and a mobile phase that includes methanol and pentane, the concentration of methanol in the mobile phase being greater than one tenth percent by volume and less than the saturation concentration of methanol in the mobile phase, the concentration of pentane being at least that necessary to resolve the enantiomeric mixture into its enantiomers with a resolution at least one and one half times greater than the pentane of the mobile phase is replaced with hexane.
Method For Reagent Addition To A Flowing Liquid Carrier Stream
Timothy S. Stevens - Midland MI Nile N. Frawley - Midland MI Daniel J. Swart - Midland MI William C. Harris - Neshanic Station NJ Deborah E. Diedering - Sanford MI Lawrence W. Nicholson - Midland MI L. David Rothman - Midland MI
Assignee:
The Dow Chemical Company - Midland MI
International Classification:
G01N 3006 G01N 3508
US Classification:
436 52
Abstract:
An analytical chemistry apparatus and method for introducing a reagent into a flowing stream of liquid carrier in order to quantitatively analyze one or more components of a sample added into the carrier. The reagent is permeated across a short section of membrane having relatively large pores. The use of such a membrane: (a) allows the membrane to be protected from physical damage by covering it with a perforate structure; (b) significantly reduces bandspreading across the membrane reagent addition device; (c) reduces the pressure drop across the membrane reagent addition device; and (d) still allows for the permeation of an effective amount of the reagent into the carrier. The reagent is preferably pressurized to minimize leakage of carrier across the membrane and the reagent can be self-pressurized by essentially completely filling the reagent reservoir of the invention with reagent and then hermetically sealing the reservoir.
mishap, the MEU determined that the Osprey is safe to fly and resumed operations," III Marine Expeditionary Force commander Lt. Gen. Lawrence Nicholson said in a statement. "I would never put my aircrews or any local citizens in danger by flying an aircraft that I do not believe is safe and ready to fly.
Date: Aug 11, 2017
Category: World
Source: Google
US Military Osprey Crash-Lands off Okinawa, No Fatalities
Lt. Gen. Lawrence Nicholson, Okinawa area coordinator for the Marines, said the Osprey's propeller was damaged when it hit a fuel line during offshore refueling. Its pilot landed the aircraft in shallow water to avoid the danger of flying overland back to the base, he said.
In a press conference in Okinawa following the incident, Lt. Gen. Lawrence Nicholson said the aircraft had been conducting aerial refueling operations over water when the rotor blades hit the refueling line, causing damage to the aircraft.
Date: Dec 14, 2016
Category: World
Source: Google
US Marine Osprey crashes off Japan, 5 rescued, US officials say
have lost a fine American patriot who volunteered to serve for freedom," said Lt. Gen. Lawrence Nicholson, commanding general of the III Marine Expeditionary Force. "I want to sincerely thank the Japanese government for the tremendous efforts they made during search operations following the mishap.
Date: Dec 13, 2016
Category: U.S.
Source: Google
Huge protest on Okinawa opposes US military after killing
Last month, Lt. Gen. Lawrence Nicholson, the commanding general of Marine Forces Japan, stressed the importance of the bilateral alliance. Please do not allow this terrible act of violence to drive a wedge between our two communities, he said on Okinawa, referring to the womans death. There may
ncluding senior government officials. Earlier, U.S. Ambassador Caroline Kennedy was summoned to Japans Foreign Ministry to receive an official protest, and the senior U.S. military officer on Okinawa, Marine Lt. Gen. Lawrence Nicholson, traveled to the Okinawa governors office to formally apologize.
Gen. Lawrence Nicholson, the coalition's deputy chief of staff for operations, said in an interview with reporters traveling with Panetta that coalition commanders are pushing the Afghans to do more on their own. The idea is to push them "right to the brink of failure" so that they are ready to han
Date: Dec 12, 2012
Category: World
Source: Google
Afghans Urged to Take All Military Tasks Except Aviation
iation, close air support, that might be the one outlier weare still going to be involved in, U.S. Marine Corps MajorGeneral Lawrence Nicholson, the deputy chief of staff foroperations with the International Security Assistance Force,said today in Kabul. We have 24 months to get that right.