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  2. Green chemistry - Wikipedia

    en.wikipedia.org/wiki/Green_chemistry

    Green chemistry, similar to sustainable chemistry or circular chemistry, [1] is an area of chemistry and chemical engineering focused on the design of products and processes that minimize or eliminate the use and generation of hazardous substances. [2]

  3. Green solvent - Wikipedia

    en.wikipedia.org/wiki/Green_solvent

    Green solvents are environmentally friendly chemical solvents that are used as a part of green chemistry. They came to prominence in 2015, when the UN defined a new sustainability -focused development plan based on 17 sustainable development goals, recognizing the need for green chemistry and green solvents for a more sustainable future. [ 1 ]

  4. California Green Chemistry Initiative - Wikipedia

    en.wikipedia.org/wiki/California_Green_Chemistry...

    Green chemistry is the design of chemical products and processes that reduce or eliminate the use and generation of hazardous substances. [1] Green chemistry is based upon twelve principles, identified in “Green Chemistry: Theory and Practice” and adopted by the US Environmental Protection Agency (EPA). [2]

  5. tert-Butanesulfinamide - Wikipedia

    en.wikipedia.org/wiki/Tert-Butanesulfinamide

    tert-Butanesulfinamide (also known as 2-methyl-2-propanesulfinamide or Ellman's sulfinamide) is an organosulfur compound and a member of the class of sulfinamides.Both enantiomeric forms are commercially available and are used in asymmetric synthesis as chiral auxiliaries, often as chiral ammonia equivalents for the synthesis of amines.

  6. Enders SAMP/RAMP hydrazone-alkylation reaction - Wikipedia

    en.wikipedia.org/wiki/Enders_SAMP/RAMP_hydrazone...

    The Enders SAMP/RAMP hydrazone alkylation begins with the synthesis of the hydrazone from a N,N-dialkylhydrazine and a ketone or aldehyde [14]. The hydrazone is then deprotonated on the α-carbon position by a strong base, such as lithium diisopropylamide (LDA), leading to the formation of a resonance stabilized anion - an azaenolate.

  7. Green leaf volatiles - Wikipedia

    en.wikipedia.org/wiki/Green_leaf_volatiles

    Green leaf volatiles (GLV) are organic compounds released by plants. [1] Some of these chemicals function as signaling compounds between either plants of the same species, of other species, or even different lifeforms like insects.

  8. Protecting group - Wikipedia

    en.wikipedia.org/wiki/Protecting_group

    The procedure begins actually with redox chemistry at the protected phosphorus atom. A tricoordinate phosphorus, used on account of the high reactivity, is tagged with a cyanoethyl protecting group on a free oxygen. After the coupling step follows an oxidation to phosphate, whereby the protecting group stays attached.

  9. Chemiluminescence - Wikipedia

    en.wikipedia.org/wiki/Chemiluminescence

    The common colors for the light emitted by these animals are blue and green because they have shorter wavelengths than red and can transmit more easily in water. In April 2020, researchers reported having genetically engineered plants glow much brighter than previously possible by inserting genes of the bioluminescent mushroom Neonothopanus nambi .